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overflow: hidden; text-overflow: ellipsis; -webkit-line-clamp: 3; -webkit-box-orient: vertical; }</style><div class="col-xs-12 clearfix"><div class="u-floatLeft"><h1 class="PageHeader-title u-m0x u-fs30">Oxylipins</h1><div class="u-tcGrayDark">16 Followers</div><div class="u-tcGrayDark u-mt2x">Recent papers in <b>Oxylipins</b></div></div></div></div></div></div><div class="TabbedNavigation"><div class="container"><div class="row"><div class="col-xs-12 clearfix"><ul class="nav u-m0x u-p0x list-inline u-displayFlex"><li class="active"><a href="https://www.academia.edu/Documents/in/Oxylipins">Top Papers</a></li><li><a href="https://www.academia.edu/Documents/in/Oxylipins/MostCited">Most Cited Papers</a></li><li><a href="https://www.academia.edu/Documents/in/Oxylipins/MostDownloaded">Most Downloaded Papers</a></li><li><a href="https://www.academia.edu/Documents/in/Oxylipins/MostRecent">Newest Papers</a></li><li><a class="" href="https://www.academia.edu/People/Oxylipins">People</a></li></ul></div><style type="text/css">ul.nav{flex-direction:row}@media(max-width: 567px){ul.nav{flex-direction:column}.TabbedNavigation li{max-width:100%}.TabbedNavigation li.active{background-color:var(--background-grey, #dddde2)}.TabbedNavigation li.active:before,.TabbedNavigation li.active:after{display:none}}</style></div></div></div><div class="container"><div class="row"><div class="col-xs-12"><div class="u-displayFlex"><div class="u-flexGrow1"><div class="works"><div class="u-borderBottom1 u-borderColorGrayLighter"><div class="clearfix u-pv7x u-mb0x js-work-card work_79873903" data-work_id="79873903" itemscope="itemscope" itemtype="https://schema.org/ScholarlyArticle"><div class="header"><div class="title u-fontSerif u-fs22 u-lineHeight1_3"><a class="u-tcGrayDarkest js-work-link" href="https://www.academia.edu/79873903/The_nexus_between_growth_and_defence_signalling_auxin_and_cytokinin_modulate_plant_immune_response_pathways">The nexus between growth and defence signalling: auxin and cytokinin modulate plant immune response pathways</a></div></div><div class="u-pb4x u-mt3x"><div class="summary u-fs14 u-fw300 u-lineHeight1_5 u-tcGrayDarkest"><div class="summarized">Plants deploy a finely tuned balance between growth and defence responses for better fitness. Crosstalk between defence signalling hormones such as salicylic acid (SA) and jasmonates (JAs) as well as growth regulators plays a significant... <a class="more_link u-tcGrayDark u-linkUnstyled" data-container=".work_79873903" data-show=".complete" data-hide=".summarized" data-more-link-behavior="true" href="#">more</a></div><div class="complete hidden">Plants deploy a finely tuned balance between growth and defence responses for better fitness. Crosstalk between defence signalling hormones such as salicylic acid (SA) and jasmonates (JAs) as well as growth regulators plays a significant role in mediating the trade-off between growth and defence in plants. Here, we specifically discuss how the mutual antagonism between the signalling of auxin and SA impacts on plant growth and defence. Furthermore, the synergism between auxin and JA benefits a class of plant pathogens. JA signalling also poses growth cuts through auxin. We discuss how the effect of cytokinins (CKs) is multifaceted and is effective against a broad range of pathogens in mediating immunity. The synergism between CKs and SA promotes defence against biotrophs. Reciprocally, SA inhibits CK-mediated growth responses. Recent reports show that CKs promote JA responses; however, in a feedback loop, JA suppresses CK responses. We also highlight crosstalk between auxin and CKs ...</div></div></div><ul class="InlineList u-ph0x u-fs13"><li class="InlineList-item logged_in_only"><div class="share_on_academia_work_button"><a class="academia_share Button Button--inverseBlue Button--sm js-bookmark-button" data-academia-share="Work/79873903" data-share-source="work_strip" data-spinner="small_white_hide_contents"><i class="fa fa-plus"></i><span class="work-strip-link-text u-ml1x" data-content="button_text">Bookmark</span></a></div></li><li class="InlineList-item"><div class="download"><a id="a9e5c1cbede45e8398519c3cd389d995" rel="nofollow" data-download="{"attachment_id":86442474,"asset_id":79873903,"asset_type":"Work","always_allow_download":false,"track":null,"button_location":"work_strip","source":null,"hide_modal":null}" class="Button Button--sm Button--inverseGreen js-download-button prompt_button doc_download" href="https://www.academia.edu/attachments/86442474/download_file?st=MTczMjQ1MjUxNyw4LjIyMi4yMDguMTQ2&s=work_strip"><i class="fa fa-arrow-circle-o-down fa-lg"></i><span class="u-textUppercase u-ml1x" data-content="button_text">Download</span></a></div></li><li class="InlineList-item"><ul class="InlineList InlineList--bordered u-ph0x"><li class="InlineList-item InlineList-item--bordered"><span class="InlineList-item-text">by <span itemscope="itemscope" itemprop="author" itemtype="https://schema.org/Person"><a class="u-tcGrayDark u-fw700" data-has-card-for-user="163124134" href="https://karachi.academia.edu/MNaseem">Muhammad Naseem</a><script data-card-contents-for-user="163124134" type="text/json">{"id":163124134,"first_name":"Muhammad","last_name":"Naseem","domain_name":"karachi","page_name":"MNaseem","display_name":"Muhammad Naseem","profile_url":"https://karachi.academia.edu/MNaseem?f_ri=3243133","photo":"https://0.academia-photos.com/163124134/81879771/70478224/s65_muhammad.naseem.jpeg"}</script></span></span></li><li class="js-paper-rank-work_79873903 InlineList-item InlineList-item--bordered hidden"><span class="js-paper-rank-view hidden u-tcGrayDark" data-paper-rank-work-id="79873903"><i class="u-m1x fa fa-bar-chart"></i><strong class="js-paper-rank"></strong></span><script>$(function() { new Works.PaperRankView({ workId: 79873903, container: ".js-paper-rank-work_79873903", }); 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Crosstalk between defence signalling hormones such as salicylic acid (SA) and jasmonates (JAs) as well as growth regulators plays a significant role in mediating the trade-off between growth and defence in plants. Here, we specifically discuss how the mutual antagonism between the signalling of auxin and SA impacts on plant growth and defence. Furthermore, the synergism between auxin and JA benefits a class of plant pathogens. JA signalling also poses growth cuts through auxin. We discuss how the effect of cytokinins (CKs) is multifaceted and is effective against a broad range of pathogens in mediating immunity. The synergism between CKs and SA promotes defence against biotrophs. Reciprocally, SA inhibits CK-mediated growth responses. Recent reports show that CKs promote JA responses; however, in a feedback loop, JA suppresses CK responses. We also highlight crosstalk between auxin and CKs ...","downloadable_attachments":[{"id":86442474,"asset_id":79873903,"asset_type":"Work","always_allow_download":false}],"ordered_authors":[{"id":163124134,"first_name":"Muhammad","last_name":"Naseem","domain_name":"karachi","page_name":"MNaseem","display_name":"Muhammad Naseem","profile_url":"https://karachi.academia.edu/MNaseem?f_ri=3243133","photo":"https://0.academia-photos.com/163124134/81879771/70478224/s65_muhammad.naseem.jpeg"}],"research_interests":[{"id":5541,"name":"Plant Biology","url":"https://www.academia.edu/Documents/in/Plant_Biology?f_ri=3243133","nofollow":false},{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology?f_ri=3243133","nofollow":false},{"id":13827,"name":"Cell 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href="https://www.academia.edu/39814296/Large_Scale_Culture_of_Ginseng_Adventitious_Roots_for_Production_of_Ginsenosides">Large Scale Culture of Ginseng Adventitious Roots for Production of Ginsenosides</a></div></div><div class="u-pb4x u-mt3x"></div><ul class="InlineList u-ph0x u-fs13"><li class="InlineList-item logged_in_only"><div class="share_on_academia_work_button"><a class="academia_share Button Button--inverseBlue Button--sm js-bookmark-button" data-academia-share="Work/39814296" data-share-source="work_strip" data-spinner="small_white_hide_contents"><i class="fa fa-plus"></i><span class="work-strip-link-text u-ml1x" data-content="button_text">Bookmark</span></a></div></li><li class="InlineList-item"><div class="download"><a id="57fe58704da392faad364bcf460355eb" rel="nofollow" data-download="{"attachment_id":59999881,"asset_id":39814296,"asset_type":"Work","always_allow_download":false,"track":null,"button_location":"work_strip","source":null,"hide_modal":null}" class="Button 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data-has-card-for-ri="66089" href="https://www.academia.edu/Documents/in/Tissue_culture">Tissue culture</a>, <script data-card-contents-for-ri="66089" type="text/json">{"id":66089,"name":"Tissue culture","url":"https://www.academia.edu/Documents/in/Tissue_culture?f_ri=3243133","nofollow":false}</script><a class="InlineList-item-text" data-has-card-for-ri="115090" href="https://www.academia.edu/Documents/in/Plant_Growth_Regulators">Plant Growth Regulators</a><script data-card-contents-for-ri="115090" type="text/json">{"id":115090,"name":"Plant Growth Regulators","url":"https://www.academia.edu/Documents/in/Plant_Growth_Regulators?f_ri=3243133","nofollow":false}</script></span></li><script>(function(){ if (true) { new Aedu.ResearchInterestListCard({ el: $('*[data-has-card-for-ri-list=39814296]'), work: {"id":39814296,"title":"Large Scale Culture of Ginseng Adventitious Roots for Production of 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class="clearfix u-pv7x u-mb0x js-work-card work_74533887" data-work_id="74533887" itemscope="itemscope" itemtype="https://schema.org/ScholarlyArticle"><div class="header"><div class="title u-fontSerif u-fs22 u-lineHeight1_3"><a class="u-tcGrayDarkest js-work-link" href="https://www.academia.edu/74533887/A_fungal_endophyte_helps_plants_to_tolerate_root_herbivory_through_changes_in_gibberellin_and_jasmonate_signaling">A fungal endophyte helps plants to tolerate root herbivory through changes in gibberellin and jasmonate signaling</a></div></div><div class="u-pb4x u-mt3x"><div class="summary u-fs14 u-fw300 u-lineHeight1_5 u-tcGrayDarkest"><div class="summarized">Plant-microbe mutualisms can improve plant defense, but the impact of root endophytes on below-ground herbivore interactions remains unknown. We investigated the effects of the root endophyte Piriformospora indica on interactions between... <a class="more_link u-tcGrayDark u-linkUnstyled" data-container=".work_74533887" data-show=".complete" data-hide=".summarized" data-more-link-behavior="true" href="#">more</a></div><div class="complete hidden">Plant-microbe mutualisms can improve plant defense, but the impact of root endophytes on below-ground herbivore interactions remains unknown. We investigated the effects of the root endophyte Piriformospora indica on interactions between rice (Oryza sativa) plants and its root herbivore rice water weevil (RWW; Lissorhoptrus oryzophilus), and how plant jasmonic acid (JA) and GA regulate this tripartite interaction. Glasshouse experiments with wild-type rice and coi1-18 and Eui1-OX mutants combined with nutrient, jasmonate and gene expression analyses were used to test: whether RWW adult herbivory above ground influences subsequent damage caused by larval herbivory below ground; whether P. indica protects plants against RWW; and whether GA and JA signaling mediate these interactions. The endophyte induced plant tolerance to root herbivory. RWW adults and larvae acted synergistically via JA signaling to reduce root growth, while endophyte-elicited GA biosynthesis suppressed the herbivo...</div></div></div><ul class="InlineList u-ph0x u-fs13"><li class="InlineList-item logged_in_only"><div class="share_on_academia_work_button"><a class="academia_share Button Button--inverseBlue Button--sm js-bookmark-button" data-academia-share="Work/74533887" data-share-source="work_strip" data-spinner="small_white_hide_contents"><i class="fa fa-plus"></i><span class="work-strip-link-text u-ml1x" data-content="button_text">Bookmark</span></a></div></li><li class="InlineList-item"><div class="download"><a id="8e04dfe2d2fcb2e13df6a27e9e3aa3ce" rel="nofollow" data-download="{"attachment_id":82651785,"asset_id":74533887,"asset_type":"Work","always_allow_download":false,"track":null,"button_location":"work_strip","source":null,"hide_modal":null}" class="Button Button--sm Button--inverseGreen js-download-button prompt_button doc_download" href="https://www.academia.edu/attachments/82651785/download_file?st=MTczMjQ1MjUxNyw4LjIyMi4yMDguMTQ2&s=work_strip"><i class="fa fa-arrow-circle-o-down fa-lg"></i><span class="u-textUppercase u-ml1x" data-content="button_text">Download</span></a></div></li><li class="InlineList-item"><ul class="InlineList InlineList--bordered u-ph0x"><li class="InlineList-item InlineList-item--bordered"><span class="InlineList-item-text">by <span itemscope="itemscope" itemprop="author" itemtype="https://schema.org/Person"><a class="u-tcGrayDark u-fw700" data-has-card-for-user="50177525" href="https://independent.academia.edu/MichaelStout1">Michael Stout</a><script data-card-contents-for-user="50177525" type="text/json">{"id":50177525,"first_name":"Michael","last_name":"Stout","domain_name":"independent","page_name":"MichaelStout1","display_name":"Michael Stout","profile_url":"https://independent.academia.edu/MichaelStout1?f_ri=3243133","photo":"/images/s65_no_pic.png"}</script></span></span></li><li class="js-paper-rank-work_74533887 InlineList-item InlineList-item--bordered hidden"><span class="js-paper-rank-view hidden u-tcGrayDark" data-paper-rank-work-id="74533887"><i class="u-m1x fa fa-bar-chart"></i><strong class="js-paper-rank"></strong></span><script>$(function() { new Works.PaperRankView({ workId: 74533887, container: ".js-paper-rank-work_74533887", }); 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We investigated the effects of the root endophyte Piriformospora indica on interactions between rice (Oryza sativa) plants and its root herbivore rice water weevil (RWW; Lissorhoptrus oryzophilus), and how plant jasmonic acid (JA) and GA regulate this tripartite interaction. Glasshouse experiments with wild-type rice and coi1-18 and Eui1-OX mutants combined with nutrient, jasmonate and gene expression analyses were used to test: whether RWW adult herbivory above ground influences subsequent damage caused by larval herbivory below ground; whether P. indica protects plants against RWW; and whether GA and JA signaling mediate these interactions. The endophyte induced plant tolerance to root herbivory. RWW adults and larvae acted synergistically via JA signaling to reduce root growth, while endophyte-elicited GA biosynthesis suppressed the herbivo...","downloadable_attachments":[{"id":82651785,"asset_id":74533887,"asset_type":"Work","always_allow_download":false}],"ordered_authors":[{"id":50177525,"first_name":"Michael","last_name":"Stout","domain_name":"independent","page_name":"MichaelStout1","display_name":"Michael Stout","profile_url":"https://independent.academia.edu/MichaelStout1?f_ri=3243133","photo":"/images/s65_no_pic.png"}],"research_interests":[{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology?f_ri=3243133","nofollow":false},{"id":26327,"name":"Medicine","url":"https://www.academia.edu/Documents/in/Medicine?f_ri=3243133","nofollow":false},{"id":38831,"name":"Signal Transduction","url":"https://www.academia.edu/Documents/in/Signal_Transduction?f_ri=3243133","nofollow":false},{"id":47884,"name":"Biological Sciences","url":"https://www.academia.edu/Documents/in/Biological_Sciences?f_ri=3243133","nofollow":false},{"id":66973,"name":"Plant diseases","url":"https://www.academia.edu/Documents/in/Plant_diseases?f_ri=3243133"},{"id":99234,"name":"Animals","url":"https://www.academia.edu/Documents/in/Animals?f_ri=3243133"},{"id":105062,"name":"Disease resistance","url":"https://www.academia.edu/Documents/in/Disease_resistance?f_ri=3243133"},{"id":141838,"name":"Herbivory","url":"https://www.academia.edu/Documents/in/Herbivory?f_ri=3243133"},{"id":143898,"name":"Endophytes","url":"https://www.academia.edu/Documents/in/Endophytes?f_ri=3243133"},{"id":192985,"name":"Weevils","url":"https://www.academia.edu/Documents/in/Weevils?f_ri=3243133"},{"id":202399,"name":"Plant Roots","url":"https://www.academia.edu/Documents/in/Plant_Roots?f_ri=3243133"},{"id":442493,"name":"Larva","url":"https://www.academia.edu/Documents/in/Larva?f_ri=3243133"},{"id":630848,"name":"Plant Development","url":"https://www.academia.edu/Documents/in/Plant_Development?f_ri=3243133"},{"id":1156097,"name":"Gibberellins","url":"https://www.academia.edu/Documents/in/Gibberellins?f_ri=3243133"},{"id":1746898,"name":"BASIDIOMYCOTA","url":"https://www.academia.edu/Documents/in/BASIDIOMYCOTA?f_ri=3243133"},{"id":3243133,"name":"Oxylipins","url":"https://www.academia.edu/Documents/in/Oxylipins?f_ri=3243133"}]}, }) } })();</script></ul></li></ul></div></div><div class="u-borderBottom1 u-borderColorGrayLighter"><div class="clearfix u-pv7x u-mb0x js-work-card work_71849665" data-work_id="71849665" itemscope="itemscope" itemtype="https://schema.org/ScholarlyArticle"><div class="header"><div class="title u-fontSerif u-fs22 u-lineHeight1_3"><a class="u-tcGrayDarkest js-work-link" href="https://www.academia.edu/71849665/Exogenous_Methyl_Jasmonate_and_Salicylic_Acid_Induce_Subspecies_Specific_Patterns_of_Glucosinolate_Accumulation_and_Gene_Expression_in_Brassica_oleracea_L">Exogenous Methyl Jasmonate and Salicylic Acid Induce Subspecies-Specific Patterns of Glucosinolate Accumulation and Gene Expression in Brassica oleracea L</a></div></div><div class="u-pb4x u-mt3x"><div class="summary u-fs14 u-fw300 u-lineHeight1_5 u-tcGrayDarkest"><div class="summarized">Glucosinolates have anti-carcinogenic properties. In the recent decades, the genetics of glucosinolate biosynthesis has been widely studied, however, the expression of specific genes involved in glucosinolate biosynthesis under exogenous... <a class="more_link u-tcGrayDark u-linkUnstyled" data-container=".work_71849665" data-show=".complete" data-hide=".summarized" data-more-link-behavior="true" href="#">more</a></div><div class="complete hidden">Glucosinolates have anti-carcinogenic properties. In the recent decades, the genetics of glucosinolate biosynthesis has been widely studied, however, the expression of specific genes involved in glucosinolate biosynthesis under exogenous phytohormone treatment has not been explored at the subspecies level in Brassica oleracea. Such data are vital for strategies aimed at selective exploitation of glucosinolate profiles. This study quantified the expression of 38 glucosinolate biosynthesis-related genes in three B. oleracea subspecies, namely cabbage, broccoli and kale, and catalogued associations between gene expression and increased contents of individual glucosinolates under methyl jasmonate (MeJA) and salicylic acid (SA) treatments. Glucosinolate accumulation and gene expression in response to phytohormone elicitation was subspecies specific. For instance, cabbage leaves showed enhanced accumulation of the aliphatic glucoiberin, progoitrin, sinigrin and indolic neoglucobrassicin u...</div></div></div><ul class="InlineList u-ph0x u-fs13"><li class="InlineList-item logged_in_only"><div class="share_on_academia_work_button"><a class="academia_share Button Button--inverseBlue Button--sm js-bookmark-button" data-academia-share="Work/71849665" data-share-source="work_strip" data-spinner="small_white_hide_contents"><i class="fa fa-plus"></i><span class="work-strip-link-text u-ml1x" data-content="button_text">Bookmark</span></a></div></li><li class="InlineList-item"><div class="download"><a id="e4a5203e027af4ed340c0986fcda241b" rel="nofollow" data-download="{"attachment_id":81028390,"asset_id":71849665,"asset_type":"Work","always_allow_download":false,"track":null,"button_location":"work_strip","source":null,"hide_modal":null}" class="Button Button--sm Button--inverseGreen js-download-button prompt_button doc_download" href="https://www.academia.edu/attachments/81028390/download_file?st=MTczMjQ1MjUxNyw4LjIyMi4yMDguMTQ2&s=work_strip"><i class="fa fa-arrow-circle-o-down fa-lg"></i><span class="u-textUppercase u-ml1x" data-content="button_text">Download</span></a></div></li><li class="InlineList-item"><ul class="InlineList InlineList--bordered u-ph0x"><li class="InlineList-item InlineList-item--bordered"><span class="InlineList-item-text">by <span itemscope="itemscope" itemprop="author" itemtype="https://schema.org/Person"><a class="u-tcGrayDark u-fw700" data-has-card-for-user="209299142" href="https://independent.academia.edu/DrArifHasanKhanRobin">Dr. Arif Hasan Khan Robin</a><script data-card-contents-for-user="209299142" type="text/json">{"id":209299142,"first_name":"Dr. Arif Hasan","last_name":"Khan Robin","domain_name":"independent","page_name":"DrArifHasanKhanRobin","display_name":"Dr. Arif Hasan Khan Robin","profile_url":"https://independent.academia.edu/DrArifHasanKhanRobin?f_ri=3243133","photo":"https://0.academia-photos.com/209299142/69143027/57537243/s65_dr._arif_hasan.khan_robin.jpeg"}</script></span></span></li><li class="js-paper-rank-work_71849665 InlineList-item InlineList-item--bordered hidden"><span class="js-paper-rank-view hidden u-tcGrayDark" data-paper-rank-work-id="71849665"><i class="u-m1x fa fa-bar-chart"></i><strong class="js-paper-rank"></strong></span><script>$(function() { new Works.PaperRankView({ workId: 71849665, container: ".js-paper-rank-work_71849665", }); 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In the recent decades, the genetics of glucosinolate biosynthesis has been widely studied, however, the expression of specific genes involved in glucosinolate biosynthesis under exogenous phytohormone treatment has not been explored at the subspecies level in Brassica oleracea. Such data are vital for strategies aimed at selective exploitation of glucosinolate profiles. This study quantified the expression of 38 glucosinolate biosynthesis-related genes in three B. oleracea subspecies, namely cabbage, broccoli and kale, and catalogued associations between gene expression and increased contents of individual glucosinolates under methyl jasmonate (MeJA) and salicylic acid (SA) treatments. Glucosinolate accumulation and gene expression in response to phytohormone elicitation was subspecies specific. For instance, cabbage leaves showed enhanced accumulation of the aliphatic glucoiberin, progoitrin, sinigrin and indolic neoglucobrassicin u...","downloadable_attachments":[{"id":81028390,"asset_id":71849665,"asset_type":"Work","always_allow_download":false}],"ordered_authors":[{"id":209299142,"first_name":"Dr. Arif Hasan","last_name":"Khan Robin","domain_name":"independent","page_name":"DrArifHasanKhanRobin","display_name":"Dr. Arif Hasan Khan Robin","profile_url":"https://independent.academia.edu/DrArifHasanKhanRobin?f_ri=3243133","photo":"https://0.academia-photos.com/209299142/69143027/57537243/s65_dr._arif_hasan.khan_robin.jpeg"}],"research_interests":[{"id":531,"name":"Organic Chemistry","url":"https://www.academia.edu/Documents/in/Organic_Chemistry?f_ri=3243133","nofollow":false},{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology?f_ri=3243133","nofollow":false},{"id":26327,"name":"Medicine","url":"https://www.academia.edu/Documents/in/Medicine?f_ri=3243133","nofollow":false},{"id":328449,"name":"Molecules","url":"https://www.academia.edu/Documents/in/Molecules?f_ri=3243133","nofollow":false},{"id":376268,"name":"Brassica","url":"https://www.academia.edu/Documents/in/Brassica?f_ri=3243133"},{"id":835980,"name":"Glucosinolates","url":"https://www.academia.edu/Documents/in/Glucosinolates?f_ri=3243133"},{"id":1133885,"name":"Salicylic Acid","url":"https://www.academia.edu/Documents/in/Salicylic_Acid?f_ri=3243133"},{"id":3243133,"name":"Oxylipins","url":"https://www.academia.edu/Documents/in/Oxylipins?f_ri=3243133"}]}, }) } })();</script></ul></li></ul></div></div><div class="u-borderBottom1 u-borderColorGrayLighter"><div 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jasmonic acid</a></div></div><div class="u-pb4x u-mt3x"></div><ul class="InlineList u-ph0x u-fs13"><li class="InlineList-item logged_in_only"><div class="share_on_academia_work_button"><a class="academia_share Button Button--inverseBlue Button--sm js-bookmark-button" data-academia-share="Work/52409913" data-share-source="work_strip" data-spinner="small_white_hide_contents"><i class="fa fa-plus"></i><span class="work-strip-link-text u-ml1x" data-content="button_text">Bookmark</span></a></div></li><li class="InlineList-item"><div class="download"><a id="ecf040d7ac84bdc5bcfaac7d07ab09cb" rel="nofollow" data-download="{"attachment_id":69685931,"asset_id":52409913,"asset_type":"Work","always_allow_download":false,"track":null,"button_location":"work_strip","source":null,"hide_modal":null}" class="Button Button--sm Button--inverseGreen js-download-button prompt_button doc_download" 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acid","created_at":"2021-09-15T01:39:39.534-07:00","url":"https://www.academia.edu/52409913/The_sesquiterpene_botrydial_produced_by_Botrytis_cinerea_induces_the_hypersensitive_response_and_its_toxicity_is_modulated_by_host_signaling_pathways_mediated_by_salicylic_acid_and_jasmonic_acid?f_ri=3243133","dom_id":"work_52409913","summary":null,"downloadable_attachments":[{"id":69685931,"asset_id":52409913,"asset_type":"Work","always_allow_download":false}],"ordered_authors":[{"id":146180076,"first_name":"Isidro","last_name":"Gonzalez Collado","domain_name":"independent","page_name":"IsidroGonzalezCollado","display_name":"Isidro Gonzalez Collado","profile_url":"https://independent.academia.edu/IsidroGonzalezCollado?f_ri=3243133","photo":"/images/s65_no_pic.png"}],"research_interests":[{"id":156,"name":"Genetics","url":"https://www.academia.edu/Documents/in/Genetics?f_ri=3243133","nofollow":false},{"id":159,"name":"Microbiology","url":"https://www.academia.edu/Documents/in/Microbiology?f_ri=3243133","nofollow":false},{"id":5541,"name":"Plant Biology","url":"https://www.academia.edu/Documents/in/Plant_Biology?f_ri=3243133","nofollow":false},{"id":9109,"name":"Tobacco","url":"https://www.academia.edu/Documents/in/Tobacco?f_ri=3243133","nofollow":false},{"id":25657,"name":"Plant Molecular Biology","url":"https://www.academia.edu/Documents/in/Plant_Molecular_Biology?f_ri=3243133"},{"id":38831,"name":"Signal Transduction","url":"https://www.academia.edu/Documents/in/Signal_Transduction?f_ri=3243133"},{"id":66973,"name":"Plant diseases","url":"https://www.academia.edu/Documents/in/Plant_diseases?f_ri=3243133"},{"id":73619,"name":"Botrytis","url":"https://www.academia.edu/Documents/in/Botrytis?f_ri=3243133"},{"id":106562,"name":"Plant","url":"https://www.academia.edu/Documents/in/Plant?f_ri=3243133"},{"id":198630,"name":"Molecular Plant Microbe Interactions","url":"https://www.academia.edu/Documents/in/Molecular_Plant_Microbe_Interactions?f_ri=3243133"},{"id":202413,"name":"Arabidopsis","url":"https://www.academia.edu/Documents/in/Arabidopsis?f_ri=3243133"},{"id":239046,"name":"Sesquiterpenes","url":"https://www.academia.edu/Documents/in/Sesquiterpenes?f_ri=3243133"},{"id":1133885,"name":"Salicylic Acid","url":"https://www.academia.edu/Documents/in/Salicylic_Acid?f_ri=3243133"},{"id":1905343,"name":"Plant Leaves","url":"https://www.academia.edu/Documents/in/Plant_Leaves?f_ri=3243133"},{"id":2230327,"name":"Aldehydes","url":"https://www.academia.edu/Documents/in/Aldehydes?f_ri=3243133"},{"id":2281154,"name":"Terpenoid","url":"https://www.academia.edu/Documents/in/Terpenoid?f_ri=3243133"},{"id":3243133,"name":"Oxylipins","url":"https://www.academia.edu/Documents/in/Oxylipins?f_ri=3243133"}]}, }) } })();</script></ul></li></ul></div></div><div class="u-borderBottom1 u-borderColorGrayLighter"><div class="clearfix u-pv7x u-mb0x js-work-card work_75435221" data-work_id="75435221" itemscope="itemscope" itemtype="https://schema.org/ScholarlyArticle"><div class="header"><div class="title u-fontSerif u-fs22 u-lineHeight1_3"><a class="u-tcGrayDarkest js-work-link" href="https://www.academia.edu/75435221/Polyamine_Oxidase_5_loss_of_function_mutations_in_Arabidopsis_thaliana_trigger_metabolic_and_transcriptional_reprogramming_and_promote_salt_stress_tolerance">Polyamine Oxidase 5 loss-of-function mutations in Arabidopsis thaliana trigger metabolic and transcriptional reprogramming and promote salt stress tolerance</a></div></div><div class="u-pb4x u-mt3x"><div class="summary u-fs14 u-fw300 u-lineHeight1_5 u-tcGrayDarkest"><div class="summarized">The family of polyamine oxidases (PAO) in Arabidopsis (AtPAO1-5) mediates polyamine (PA) back-conversion, which reverses the PA biosynthetic pathway from spermine, and its structural isomer thermospermine (tSpm), into spermidine and then... <a class="more_link u-tcGrayDark u-linkUnstyled" data-container=".work_75435221" data-show=".complete" data-hide=".summarized" data-more-link-behavior="true" href="#">more</a></div><div class="complete hidden">The family of polyamine oxidases (PAO) in Arabidopsis (AtPAO1-5) mediates polyamine (PA) back-conversion, which reverses the PA biosynthetic pathway from spermine, and its structural isomer thermospermine (tSpm), into spermidine and then putrescine. Here, we have studied the involvement of PA back-conversion in Arabidopsis salinity tolerance. AtPAO5 is the Arabidopsis PAO gene member most transcriptionally induced by salt stress. Two independent loss-of-function mutants (atpao5-2 and atpao5-3) were found to exhibit constitutively higher tSpm levels, with associated increased salt tolerance. Using global transcriptional and metabolomic analyses, the underlying mechanisms were studied. Stimulation of abscisic acid and jasmonates (JA) biosynthesis, and accumulation of important compatible solutes, such as sugars, polyols and proline, as well as TCA cycle intermediates were observed in atpao5 mutants under salt stress. Expression analyses indicate that tSpm modulates the transcript leve...</div></div></div><ul class="InlineList u-ph0x u-fs13"><li class="InlineList-item logged_in_only"><div class="share_on_academia_work_button"><a class="academia_share Button Button--inverseBlue Button--sm js-bookmark-button" data-academia-share="Work/75435221" data-share-source="work_strip" data-spinner="small_white_hide_contents"><i class="fa fa-plus"></i><span class="work-strip-link-text u-ml1x" data-content="button_text">Bookmark</span></a></div></li><li class="InlineList-item"><div class="download"><a id="915a45721c76c0713c037582e6c14524" rel="nofollow" data-download="{"attachment_id":83205040,"asset_id":75435221,"asset_type":"Work","always_allow_download":false,"track":null,"button_location":"work_strip","source":null,"hide_modal":null}" class="Button Button--sm Button--inverseGreen js-download-button prompt_button doc_download" href="https://www.academia.edu/attachments/83205040/download_file?st=MTczMjQ1MjUxNyw4LjIyMi4yMDguMTQ2&s=work_strip"><i class="fa fa-arrow-circle-o-down fa-lg"></i><span class="u-textUppercase u-ml1x" data-content="button_text">Download</span></a></div></li><li class="InlineList-item"><ul class="InlineList InlineList--bordered u-ph0x"><li class="InlineList-item InlineList-item--bordered"><span class="InlineList-item-text">by <span itemscope="itemscope" itemprop="author" itemtype="https://schema.org/Person"><a class="u-tcGrayDark u-fw700" data-has-card-for-user="111200468" href="https://uva.academia.edu/TeunMunnik">Teun Munnik</a><script data-card-contents-for-user="111200468" type="text/json">{"id":111200468,"first_name":"Teun","last_name":"Munnik","domain_name":"uva","page_name":"TeunMunnik","display_name":"Teun Munnik","profile_url":"https://uva.academia.edu/TeunMunnik?f_ri=3243133","photo":"https://0.academia-photos.com/111200468/46788172/36048181/s65_teun.munnik.jpg"}</script></span></span></li><li class="js-paper-rank-work_75435221 InlineList-item InlineList-item--bordered hidden"><span class="js-paper-rank-view hidden u-tcGrayDark" data-paper-rank-work-id="75435221"><i class="u-m1x fa fa-bar-chart"></i><strong class="js-paper-rank"></strong></span><script>$(function() { new Works.PaperRankView({ workId: 75435221, container: ".js-paper-rank-work_75435221", }); 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$(".js-view-count[data-work-id=75435221]").text(description); $(".js-view-count-work_75435221").attr('title', description).tooltip(); }); });</script></span><script>$(function() { $(".js-view-count-work_75435221").removeClass('hidden') })</script></div></li><li class="InlineList-item u-positionRelative" style="max-width: 250px"><div class="u-positionAbsolute" data-has-card-for-ri-list="75435221"><i class="fa fa-tag InlineList-item-icon u-positionRelative"></i>  <a class="InlineList-item-text u-positionRelative">20</a>  </div><span class="InlineList-item-text u-textTruncate u-pl10x"><a class="InlineList-item-text" data-has-card-for-ri="5069" href="https://www.academia.edu/Documents/in/Principal_Component_Analysis">Principal Component Analysis</a>, <script data-card-contents-for-ri="5069" type="text/json">{"id":5069,"name":"Principal Component Analysis","url":"https://www.academia.edu/Documents/in/Principal_Component_Analysis?f_ri=3243133","nofollow":false}</script><a class="InlineList-item-text" data-has-card-for-ri="7710" href="https://www.academia.edu/Documents/in/Biology">Biology</a>, <script data-card-contents-for-ri="7710" type="text/json">{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology?f_ri=3243133","nofollow":false}</script><a class="InlineList-item-text" data-has-card-for-ri="26327" href="https://www.academia.edu/Documents/in/Medicine">Medicine</a>, <script data-card-contents-for-ri="26327" type="text/json">{"id":26327,"name":"Medicine","url":"https://www.academia.edu/Documents/in/Medicine?f_ri=3243133","nofollow":false}</script><a class="InlineList-item-text" data-has-card-for-ri="43761" href="https://www.academia.edu/Documents/in/Transcriptome">Transcriptome</a><script data-card-contents-for-ri="43761" type="text/json">{"id":43761,"name":"Transcriptome","url":"https://www.academia.edu/Documents/in/Transcriptome?f_ri=3243133","nofollow":false}</script></span></li><script>(function(){ if (true) { new Aedu.ResearchInterestListCard({ el: $('*[data-has-card-for-ri-list=75435221]'), work: {"id":75435221,"title":"Polyamine Oxidase 5 loss-of-function mutations in Arabidopsis thaliana trigger metabolic and transcriptional reprogramming and promote salt stress tolerance","created_at":"2022-04-04T08:27:07.153-07:00","url":"https://www.academia.edu/75435221/Polyamine_Oxidase_5_loss_of_function_mutations_in_Arabidopsis_thaliana_trigger_metabolic_and_transcriptional_reprogramming_and_promote_salt_stress_tolerance?f_ri=3243133","dom_id":"work_75435221","summary":"The family of polyamine oxidases (PAO) in Arabidopsis (AtPAO1-5) mediates polyamine (PA) back-conversion, which reverses the PA biosynthetic pathway from spermine, and its structural isomer thermospermine (tSpm), into spermidine and then putrescine. Here, we have studied the involvement of PA back-conversion in Arabidopsis salinity tolerance. AtPAO5 is the Arabidopsis PAO gene member most transcriptionally induced by salt stress. Two independent loss-of-function mutants (atpao5-2 and atpao5-3) were found to exhibit constitutively higher tSpm levels, with associated increased salt tolerance. Using global transcriptional and metabolomic analyses, the underlying mechanisms were studied. Stimulation of abscisic acid and jasmonates (JA) biosynthesis, and accumulation of important compatible solutes, such as sugars, polyols and proline, as well as TCA cycle intermediates were observed in atpao5 mutants under salt stress. Expression analyses indicate that tSpm modulates the transcript leve...","downloadable_attachments":[{"id":83205040,"asset_id":75435221,"asset_type":"Work","always_allow_download":false}],"ordered_authors":[{"id":111200468,"first_name":"Teun","last_name":"Munnik","domain_name":"uva","page_name":"TeunMunnik","display_name":"Teun Munnik","profile_url":"https://uva.academia.edu/TeunMunnik?f_ri=3243133","photo":"https://0.academia-photos.com/111200468/46788172/36048181/s65_teun.munnik.jpg"}],"research_interests":[{"id":5069,"name":"Principal Component Analysis","url":"https://www.academia.edu/Documents/in/Principal_Component_Analysis?f_ri=3243133","nofollow":false},{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology?f_ri=3243133","nofollow":false},{"id":26327,"name":"Medicine","url":"https://www.academia.edu/Documents/in/Medicine?f_ri=3243133","nofollow":false},{"id":43761,"name":"Transcriptome","url":"https://www.academia.edu/Documents/in/Transcriptome?f_ri=3243133","nofollow":false},{"id":47884,"name":"Biological Sciences","url":"https://www.academia.edu/Documents/in/Biological_Sciences?f_ri=3243133"},{"id":129210,"name":"Gene ontology","url":"https://www.academia.edu/Documents/in/Gene_ontology?f_ri=3243133"},{"id":202413,"name":"Arabidopsis","url":"https://www.academia.edu/Documents/in/Arabidopsis?f_ri=3243133"},{"id":212480,"name":"Abscisic Acid","url":"https://www.academia.edu/Documents/in/Abscisic_Acid?f_ri=3243133"},{"id":213897,"name":"Phenotype","url":"https://www.academia.edu/Documents/in/Phenotype?f_ri=3243133"},{"id":231390,"name":"SALT TOLERANCE","url":"https://www.academia.edu/Documents/in/SALT_TOLERANCE?f_ri=3243133"},{"id":274826,"name":"Hydrogen Peroxide","url":"https://www.academia.edu/Documents/in/Hydrogen_Peroxide?f_ri=3243133"},{"id":386342,"name":"Sodium","url":"https://www.academia.edu/Documents/in/Sodium?f_ri=3243133"},{"id":421781,"name":"Spermine","url":"https://www.academia.edu/Documents/in/Spermine?f_ri=3243133"},{"id":1223913,"name":"Sodium Chloride","url":"https://www.academia.edu/Documents/in/Sodium_Chloride?f_ri=3243133"},{"id":1257974,"name":"Ions","url":"https://www.academia.edu/Documents/in/Ions?f_ri=3243133"},{"id":1292327,"name":"Metabolome","url":"https://www.academia.edu/Documents/in/Metabolome?f_ri=3243133"},{"id":1537773,"name":"Loss of Function Mutation","url":"https://www.academia.edu/Documents/in/Loss_of_Function_Mutation?f_ri=3243133"},{"id":1810445,"name":"Gene expression profiling","url":"https://www.academia.edu/Documents/in/Gene_expression_profiling?f_ri=3243133"},{"id":3243133,"name":"Oxylipins","url":"https://www.academia.edu/Documents/in/Oxylipins?f_ri=3243133"},{"id":3647007,"name":"Stress Physiological","url":"https://www.academia.edu/Documents/in/Stress_Physiological?f_ri=3243133"}]}, }) } })();</script></ul></li></ul></div></div><div class="u-borderBottom1 u-borderColorGrayLighter"><div class="clearfix u-pv7x u-mb0x js-work-card work_75249843" data-work_id="75249843" itemscope="itemscope" itemtype="https://schema.org/ScholarlyArticle"><div class="header"><div class="title u-fontSerif u-fs22 u-lineHeight1_3"><a class="u-tcGrayDarkest js-work-link" href="https://www.academia.edu/75249843/Pseudomonas_syringae_Type_III_Effector_HopBB1_Promotes_Host_Transcriptional_Repressor_Degradation_to_Regulate_Phytohormone_Responses_and_Virulence">Pseudomonas syringae Type III Effector HopBB1 Promotes Host Transcriptional Repressor Degradation to Regulate Phytohormone Responses and Virulence</a></div></div><div class="u-pb4x u-mt3x"><div class="summary u-fs14 u-fw300 u-lineHeight1_5 u-tcGrayDarkest"><div class="summarized">Independently evolved pathogen effectors from three branches of life (ascomycete, eubacteria, and oomycete) converge onto the Arabidopsis TCP14 transcription factor to manipulate host defense. However, the mechanistic basis for defense... <a class="more_link u-tcGrayDark u-linkUnstyled" data-container=".work_75249843" data-show=".complete" data-hide=".summarized" data-more-link-behavior="true" href="#">more</a></div><div class="complete hidden">Independently evolved pathogen effectors from three branches of life (ascomycete, eubacteria, and oomycete) converge onto the Arabidopsis TCP14 transcription factor to manipulate host defense. However, the mechanistic basis for defense control via TCP14 regulation is unknown. We demonstrate that TCP14 regulates the plant immune system by transcriptionally repressing a subset of the jasmonic acid (JA) hormone signaling outputs. A previously unstudied Pseudomonas syringae (Psy) type III effector, HopBB1, interacts with TCP14 and targets it to the SCF(COI1) degradation complex by connecting it to the JA signaling repressor JAZ3. Consequently, HopBB1 de-represses the TCP14-regulated subset of JA response genes and promotes pathogen virulence. Thus, HopBB1 fine-tunes host phytohormone crosstalk by precisely manipulating part of the JA regulon to avoid pleiotropic host responses while promoting pathogen proliferation.</div></div></div><ul class="InlineList u-ph0x u-fs13"><li class="InlineList-item logged_in_only"><div class="share_on_academia_work_button"><a class="academia_share Button Button--inverseBlue Button--sm js-bookmark-button" data-academia-share="Work/75249843" data-share-source="work_strip" data-spinner="small_white_hide_contents"><i class="fa fa-plus"></i><span class="work-strip-link-text u-ml1x" data-content="button_text">Bookmark</span></a></div></li><li class="InlineList-item"><div class="download"><a id="86602d75b2562edd6ea6330fbe60da46" rel="nofollow" data-download="{"attachment_id":83094577,"asset_id":75249843,"asset_type":"Work","always_allow_download":false,"track":null,"button_location":"work_strip","source":null,"hide_modal":null}" class="Button Button--sm Button--inverseGreen js-download-button prompt_button doc_download" href="https://www.academia.edu/attachments/83094577/download_file?st=MTczMjQ1MjUxNyw4LjIyMi4yMDguMTQ2&s=work_strip"><i class="fa fa-arrow-circle-o-down fa-lg"></i><span class="u-textUppercase u-ml1x" data-content="button_text">Download</span></a></div></li><li class="InlineList-item"><ul class="InlineList InlineList--bordered u-ph0x"><li class="InlineList-item InlineList-item--bordered"><span class="InlineList-item-text">by <span itemscope="itemscope" itemprop="author" itemtype="https://schema.org/Person"><a class="u-tcGrayDark u-fw700" data-has-card-for-user="125084849" href="https://sunysuffolk.academia.edu/isaigonzalez">isai gonzalez</a><script data-card-contents-for-user="125084849" type="text/json">{"id":125084849,"first_name":"isai","last_name":"gonzalez","domain_name":"sunysuffolk","page_name":"isaigonzalez","display_name":"isai gonzalez","profile_url":"https://sunysuffolk.academia.edu/isaigonzalez?f_ri=3243133","photo":"https://0.academia-photos.com/125084849/47461702/36350012/s65_isai.gonzalez.jpg"}</script></span></span></li><li class="js-paper-rank-work_75249843 InlineList-item InlineList-item--bordered hidden"><span class="js-paper-rank-view hidden u-tcGrayDark" data-paper-rank-work-id="75249843"><i class="u-m1x fa fa-bar-chart"></i><strong class="js-paper-rank"></strong></span><script>$(function() { new Works.PaperRankView({ workId: 75249843, container: ".js-paper-rank-work_75249843", }); 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However, the mechanistic basis for defense control via TCP14 regulation is unknown. We demonstrate that TCP14 regulates the plant immune system by transcriptionally repressing a subset of the jasmonic acid (JA) hormone signaling outputs. A previously unstudied Pseudomonas syringae (Psy) type III effector, HopBB1, interacts with TCP14 and targets it to the SCF(COI1) degradation complex by connecting it to the JA signaling repressor JAZ3. Consequently, HopBB1 de-represses the TCP14-regulated subset of JA response genes and promotes pathogen virulence. Thus, HopBB1 fine-tunes host phytohormone crosstalk by precisely manipulating part of the JA regulon to avoid pleiotropic host responses while promoting pathogen proliferation.","downloadable_attachments":[{"id":83094577,"asset_id":75249843,"asset_type":"Work","always_allow_download":false}],"ordered_authors":[{"id":125084849,"first_name":"isai","last_name":"gonzalez","domain_name":"sunysuffolk","page_name":"isaigonzalez","display_name":"isai gonzalez","profile_url":"https://sunysuffolk.academia.edu/isaigonzalez?f_ri=3243133","photo":"https://0.academia-photos.com/125084849/47461702/36350012/s65_isai.gonzalez.jpg"}],"research_interests":[{"id":159,"name":"Microbiology","url":"https://www.academia.edu/Documents/in/Microbiology?f_ri=3243133","nofollow":false},{"id":6947,"name":"Medical Microbiology","url":"https://www.academia.edu/Documents/in/Medical_Microbiology?f_ri=3243133","nofollow":false},{"id":7710,"name":"Biology","url":"https://www.academia.edu/Documents/in/Biology?f_ri=3243133","nofollow":false},{"id":9109,"name":"Tobacco","url":"https://www.academia.edu/Documents/in/Tobacco?f_ri=3243133","nofollow":false},{"id":23323,"name":"Transcription Factors","url":"https://www.academia.edu/Documents/in/Transcription_Factors?f_ri=3243133"},{"id":26327,"name":"Medicine","url":"https://www.academia.edu/Documents/in/Medicine?f_ri=3243133"},{"id":38831,"name":"Signal Transduction","url":"https://www.academia.edu/Documents/in/Signal_Transduction?f_ri=3243133"},{"id":66973,"name":"Plant diseases","url":"https://www.academia.edu/Documents/in/Plant_diseases?f_ri=3243133"},{"id":115090,"name":"Plant Growth Regulators","url":"https://www.academia.edu/Documents/in/Plant_Growth_Regulators?f_ri=3243133"},{"id":202413,"name":"Arabidopsis","url":"https://www.academia.edu/Documents/in/Arabidopsis?f_ri=3243133"},{"id":277229,"name":"Pseudomonas Syringae","url":"https://www.academia.edu/Documents/in/Pseudomonas_Syringae?f_ri=3243133"},{"id":743643,"name":"Host Pathogen Interactions","url":"https://www.academia.edu/Documents/in/Host_Pathogen_Interactions?f_ri=3243133"},{"id":783233,"name":"Plant immunity","url":"https://www.academia.edu/Documents/in/Plant_immunity?f_ri=3243133"},{"id":3243133,"name":"Oxylipins","url":"https://www.academia.edu/Documents/in/Oxylipins?f_ri=3243133"}]}, }) } })();</script></ul></li></ul></div></div><div class="u-borderBottom1 u-borderColorGrayLighter"><div class="clearfix u-pv7x u-mb0x js-work-card work_70911623" data-work_id="70911623" itemscope="itemscope" itemtype="https://schema.org/ScholarlyArticle"><div class="header"><div class="title u-fontSerif u-fs22 u-lineHeight1_3"><a class="u-tcGrayDarkest js-work-link" href="https://www.academia.edu/70911623/Elicitorinduced_defense_responses_in_Solanum_lycopersium_against_Ralstonia_solanacearum_The_Scientific">Elicitorinduced defense responses in Solanum lycopersium against Ralstonia solanacearum,”The Scientific</a></div></div><div class="u-pb4x u-mt3x"><div class="summary u-fs14 u-fw300 u-lineHeight1_5 u-tcGrayDarkest"><div class="summarized">We investigated on important parameters of induced resistance in hydroponic tomato (Solanum lycopersicum) against Ralstonia solanacearum using the elicitors chitosan (CHT), salicylic acid (SA), and jasmonic acid (JA). The increase in... <a class="more_link u-tcGrayDark u-linkUnstyled" data-container=".work_70911623" data-show=".complete" data-hide=".summarized" data-more-link-behavior="true" href="#">more</a></div><div class="complete hidden">We investigated on important parameters of induced resistance in hydroponic tomato (Solanum lycopersicum) against Ralstonia solanacearum using the elicitors chitosan (CHT), salicylic acid (SA), and jasmonic acid (JA). The increase in total phenolic content of roots by the elicitors was significantly higher than control. Most pronounced increase in lignin synthesis was triggered by SA followed by CHT. At 24 h post-elicitation (hpe), the activity of phenylalanine ammonia lyase was 4.5 times higher than control elicited by CHT. The peroxidase activity was about 86 nkat/mg protein at 24 hpe in case of SA and 78 nkat/mg protein in case of CHT. The activity of polyphenol oxidase increased several folds by the elicitors. Cinnamyl alcohol dehydrogenase activity increased to the maximum at 48 hpe under the influence of CHT. The results indicate that the elicitors SA and CHT induced effective defense responses in tomato plants against R. solanacearum. This was evident from reduced vascular br...</div></div></div><ul class="InlineList u-ph0x u-fs13"><li class="InlineList-item logged_in_only"><div class="share_on_academia_work_button"><a class="academia_share Button Button--inverseBlue Button--sm js-bookmark-button" data-academia-share="Work/70911623" data-share-source="work_strip" data-spinner="small_white_hide_contents"><i class="fa fa-plus"></i><span class="work-strip-link-text u-ml1x" data-content="button_text">Bookmark</span></a></div></li><li class="InlineList-item"><div class="download"><a id="7b645af4e0516af87ce7cc86d76ae1c4" rel="nofollow" data-download="{"attachment_id":80465125,"asset_id":70911623,"asset_type":"Work","always_allow_download":false,"track":null,"button_location":"work_strip","source":null,"hide_modal":null}" class="Button Button--sm Button--inverseGreen js-download-button prompt_button doc_download" href="https://www.academia.edu/attachments/80465125/download_file?st=MTczMjQ1MjUxNyw4LjIyMi4yMDguMTQ2&s=work_strip"><i class="fa fa-arrow-circle-o-down fa-lg"></i><span class="u-textUppercase u-ml1x" data-content="button_text">Download</span></a></div></li><li class="InlineList-item"><ul class="InlineList InlineList--bordered u-ph0x"><li class="InlineList-item InlineList-item--bordered"><span class="InlineList-item-text">by <span itemscope="itemscope" itemprop="author" itemtype="https://schema.org/Person"><a class="u-tcGrayDark u-fw700" data-has-card-for-user="22197616" href="https://independent.academia.edu/itishreekar">itishree kar</a><script data-card-contents-for-user="22197616" type="text/json">{"id":22197616,"first_name":"itishree","last_name":"kar","domain_name":"independent","page_name":"itishreekar","display_name":"itishree kar","profile_url":"https://independent.academia.edu/itishreekar?f_ri=3243133","photo":"https://0.academia-photos.com/22197616/6072163/6886389/s65_itishree.kar.jpg"}</script></span></span></li><li class="js-paper-rank-work_70911623 InlineList-item InlineList-item--bordered hidden"><span class="js-paper-rank-view hidden u-tcGrayDark" data-paper-rank-work-id="70911623"><i class="u-m1x fa fa-bar-chart"></i><strong class="js-paper-rank"></strong></span><script>$(function() { new Works.PaperRankView({ workId: 70911623, container: ".js-paper-rank-work_70911623", }); 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The increase in total phenolic content of roots by the elicitors was significantly higher than control. Most pronounced increase in lignin synthesis was triggered by SA followed by CHT. At 24 h post-elicitation (hpe), the activity of phenylalanine ammonia lyase was 4.5 times higher than control elicited by CHT. The peroxidase activity was about 86 nkat/mg protein at 24 hpe in case of SA and 78 nkat/mg protein in case of CHT. The activity of polyphenol oxidase increased several folds by the elicitors. Cinnamyl alcohol dehydrogenase activity increased to the maximum at 48 hpe under the influence of CHT. The results indicate that the elicitors SA and CHT induced effective defense responses in tomato plants against R. solanacearum. This was evident from reduced vascular br...","downloadable_attachments":[{"id":80465125,"asset_id":70911623,"asset_type":"Work","always_allow_download":false}],"ordered_authors":[{"id":22197616,"first_name":"itishree","last_name":"kar","domain_name":"independent","page_name":"itishreekar","display_name":"itishree kar","profile_url":"https://independent.academia.edu/itishreekar?f_ri=3243133","photo":"https://0.academia-photos.com/22197616/6072163/6886389/s65_itishree.kar.jpg"}],"research_interests":[{"id":7019,"name":"Hydroponics","url":"https://www.academia.edu/Documents/in/Hydroponics?f_ri=3243133","nofollow":false},{"id":9130,"name":"Chitosan","url":"https://www.academia.edu/Documents/in/Chitosan?f_ri=3243133","nofollow":false},{"id":66973,"name":"Plant diseases","url":"https://www.academia.edu/Documents/in/Plant_diseases?f_ri=3243133","nofollow":false},{"id":139007,"name":"Catalase","url":"https://www.academia.edu/Documents/in/Catalase?f_ri=3243133","nofollow":false},{"id":173023,"name":"Lignin","url":"https://www.academia.edu/Documents/in/Lignin?f_ri=3243133"},{"id":202399,"name":"Plant Roots","url":"https://www.academia.edu/Documents/in/Plant_Roots?f_ri=3243133"},{"id":347988,"name":"Phenols","url":"https://www.academia.edu/Documents/in/Phenols?f_ri=3243133"},{"id":413115,"name":"Peroxidases","url":"https://www.academia.edu/Documents/in/Peroxidases?f_ri=3243133"},{"id":743643,"name":"Host Pathogen Interactions","url":"https://www.academia.edu/Documents/in/Host_Pathogen_Interactions?f_ri=3243133"},{"id":1133885,"name":"Salicylic Acid","url":"https://www.academia.edu/Documents/in/Salicylic_Acid?f_ri=3243133"},{"id":1493934,"name":"Phenylalanine ammonia lyase","url":"https://www.academia.edu/Documents/in/Phenylalanine_ammonia_lyase?f_ri=3243133"},{"id":1640340,"name":"Lycopersicon esculentum","url":"https://www.academia.edu/Documents/in/Lycopersicon_esculentum?f_ri=3243133"},{"id":2081036,"name":"Ralstonia solanacearum","url":"https://www.academia.edu/Documents/in/Ralstonia_solanacearum?f_ri=3243133"},{"id":3243133,"name":"Oxylipins","url":"https://www.academia.edu/Documents/in/Oxylipins?f_ri=3243133"}]}, }) } })();</script></ul></li></ul></div></div><div class="u-borderBottom1 u-borderColorGrayLighter"><div class="clearfix u-pv7x u-mb0x js-work-card work_52330290" data-work_id="52330290" itemscope="itemscope" itemtype="https://schema.org/ScholarlyArticle"><div class="header"><div class="title u-fontSerif u-fs22 u-lineHeight1_3"><a class="u-tcGrayDarkest js-work-link" href="https://www.academia.edu/52330290/The_Role_of_Ethylene_and_Wound_Signaling_in_Resistance_of_Tomato_to_Botrytis_cinerea">The Role of Ethylene and Wound Signaling in 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href="https://www.academia.edu/52258135/Infection_of_Arabidopsis_with_a_necrotrophic_pathogen_Botrytis_cinerea_elicits_various_defense_responses_but_does_not_induce_systemic_acquired_resistance_SAR_">Infection of Arabidopsis with a necrotrophic pathogen, Botrytis cinerea, elicits various defense responses but does not induce systemic acquired resistance (SAR)</a></div></div><div class="u-pb4x u-mt3x"><div class="summary u-fs14 u-fw300 u-lineHeight1_5 u-tcGrayDarkest"><div class="summarized">Botrytis cinerea is a non-specific necrotrophic pathogen that attacks more than 200 plant species. In contrast to biotrophs, the necrotrophs obtain their nutrients by first killing the host cells. Many studies have shown that infection of... <a class="more_link u-tcGrayDark u-linkUnstyled" data-container=".work_52258135" data-show=".complete" data-hide=".summarized" data-more-link-behavior="true" href="#">more</a></div><div class="complete hidden">Botrytis cinerea is a non-specific necrotrophic pathogen that attacks more than 200 plant species. In contrast to biotrophs, the necrotrophs obtain their nutrients by first killing the host cells. Many studies have shown that infection of plants by necrosis-causing pathogens induces a systemic acquired resistance (SAR), which provides protection against successive infections by a range of pathogenic organisms. We analyzed the role of SAR in B. cinerea infection of Arabidopsis. We show that although B. cinerea induced necrotic lesions and camalexin biosynthesis, it did not induce SAR-mediated protection against virulent strains of Pseudomonas syringae, or against subsequent B. cinerea infections. Induction of SAR with avirulent P. syringae or by chemical treatment with salicylic acid (SA) or benzothiadiazole also failed to inhibit B. cinerea growth, although removal of basal SA accumulation by expression of a bacterial salicylate hydroxylase (NahG) gene or by infiltration of 2-aminoi...</div></div></div><ul class="InlineList u-ph0x u-fs13"><li class="InlineList-item logged_in_only"><div class="share_on_academia_work_button"><a class="academia_share Button Button--inverseBlue Button--sm js-bookmark-button" data-academia-share="Work/52258135" data-share-source="work_strip" data-spinner="small_white_hide_contents"><i class="fa fa-plus"></i><span class="work-strip-link-text u-ml1x" data-content="button_text">Bookmark</span></a></div></li><li class="InlineList-item"><div class="download"><a id="a29d1974f53bc6b9adf2b0528a663819" rel="nofollow" data-download="{"attachment_id":69607187,"asset_id":52258135,"asset_type":"Work","always_allow_download":false,"track":null,"button_location":"work_strip","source":null,"hide_modal":null}" class="Button Button--sm Button--inverseGreen js-download-button prompt_button doc_download" href="https://www.academia.edu/attachments/69607187/download_file?st=MTczMjQ1MjUxNyw4LjIyMi4yMDguMTQ2&s=work_strip"><i class="fa fa-arrow-circle-o-down fa-lg"></i><span class="u-textUppercase u-ml1x" data-content="button_text">Download</span></a></div></li><li class="InlineList-item"><ul class="InlineList InlineList--bordered u-ph0x"><li class="InlineList-item InlineList-item--bordered"><span class="InlineList-item-text">by <span itemscope="itemscope" itemprop="author" itemtype="https://schema.org/Person"><a class="u-tcGrayDark u-fw700" data-has-card-for-user="109164695" href="https://independent.academia.edu/AlexLevine13">Alex Levine</a><script data-card-contents-for-user="109164695" type="text/json">{"id":109164695,"first_name":"Alex","last_name":"Levine","domain_name":"independent","page_name":"AlexLevine13","display_name":"Alex Levine","profile_url":"https://independent.academia.edu/AlexLevine13?f_ri=3243133","photo":"/images/s65_no_pic.png"}</script></span></span></li><li class="js-paper-rank-work_52258135 InlineList-item InlineList-item--bordered hidden"><span class="js-paper-rank-view hidden u-tcGrayDark" data-paper-rank-work-id="52258135"><i class="u-m1x fa fa-bar-chart"></i><strong class="js-paper-rank"></strong></span><script>$(function() { new Works.PaperRankView({ workId: 52258135, container: ".js-paper-rank-work_52258135", }); 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In contrast to biotrophs, the necrotrophs obtain their nutrients by first killing the host cells. Many studies have shown that infection of plants by necrosis-causing pathogens induces a systemic acquired resistance (SAR), which provides protection against successive infections by a range of pathogenic organisms. We analyzed the role of SAR in B. cinerea infection of Arabidopsis. We show that although B. cinerea induced necrotic lesions and camalexin biosynthesis, it did not induce SAR-mediated protection against virulent strains of Pseudomonas syringae, or against subsequent B. cinerea infections. Induction of SAR with avirulent P. syringae or by chemical treatment with salicylic acid (SA) or benzothiadiazole also failed to inhibit B. cinerea growth, although removal of basal SA accumulation by expression of a bacterial salicylate hydroxylase (NahG) gene or by infiltration of 2-aminoi...","downloadable_attachments":[{"id":69607187,"asset_id":52258135,"asset_type":"Work","always_allow_download":false}],"ordered_authors":[{"id":109164695,"first_name":"Alex","last_name":"Levine","domain_name":"independent","page_name":"AlexLevine13","display_name":"Alex Levine","profile_url":"https://independent.academia.edu/AlexLevine13?f_ri=3243133","photo":"/images/s65_no_pic.png"}],"research_interests":[{"id":156,"name":"Genetics","url":"https://www.academia.edu/Documents/in/Genetics?f_ri=3243133","nofollow":false},{"id":5541,"name":"Plant Biology","url":"https://www.academia.edu/Documents/in/Plant_Biology?f_ri=3243133","nofollow":false},{"id":25657,"name":"Plant Molecular 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})();</script></ul></li></ul></div></div><div class="u-borderBottom1 u-borderColorGrayLighter"><div class="clearfix u-pv7x u-mb0x js-work-card work_74533875" data-work_id="74533875" itemscope="itemscope" itemtype="https://schema.org/ScholarlyArticle"><div class="header"><div class="title u-fontSerif u-fs22 u-lineHeight1_3"><a class="u-tcGrayDarkest js-work-link" href="https://www.academia.edu/74533875/Induced_jasmonate_signaling_leads_to_contrasting_effects_on_root_damage_and_herbivore_performance">Induced jasmonate signaling leads to contrasting effects on root damage and herbivore performance</a></div></div><div class="u-pb4x u-mt3x"><div class="summary u-fs14 u-fw300 u-lineHeight1_5 u-tcGrayDarkest"><div class="summarized">Induced defenses play a key role in plant resistance against leaf feeders. However, very little is known about the signals that are involved in defending plants against root feeders and how they are influenced by abiotic factors. We... <a class="more_link u-tcGrayDark u-linkUnstyled" data-container=".work_74533875" data-show=".complete" data-hide=".summarized" data-more-link-behavior="true" href="#">more</a></div><div class="complete hidden">Induced defenses play a key role in plant resistance against leaf feeders. However, very little is known about the signals that are involved in defending plants against root feeders and how they are influenced by abiotic factors. We investigated these aspects for the interaction between rice (Oryza sativa) and two root-feeding insects: the generalist cucumber beetle (Diabrotica balteata) and the more specialized rice water weevil (Lissorhoptrus oryzophilus). Rice plants responded to root attack by increasing the production of jasmonic acid (JA) and abscisic acid, whereas in contrast to in herbivore-attacked leaves, salicylic acid and ethylene levels remained unchanged. The JA response was decoupled from flooding and remained constant over different soil moisture levels. Exogenous application of methyl JA to the roots markedly decreased the performance of both root herbivores, whereas abscisic acid and the ethylene precursor 1-aminocyclopropane-1-carboxylic acid did not have any effe...</div></div></div><ul class="InlineList u-ph0x u-fs13"><li class="InlineList-item logged_in_only"><div class="share_on_academia_work_button"><a class="academia_share Button Button--inverseBlue Button--sm js-bookmark-button" data-academia-share="Work/74533875" data-share-source="work_strip" data-spinner="small_white_hide_contents"><i class="fa fa-plus"></i><span class="work-strip-link-text u-ml1x" data-content="button_text">Bookmark</span></a></div></li><li class="InlineList-item"><div class="download"><a id="65b27aa8de4936a28bf4e9ceeea4f29e" rel="nofollow" data-download="{"attachment_id":82651779,"asset_id":74533875,"asset_type":"Work","always_allow_download":false,"track":null,"button_location":"work_strip","source":null,"hide_modal":null}" class="Button Button--sm Button--inverseGreen js-download-button prompt_button doc_download" href="https://www.academia.edu/attachments/82651779/download_file?st=MTczMjQ1MjUxNyw4LjIyMi4yMDguMTQ2&s=work_strip"><i class="fa fa-arrow-circle-o-down fa-lg"></i><span class="u-textUppercase u-ml1x" data-content="button_text">Download</span></a></div></li><li class="InlineList-item"><ul class="InlineList InlineList--bordered u-ph0x"><li class="InlineList-item InlineList-item--bordered"><span class="InlineList-item-text">by <span itemscope="itemscope" itemprop="author" itemtype="https://schema.org/Person"><a class="u-tcGrayDark u-fw700" data-has-card-for-user="50177525" href="https://independent.academia.edu/MichaelStout1">Michael Stout</a><script data-card-contents-for-user="50177525" type="text/json">{"id":50177525,"first_name":"Michael","last_name":"Stout","domain_name":"independent","page_name":"MichaelStout1","display_name":"Michael Stout","profile_url":"https://independent.academia.edu/MichaelStout1?f_ri=3243133","photo":"/images/s65_no_pic.png"}</script></span></span></li><li class="js-paper-rank-work_74533875 InlineList-item InlineList-item--bordered hidden"><span class="js-paper-rank-view hidden u-tcGrayDark" data-paper-rank-work-id="74533875"><i class="u-m1x fa fa-bar-chart"></i><strong class="js-paper-rank"></strong></span><script>$(function() { new Works.PaperRankView({ workId: 74533875, container: ".js-paper-rank-work_74533875", }); 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However, very little is known about the signals that are involved in defending plants against root feeders and how they are influenced by abiotic factors. We investigated these aspects for the interaction between rice (Oryza sativa) and two root-feeding insects: the generalist cucumber beetle (Diabrotica balteata) and the more specialized rice water weevil (Lissorhoptrus oryzophilus). Rice plants responded to root attack by increasing the production of jasmonic acid (JA) and abscisic acid, whereas in contrast to in herbivore-attacked leaves, salicylic acid and ethylene levels remained unchanged. The JA response was decoupled from flooding and remained constant over different soil moisture levels. Exogenous application of methyl JA to the roots markedly decreased the performance of both root herbivores, whereas abscisic acid and the ethylene precursor 1-aminocyclopropane-1-carboxylic acid did not have any effe...","downloadable_attachments":[{"id":82651779,"asset_id":74533875,"asset_type":"Work","always_allow_download":false}],"ordered_authors":[{"id":50177525,"first_name":"Michael","last_name":"Stout","domain_name":"independent","page_name":"MichaelStout1","display_name":"Michael Stout","profile_url":"https://independent.academia.edu/MichaelStout1?f_ri=3243133","photo":"/images/s65_no_pic.png"}],"research_interests":[{"id":2215,"name":"Water","url":"https://www.academia.edu/Documents/in/Water?f_ri=3243133","nofollow":false},{"id":5411,"name":"Biomass","url":"https://www.academia.edu/Documents/in/Biomass?f_ri=3243133","nofollow":false},{"id":32923,"name":"Gene 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href="https://www.academia.edu/46716924/Seed_Germination_and_Vigor">Seed Germination and Vigor</a></div></div><div class="u-pb4x u-mt3x"></div><ul class="InlineList u-ph0x u-fs13"><li class="InlineList-item logged_in_only"><div class="share_on_academia_work_button"><a class="academia_share Button Button--inverseBlue Button--sm js-bookmark-button" data-academia-share="Work/46716924" data-share-source="work_strip" data-spinner="small_white_hide_contents"><i class="fa fa-plus"></i><span class="work-strip-link-text u-ml1x" data-content="button_text">Bookmark</span></a></div></li><li class="InlineList-item"><ul class="InlineList InlineList--bordered u-ph0x"><li class="InlineList-item InlineList-item--bordered"><span class="InlineList-item-text">by <span itemscope="itemscope" itemprop="author" itemtype="https://schema.org/Person"><a class="u-tcGrayDark u-fw700" data-has-card-for-user="41627458" href="https://independent.academia.edu/ManuelDuval">Manuel Duval</a><script 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type="text/json">{"id":43761,"name":"Transcriptome","url":"https://www.academia.edu/Documents/in/Transcriptome?f_ri=3243133","nofollow":false}</script><a class="InlineList-item-text" data-has-card-for-ri="115090" href="https://www.academia.edu/Documents/in/Plant_Growth_Regulators">Plant Growth Regulators</a>, <script data-card-contents-for-ri="115090" type="text/json">{"id":115090,"name":"Plant Growth Regulators","url":"https://www.academia.edu/Documents/in/Plant_Growth_Regulators?f_ri=3243133","nofollow":false}</script><a class="InlineList-item-text" data-has-card-for-ri="165000" href="https://www.academia.edu/Documents/in/Desiccation">Desiccation</a><script data-card-contents-for-ri="165000" type="text/json">{"id":165000,"name":"Desiccation","url":"https://www.academia.edu/Documents/in/Desiccation?f_ri=3243133","nofollow":false}</script></span></li><script>(function(){ if (true) { new Aedu.ResearchInterestListCard({ el: $('*[data-has-card-for-ri-list=46716924]'), work: 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itemtype="https://schema.org/ScholarlyArticle"><div class="header"><div class="title u-fontSerif u-fs22 u-lineHeight1_3"><a class="u-tcGrayDarkest js-work-link" href="https://www.academia.edu/63333505/Both_the_Jasmonic_Acid_and_the_Salicylic_Acid_Pathways_Contribute_to_Resistance_to_the_Biotrophic_Clubroot_Agent_Plasmodiophora_brassicae_in_Arabidopsis">Both the Jasmonic Acid and the Salicylic Acid Pathways Contribute to Resistance to the Biotrophic Clubroot Agent Plasmodiophora brassicae in Arabidopsis</a></div></div><div class="u-pb4x u-mt3x"><div class="summary u-fs14 u-fw300 u-lineHeight1_5 u-tcGrayDarkest"><div class="summarized">The role of salicylic acid (SA) and jasmonic acid (JA) signaling in resistance to root pathogens has been poorly documented. We assessed the contribution of SA and JA to basal and partial resistance of Arabidopsis to the biotrophic... <a class="more_link u-tcGrayDark u-linkUnstyled" data-container=".work_63333505" data-show=".complete" data-hide=".summarized" data-more-link-behavior="true" href="#">more</a></div><div class="complete hidden">The role of salicylic acid (SA) and jasmonic acid (JA) signaling in resistance to root pathogens has been poorly documented. We assessed the contribution of SA and JA to basal and partial resistance of Arabidopsis to the biotrophic clubroot agent Plasmodiophora brassicae. SA and JA levels as well as the expression of the SA-responsive genes PR2 and PR5 and the JA-responsive genes ARGAH2 and THI2.1 were monitored in infected roots of the accessions Col-0 (susceptible) and Bur-0 (partially resistant). SA signaling was activated in Bur-0 but not in Col-0. The JA pathway was weakly activated in Bur-0 but was strongly induced in Col-0. The contribution of both pathways to clubroot resistance was then assessed using exogenous phytohormone application and mutants affected in SA or JA signaling. Exogenous SA treatment decreased clubroot symptoms in the two Arabidopsis accessions, whereas JA treatment reduced clubroot symptoms only in Col-0. The cpr5-2 mutant, in which SA responses are const...</div></div></div><ul class="InlineList u-ph0x u-fs13"><li class="InlineList-item logged_in_only"><div class="share_on_academia_work_button"><a class="academia_share Button Button--inverseBlue Button--sm js-bookmark-button" data-academia-share="Work/63333505" data-share-source="work_strip" data-spinner="small_white_hide_contents"><i class="fa fa-plus"></i><span class="work-strip-link-text u-ml1x" data-content="button_text">Bookmark</span></a></div></li><li class="InlineList-item"><div class="download"><a id="f05332d2ff03ec3be128ae2e1de344c5" rel="nofollow" data-download="{"attachment_id":75798800,"asset_id":63333505,"asset_type":"Work","always_allow_download":false,"track":null,"button_location":"work_strip","source":null,"hide_modal":null}" class="Button Button--sm Button--inverseGreen js-download-button prompt_button doc_download" href="https://www.academia.edu/attachments/75798800/download_file?st=MTczMjQ1MjUxNyw4LjIyMi4yMDguMTQ2&s=work_strip"><i class="fa fa-arrow-circle-o-down fa-lg"></i><span class="u-textUppercase u-ml1x" data-content="button_text">Download</span></a></div></li><li class="InlineList-item"><ul class="InlineList InlineList--bordered u-ph0x"><li class="InlineList-item InlineList-item--bordered"><span class="InlineList-item-text">by <span itemscope="itemscope" itemprop="author" itemtype="https://schema.org/Person"><a class="u-tcGrayDark u-fw700" data-has-card-for-user="56986566" href="https://independent.academia.edu/MelanieJubault">Mélanie Jubault</a><script data-card-contents-for-user="56986566" type="text/json">{"id":56986566,"first_name":"Mélanie","last_name":"Jubault","domain_name":"independent","page_name":"MelanieJubault","display_name":"Mélanie Jubault","profile_url":"https://independent.academia.edu/MelanieJubault?f_ri=3243133","photo":"/images/s65_no_pic.png"}</script></span></span></li><li class="js-paper-rank-work_63333505 InlineList-item InlineList-item--bordered hidden"><span class="js-paper-rank-view hidden u-tcGrayDark" data-paper-rank-work-id="63333505"><i class="u-m1x fa fa-bar-chart"></i><strong class="js-paper-rank"></strong></span><script>$(function() { new Works.PaperRankView({ workId: 63333505, container: ".js-paper-rank-work_63333505", }); 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We assessed the contribution of SA and JA to basal and partial resistance of Arabidopsis to the biotrophic clubroot agent Plasmodiophora brassicae. SA and JA levels as well as the expression of the SA-responsive genes PR2 and PR5 and the JA-responsive genes ARGAH2 and THI2.1 were monitored in infected roots of the accessions Col-0 (susceptible) and Bur-0 (partially resistant). SA signaling was activated in Bur-0 but not in Col-0. The JA pathway was weakly activated in Bur-0 but was strongly induced in Col-0. The contribution of both pathways to clubroot resistance was then assessed using exogenous phytohormone application and mutants affected in SA or JA signaling. Exogenous SA treatment decreased clubroot symptoms in the two Arabidopsis accessions, whereas JA treatment reduced clubroot symptoms only in Col-0. 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container.find('.percentile-widget').removeClass('hidden'); }); });</script></li><li class="js-view-count-work_47768320 InlineList-item InlineList-item--bordered hidden"><div><span><span class="js-view-count view-count u-mr2x" data-work-id="47768320"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 47768320; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=47768320]").text(description); $(".js-view-count-work_47768320").attr('title', description).tooltip(); }); });</script></span><script>$(function() { $(".js-view-count-work_47768320").removeClass('hidden') })</script></div></li><li class="InlineList-item u-positionRelative" style="max-width: 250px"><div class="u-positionAbsolute" data-has-card-for-ri-list="47768320"><i class="fa fa-tag InlineList-item-icon u-positionRelative"></i>  <a class="InlineList-item-text u-positionRelative">20</a>  </div><span class="InlineList-item-text u-textTruncate u-pl10x"><a class="InlineList-item-text" data-has-card-for-ri="4306" href="https://www.academia.edu/Documents/in/Pest_Management">Pest Management</a>, <script data-card-contents-for-ri="4306" type="text/json">{"id":4306,"name":"Pest Management","url":"https://www.academia.edu/Documents/in/Pest_Management?f_ri=3243133","nofollow":false}</script><a class="InlineList-item-text" data-has-card-for-ri="9846" href="https://www.academia.edu/Documents/in/Ecology">Ecology</a>, <script data-card-contents-for-ri="9846" type="text/json">{"id":9846,"name":"Ecology","url":"https://www.academia.edu/Documents/in/Ecology?f_ri=3243133","nofollow":false}</script><a class="InlineList-item-text" data-has-card-for-ri="48303" href="https://www.academia.edu/Documents/in/Colonization">Colonization</a>, <script data-card-contents-for-ri="48303" type="text/json">{"id":48303,"name":"Colonization","url":"https://www.academia.edu/Documents/in/Colonization?f_ri=3243133","nofollow":false}</script><a class="InlineList-item-text" data-has-card-for-ri="79747" href="https://www.academia.edu/Documents/in/Colonisation">Colonisation</a><script data-card-contents-for-ri="79747" type="text/json">{"id":79747,"name":"Colonisation","url":"https://www.academia.edu/Documents/in/Colonisation?f_ri=3243133","nofollow":false}</script></span></li><script>(function(){ if (true) { new Aedu.ResearchInterestListCard({ el: $('*[data-has-card-for-ri-list=47768320]'), work: {"id":47768320,"title":"Exogenous application of methyl jasmonate elicits defenses in Norway spruce (Picea abies) and reduces host colonization by the bark beetle Ips typographus","created_at":"2021-04-28T07:04:23.806-07:00","url":"https://www.academia.edu/47768320/Exogenous_application_of_methyl_jasmonate_elicits_defenses_in_Norway_spruce_Picea_abies_and_reduces_host_colonization_by_the_bark_beetle_Ips_typographus?f_ri=3243133","dom_id":"work_47768320","summary":null,"downloadable_attachments":[{"id":66709999,"asset_id":47768320,"asset_type":"Work","always_allow_download":false}],"ordered_authors":[{"id":90674,"first_name":"Nadir","last_name":"Erbilgin","domain_name":"ualberta","page_name":"NadirErbilgin","display_name":"Nadir Erbilgin","profile_url":"https://ualberta.academia.edu/NadirErbilgin?f_ri=3243133","photo":"/images/s65_no_pic.png"}],"research_interests":[{"id":4306,"name":"Pest Management","url":"https://www.academia.edu/Documents/in/Pest_Management?f_ri=3243133","nofollow":false},{"id":9846,"name":"Ecology","url":"https://www.academia.edu/Documents/in/Ecology?f_ri=3243133","nofollow":false},{"id":48303,"name":"Colonization","url":"https://www.academia.edu/Documents/in/Colonization?f_ri=3243133","nofollow":false},{"id":79747,"name":"Colonisation","url":"https://www.academia.edu/Documents/in/Colonisation?f_ri=3243133","nofollow":false},{"id":99234,"name":"Animals","url":"https://www.academia.edu/Documents/in/Animals?f_ri=3243133"},{"id":115090,"name":"Plant Growth Regulators","url":"https://www.academia.edu/Documents/in/Plant_Growth_Regulators?f_ri=3243133"},{"id":223041,"name":"Oecologia","url":"https://www.academia.edu/Documents/in/Oecologia?f_ri=3243133"},{"id":242013,"name":"TERPENE","url":"https://www.academia.edu/Documents/in/TERPENE?f_ri=3243133"},{"id":242015,"name":"PLANT DEFENSE","url":"https://www.academia.edu/Documents/in/PLANT_DEFENSE?f_ri=3243133"},{"id":274327,"name":"Beetles","url":"https://www.academia.edu/Documents/in/Beetles?f_ri=3243133"},{"id":289517,"name":"Bark Beetle","url":"https://www.academia.edu/Documents/in/Bark_Beetle?f_ri=3243133"},{"id":289519,"name":"Ips typographus","url":"https://www.academia.edu/Documents/in/Ips_typographus?f_ri=3243133"},{"id":362142,"name":"Picea","url":"https://www.academia.edu/Documents/in/Picea?f_ri=3243133"},{"id":576520,"name":"Picea abies","url":"https://www.academia.edu/Documents/in/Picea_abies?f_ri=3243133"},{"id":700960,"name":"Norway Spruce","url":"https://www.academia.edu/Documents/in/Norway_Spruce?f_ri=3243133"},{"id":880714,"name":"Induced Defense","url":"https://www.academia.edu/Documents/in/Induced_Defense?f_ri=3243133"},{"id":911001,"name":"Methyl Jasmonate","url":"https://www.academia.edu/Documents/in/Methyl_Jasmonate?f_ri=3243133"},{"id":2471742,"name":"Dry Weight","url":"https://www.academia.edu/Documents/in/Dry_Weight?f_ri=3243133"},{"id":2645023,"name":"Host","url":"https://www.academia.edu/Documents/in/Host?f_ri=3243133"},{"id":3243133,"name":"Oxylipins","url":"https://www.academia.edu/Documents/in/Oxylipins?f_ri=3243133"}]}, }) } })();</script></ul></li></ul></div></div><div class="u-borderBottom1 u-borderColorGrayLighter"><div class="clearfix u-pv7x u-mb0x js-work-card work_47562072" data-work_id="47562072" itemscope="itemscope" itemtype="https://schema.org/ScholarlyArticle"><div class="header"><div class="title u-fontSerif u-fs22 u-lineHeight1_3"><a class="u-tcGrayDarkest js-work-link" href="https://www.academia.edu/47562072/Quantitative_peptidomics_study_reveals_that_a_wound_induced_peptide_from_PR_1_regulates_immune_signaling_in_tomato">Quantitative peptidomics study reveals that a wound-induced peptide from PR-1 regulates immune signaling in tomato</a></div></div><div class="u-pb4x u-mt3x"><div class="summary u-fs14 u-fw300 u-lineHeight1_5 u-tcGrayDarkest"><div class="summarized">Many important cell-to-cell communication events in multicellular organisms are mediated by peptides, but only a few peptides have been identified in plants. In an attempt to address the difficulties in identifying plant signaling... <a class="more_link u-tcGrayDark u-linkUnstyled" data-container=".work_47562072" data-show=".complete" data-hide=".summarized" data-more-link-behavior="true" href="#">more</a></div><div class="complete hidden">Many important cell-to-cell communication events in multicellular organisms are mediated by peptides, but only a few peptides have been identified in plants. In an attempt to address the difficulties in identifying plant signaling peptides, we developed a novel peptidomics approach and used this approach to discover defense signaling peptides in plants. In addition to the canonical peptide systemin, several novel peptides were confidently identified in tomato (Solanum lycopersicum) and quantified to be induced by both wounding and methyl jasmonate (MeJA). A wounding or wounding plus MeJA-induced peptide derived from the pathogenesis-related protein 1 (PR-1) family was found to induce significant antipathogen and minor antiherbivore responses in tomato. This study highlights a role for PR-1 in immune signaling and suggests the potential application of plant endogenous peptides in efforts to defeat biological threats in crop production. As PR-1 is highly conserved across many organism...</div></div></div><ul class="InlineList u-ph0x u-fs13"><li class="InlineList-item logged_in_only"><div class="share_on_academia_work_button"><a class="academia_share Button Button--inverseBlue Button--sm js-bookmark-button" data-academia-share="Work/47562072" data-share-source="work_strip" data-spinner="small_white_hide_contents"><i class="fa fa-plus"></i><span class="work-strip-link-text u-ml1x" data-content="button_text">Bookmark</span></a></div></li><li class="InlineList-item"><div class="download"><a id="78abc9eb4bec11f8f9dfbb2cb982d492" rel="nofollow" data-download="{"attachment_id":66591312,"asset_id":47562072,"asset_type":"Work","always_allow_download":false,"track":null,"button_location":"work_strip","source":null,"hide_modal":null}" class="Button Button--sm Button--inverseGreen js-download-button prompt_button doc_download" href="https://www.academia.edu/attachments/66591312/download_file?st=MTczMjQ1MjUxNyw4LjIyMi4yMDguMTQ2&s=work_strip"><i class="fa fa-arrow-circle-o-down fa-lg"></i><span class="u-textUppercase u-ml1x" data-content="button_text">Download</span></a></div></li><li class="InlineList-item"><ul class="InlineList InlineList--bordered u-ph0x"><li class="InlineList-item InlineList-item--bordered"><span class="InlineList-item-text">by <span itemscope="itemscope" itemprop="author" itemtype="https://schema.org/Person"><a class="u-tcGrayDark u-fw700" data-has-card-for-user="109753274" href="https://independent.academia.edu/RongNanHuang">Rong Nan Huang</a><script data-card-contents-for-user="109753274" type="text/json">{"id":109753274,"first_name":"Rong Nan","last_name":"Huang","domain_name":"independent","page_name":"RongNanHuang","display_name":"Rong Nan Huang","profile_url":"https://independent.academia.edu/RongNanHuang?f_ri=3243133","photo":"/images/s65_no_pic.png"}</script></span></span></li><li class="js-paper-rank-work_47562072 InlineList-item InlineList-item--bordered hidden"><span class="js-paper-rank-view hidden u-tcGrayDark" data-paper-rank-work-id="47562072"><i class="u-m1x fa fa-bar-chart"></i><strong class="js-paper-rank"></strong></span><script>$(function() { new Works.PaperRankView({ workId: 47562072, container: ".js-paper-rank-work_47562072", }); });</script></li><li class="js-percentile-work_47562072 InlineList-item InlineList-item--bordered hidden u-tcGrayDark"><span class="percentile-widget hidden"><span class="u-mr2x percentile-widget" style="display: none">•</span><span class="u-mr2x work-percentile"></span></span><script>$(function () { var workId = 47562072; window.Academia.workPercentilesFetcher.queue(workId, function (percentileText) { var container = $(".js-percentile-work_47562072"); container.find('.work-percentile').text(percentileText.charAt(0).toUpperCase() + percentileText.slice(1)); container.find('.percentile-widget').show(); container.find('.percentile-widget').removeClass('hidden'); }); });</script></li><li class="js-view-count-work_47562072 InlineList-item InlineList-item--bordered hidden"><div><span><span class="js-view-count view-count u-mr2x" data-work-id="47562072"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 47562072; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=47562072]").text(description); $(".js-view-count-work_47562072").attr('title', description).tooltip(); }); });</script></span><script>$(function() { $(".js-view-count-work_47562072").removeClass('hidden') })</script></div></li><li class="InlineList-item u-positionRelative" style="max-width: 250px"><div class="u-positionAbsolute" data-has-card-for-ri-list="47562072"><i class="fa fa-tag InlineList-item-icon u-positionRelative"></i>  <a class="InlineList-item-text u-positionRelative">20</a>  </div><span class="InlineList-item-text u-textTruncate u-pl10x"><a class="InlineList-item-text" data-has-card-for-ri="156" href="https://www.academia.edu/Documents/in/Genetics">Genetics</a>, <script data-card-contents-for-ri="156" type="text/json">{"id":156,"name":"Genetics","url":"https://www.academia.edu/Documents/in/Genetics?f_ri=3243133","nofollow":false}</script><a class="InlineList-item-text" data-has-card-for-ri="5541" href="https://www.academia.edu/Documents/in/Plant_Biology">Plant Biology</a>, <script data-card-contents-for-ri="5541" type="text/json">{"id":5541,"name":"Plant Biology","url":"https://www.academia.edu/Documents/in/Plant_Biology?f_ri=3243133","nofollow":false}</script><a class="InlineList-item-text" data-has-card-for-ri="9786" href="https://www.academia.edu/Documents/in/Proteomics">Proteomics</a>, <script data-card-contents-for-ri="9786" type="text/json">{"id":9786,"name":"Proteomics","url":"https://www.academia.edu/Documents/in/Proteomics?f_ri=3243133","nofollow":false}</script><a class="InlineList-item-text" data-has-card-for-ri="66973" href="https://www.academia.edu/Documents/in/Plant_diseases">Plant diseases</a><script data-card-contents-for-ri="66973" type="text/json">{"id":66973,"name":"Plant diseases","url":"https://www.academia.edu/Documents/in/Plant_diseases?f_ri=3243133","nofollow":false}</script></span></li><script>(function(){ if (true) { new Aedu.ResearchInterestListCard({ el: $('*[data-has-card-for-ri-list=47562072]'), work: {"id":47562072,"title":"Quantitative peptidomics study reveals that a wound-induced peptide from PR-1 regulates immune signaling in tomato","created_at":"2021-04-23T03:59:19.879-07:00","url":"https://www.academia.edu/47562072/Quantitative_peptidomics_study_reveals_that_a_wound_induced_peptide_from_PR_1_regulates_immune_signaling_in_tomato?f_ri=3243133","dom_id":"work_47562072","summary":"Many important cell-to-cell communication events in multicellular organisms are mediated by peptides, but only a few peptides have been identified in plants. In an attempt to address the difficulties in identifying plant signaling peptides, we developed a novel peptidomics approach and used this approach to discover defense signaling peptides in plants. In addition to the canonical peptide systemin, several novel peptides were confidently identified in tomato (Solanum lycopersicum) and quantified to be induced by both wounding and methyl jasmonate (MeJA). A wounding or wounding plus MeJA-induced peptide derived from the pathogenesis-related protein 1 (PR-1) family was found to induce significant antipathogen and minor antiherbivore responses in tomato. This study highlights a role for PR-1 in immune signaling and suggests the potential application of plant endogenous peptides in efforts to defeat biological threats in crop production. As PR-1 is highly conserved across many organism...","downloadable_attachments":[{"id":66591312,"asset_id":47562072,"asset_type":"Work","always_allow_download":false}],"ordered_authors":[{"id":109753274,"first_name":"Rong Nan","last_name":"Huang","domain_name":"independent","page_name":"RongNanHuang","display_name":"Rong Nan Huang","profile_url":"https://independent.academia.edu/RongNanHuang?f_ri=3243133","photo":"/images/s65_no_pic.png"}],"research_interests":[{"id":156,"name":"Genetics","url":"https://www.academia.edu/Documents/in/Genetics?f_ri=3243133","nofollow":false},{"id":5541,"name":"Plant Biology","url":"https://www.academia.edu/Documents/in/Plant_Biology?f_ri=3243133","nofollow":false},{"id":9786,"name":"Proteomics","url":"https://www.academia.edu/Documents/in/Proteomics?f_ri=3243133","nofollow":false},{"id":66973,"name":"Plant diseases","url":"https://www.academia.edu/Documents/in/Plant_diseases?f_ri=3243133","nofollow":false},{"id":105062,"name":"Disease resistance","url":"https://www.academia.edu/Documents/in/Disease_resistance?f_ri=3243133"},{"id":115090,"name":"Plant Growth Regulators","url":"https://www.academia.edu/Documents/in/Plant_Growth_Regulators?f_ri=3243133"},{"id":151086,"name":"Peptides","url":"https://www.academia.edu/Documents/in/Peptides?f_ri=3243133"},{"id":225787,"name":"High Performance Liquid Chromatography","url":"https://www.academia.edu/Documents/in/High_Performance_Liquid_Chromatography?f_ri=3243133"},{"id":277229,"name":"Pseudomonas Syringae","url":"https://www.academia.edu/Documents/in/Pseudomonas_Syringae?f_ri=3243133"},{"id":350931,"name":"Mechanical Stress","url":"https://www.academia.edu/Documents/in/Mechanical_Stress?f_ri=3243133"},{"id":743643,"name":"Host Pathogen Interactions","url":"https://www.academia.edu/Documents/in/Host_Pathogen_Interactions?f_ri=3243133"},{"id":809881,"name":"Amino Acid Sequence","url":"https://www.academia.edu/Documents/in/Amino_Acid_Sequence?f_ri=3243133"},{"id":1035050,"name":"Proteome","url":"https://www.academia.edu/Documents/in/Proteome?f_ri=3243133"},{"id":1181939,"name":"PLANT PROTEINS","url":"https://www.academia.edu/Documents/in/PLANT_PROTEINS?f_ri=3243133"},{"id":1640340,"name":"Lycopersicon esculentum","url":"https://www.academia.edu/Documents/in/Lycopersicon_esculentum?f_ri=3243133"},{"id":1681026,"name":"Biochemistry and cell biology","url":"https://www.academia.edu/Documents/in/Biochemistry_and_cell_biology?f_ri=3243133"},{"id":1905343,"name":"Plant Leaves","url":"https://www.academia.edu/Documents/in/Plant_Leaves?f_ri=3243133"},{"id":2467566,"name":"Molecular Sequence Data","url":"https://www.academia.edu/Documents/in/Molecular_Sequence_Data?f_ri=3243133"},{"id":3067128,"name":"reverse transcriptase polymerase chain reaction","url":"https://www.academia.edu/Documents/in/reverse_transcriptase_polymerase_chain_reaction?f_ri=3243133"},{"id":3243133,"name":"Oxylipins","url":"https://www.academia.edu/Documents/in/Oxylipins?f_ri=3243133"}]}, }) } })();</script></ul></li></ul></div></div><div class="u-borderBottom1 u-borderColorGrayLighter"><div class="clearfix u-pv7x u-mb0x js-work-card work_46976328" data-work_id="46976328" itemscope="itemscope" itemtype="https://schema.org/ScholarlyArticle"><div class="header"><div class="title u-fontSerif u-fs22 u-lineHeight1_3"><a class="u-tcGrayDarkest js-work-link" href="https://www.academia.edu/46976328/Weights_in_the_Balance_Jasmonic_Acid_and_Salicylic_Acid_Signaling_in_Root_Biotroph_Interactions">Weights in the Balance: Jasmonic Acid and Salicylic Acid Signaling in Root-Biotroph Interactions</a></div></div><div class="u-pb4x u-mt3x"><div class="summary u-fs14 u-fw300 u-lineHeight1_5 u-tcGrayDarkest"><div class="summarized">Work on the interaction of aerial plant parts with pathogens has identified the signaling molecules jasmonic acid (JA) and salicylic acid (SA) as important players in induced defense of the plant against invading organisms. Much less is... <a class="more_link u-tcGrayDark u-linkUnstyled" data-container=".work_46976328" data-show=".complete" data-hide=".summarized" data-more-link-behavior="true" href="#">more</a></div><div class="complete hidden">Work on the interaction of aerial plant parts with pathogens has identified the signaling molecules jasmonic acid (JA) and salicylic acid (SA) as important players in induced defense of the plant against invading organisms. Much less is known about the role of JA and SA signaling in root infection. Recent progress has been made in research on plant interactions with biotrophic mutualists and parasites that exclusively associate with roots, namely arbuscular mycorrhizal and rhizobial symbioses on one hand and nematode and parasitic plant interactions on the other hand. Here, we review these recent advances relating JA and SA signaling to specific stages of root colonization and discuss how both signaling molecules contribute to a balance between compatibility and defense in mutualistic as well as parasitic biotroph-root interactions.</div></div></div><ul class="InlineList u-ph0x u-fs13"><li class="InlineList-item logged_in_only"><div class="share_on_academia_work_button"><a class="academia_share Button Button--inverseBlue Button--sm js-bookmark-button" data-academia-share="Work/46976328" data-share-source="work_strip" data-spinner="small_white_hide_contents"><i class="fa fa-plus"></i><span class="work-strip-link-text u-ml1x" data-content="button_text">Bookmark</span></a></div></li><li class="InlineList-item"><div class="download"><a id="4e3221735bfaecf0048243670ff3688d" rel="nofollow" data-download="{"attachment_id":66317771,"asset_id":46976328,"asset_type":"Work","always_allow_download":false,"track":null,"button_location":"work_strip","source":null,"hide_modal":null}" class="Button Button--sm Button--inverseGreen js-download-button prompt_button doc_download" href="https://www.academia.edu/attachments/66317771/download_file?st=MTczMjQ1MjUxNyw4LjIyMi4yMDguMTQ2&s=work_strip"><i class="fa fa-arrow-circle-o-down fa-lg"></i><span class="u-textUppercase u-ml1x" data-content="button_text">Download</span></a></div></li><li class="InlineList-item"><ul class="InlineList InlineList--bordered u-ph0x"><li class="InlineList-item InlineList-item--bordered"><span class="InlineList-item-text">by <span itemscope="itemscope" itemprop="author" itemtype="https://schema.org/Person"><a class="u-tcGrayDark u-fw700" data-has-card-for-user="65961625" href="https://independent.academia.edu/UtaPaszkowski">Uta Paszkowski</a><script data-card-contents-for-user="65961625" type="text/json">{"id":65961625,"first_name":"Uta","last_name":"Paszkowski","domain_name":"independent","page_name":"UtaPaszkowski","display_name":"Uta Paszkowski","profile_url":"https://independent.academia.edu/UtaPaszkowski?f_ri=3243133","photo":"/images/s65_no_pic.png"}</script></span></span></li><li class="js-paper-rank-work_46976328 InlineList-item InlineList-item--bordered hidden"><span class="js-paper-rank-view hidden u-tcGrayDark" data-paper-rank-work-id="46976328"><i class="u-m1x fa fa-bar-chart"></i><strong class="js-paper-rank"></strong></span><script>$(function() { new Works.PaperRankView({ workId: 46976328, container: ".js-paper-rank-work_46976328", }); 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Much less is known about the role of JA and SA signaling in root infection. Recent progress has been made in research on plant interactions with biotrophic mutualists and parasites that exclusively associate with roots, namely arbuscular mycorrhizal and rhizobial symbioses on one hand and nematode and parasitic plant interactions on the other hand. 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Data","url":"https://www.academia.edu/Documents/in/Molecular_Sequence_Data?f_ri=3243133"},{"id":3243133,"name":"Oxylipins","url":"https://www.academia.edu/Documents/in/Oxylipins?f_ri=3243133"}]}, }) } })();</script></ul></li></ul></div></div><div class="u-borderBottom1 u-borderColorGrayLighter"><div class="clearfix u-pv7x u-mb0x js-work-card work_82076873" data-work_id="82076873" itemscope="itemscope" itemtype="https://schema.org/ScholarlyArticle"><div class="header"><div class="title u-fontSerif u-fs22 u-lineHeight1_3"><a class="u-tcGrayDarkest js-work-link" href="https://www.academia.edu/82076873/Induced_Systemic_Resistance_in_Arabidopsis_thaliana_in_Response_to_Root_Inoculation_with_Pseudomonas_fluorescens_CHA0">Induced Systemic Resistance in Arabidopsis thaliana in Response to Root Inoculation with Pseudomonas fluorescens CHA0</a></div></div><div class="u-pb4x u-mt3x"><div class="summary u-fs14 u-fw300 u-lineHeight1_5 u-tcGrayDarkest"><div class="summarized">Root inoculation of Arabidopsis thaliana ecotype Columbia with Pseudomonas fluorescens CHA0r partially protected leaves from the oomycete Peronospora parasitica. The molecular determinants of Pseudomonas fluorescens CHA0r for this induced... <a class="more_link u-tcGrayDark u-linkUnstyled" data-container=".work_82076873" data-show=".complete" data-hide=".summarized" data-more-link-behavior="true" href="#">more</a></div><div class="complete hidden">Root inoculation of Arabidopsis thaliana ecotype Columbia with Pseudomonas fluorescens CHA0r partially protected leaves from the oomycete Peronospora parasitica. The molecular determinants of Pseudomonas fluorescens CHA0r for this induced systemic resistance (ISR) were investigated, using mutants derived from strain CHA0: CHA400 (pyoverdine deficient), CHA805 (exoprotease deficient), CHA77 (HCN deficient), CHA660 (pyoluteorin deficient), CHA631 (2,4-diacetylphloroglucinol [DAPG] deficient), and CHA89 (HCN, DAPG- and pyoluteorin deficient). Only mutations interfering with DAPG production led to a significant decrease in ISR to Peronospora parasitica. Thus, DAPG production in Pseudomonas fluorescens is required for the induction of ISR to Peronospora parasitica. DAPG is known for its antibiotic activity; however, our data indicate that one action of DAPG could be due to an effect on the physiology of the plant. DAPG at 10 to 100 μM applied to roots of Arabidopsis mimicked the ISR effe...</div></div></div><ul class="InlineList u-ph0x u-fs13"><li class="InlineList-item logged_in_only"><div class="share_on_academia_work_button"><a class="academia_share Button Button--inverseBlue Button--sm js-bookmark-button" data-academia-share="Work/82076873" data-share-source="work_strip" data-spinner="small_white_hide_contents"><i class="fa fa-plus"></i><span class="work-strip-link-text u-ml1x" data-content="button_text">Bookmark</span></a></div></li><li class="InlineList-item"><div class="download"><a id="66a6dd2132e6b1e0eb0e509dbaac052f" rel="nofollow" data-download="{"attachment_id":87897979,"asset_id":82076873,"asset_type":"Work","always_allow_download":false,"track":null,"button_location":"work_strip","source":null,"hide_modal":null}" class="Button Button--sm Button--inverseGreen js-download-button prompt_button doc_download" href="https://www.academia.edu/attachments/87897979/download_file?st=MTczMjQ1MjUxNyw4LjIyMi4yMDguMTQ2&s=work_strip"><i class="fa fa-arrow-circle-o-down fa-lg"></i><span class="u-textUppercase u-ml1x" data-content="button_text">Download</span></a></div></li><li class="InlineList-item"><ul class="InlineList InlineList--bordered u-ph0x"><li class="InlineList-item InlineList-item--bordered"><span class="InlineList-item-text">by <span itemscope="itemscope" itemprop="author" itemtype="https://schema.org/Person"><a class="u-tcGrayDark u-fw700" data-has-card-for-user="57099926" href="https://independent.academia.edu/JeanpierreM%C3%A9traux">Jean-pierre Métraux</a><script data-card-contents-for-user="57099926" type="text/json">{"id":57099926,"first_name":"Jean-pierre","last_name":"Métraux","domain_name":"independent","page_name":"JeanpierreMétraux","display_name":"Jean-pierre Métraux","profile_url":"https://independent.academia.edu/JeanpierreM%C3%A9traux?f_ri=3243133","photo":"/images/s65_no_pic.png"}</script></span></span></li><li class="js-paper-rank-work_82076873 InlineList-item InlineList-item--bordered hidden"><span class="js-paper-rank-view hidden u-tcGrayDark" data-paper-rank-work-id="82076873"><i class="u-m1x fa fa-bar-chart"></i><strong class="js-paper-rank"></strong></span><script>$(function() { new Works.PaperRankView({ workId: 82076873, container: ".js-paper-rank-work_82076873", }); 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The molecular determinants of Pseudomonas fluorescens CHA0r for this induced systemic resistance (ISR) were investigated, using mutants derived from strain CHA0: CHA400 (pyoverdine deficient), CHA805 (exoprotease deficient), CHA77 (HCN deficient), CHA660 (pyoluteorin deficient), CHA631 (2,4-diacetylphloroglucinol [DAPG] deficient), and CHA89 (HCN, DAPG- and pyoluteorin deficient). Only mutations interfering with DAPG production led to a significant decrease in ISR to Peronospora parasitica. Thus, DAPG production in Pseudomonas fluorescens is required for the induction of ISR to Peronospora parasitica. DAPG is known for its antibiotic activity; however, our data indicate that one action of DAPG could be due to an effect on the physiology of the plant. DAPG at 10 to 100 μM applied to roots of Arabidopsis mimicked the ISR effe...","downloadable_attachments":[{"id":87897979,"asset_id":82076873,"asset_type":"Work","always_allow_download":false}],"ordered_authors":[{"id":57099926,"first_name":"Jean-pierre","last_name":"Métraux","domain_name":"independent","page_name":"JeanpierreMétraux","display_name":"Jean-pierre Métraux","profile_url":"https://independent.academia.edu/JeanpierreM%C3%A9traux?f_ri=3243133","photo":"/images/s65_no_pic.png"}],"research_interests":[{"id":156,"name":"Genetics","url":"https://www.academia.edu/Documents/in/Genetics?f_ri=3243133","nofollow":false},{"id":159,"name":"Microbiology","url":"https://www.academia.edu/Documents/in/Microbiology?f_ri=3243133","nofollow":false},{"id":5541,"name":"Plant 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Acid","url":"https://www.academia.edu/Documents/in/Salicylic_Acid?f_ri=3243133"},{"id":1752942,"name":"Induced Resistance","url":"https://www.academia.edu/Documents/in/Induced_Resistance?f_ri=3243133"},{"id":2021170,"name":"Spodoptera litura","url":"https://www.academia.edu/Documents/in/Spodoptera_litura?f_ri=3243133"},{"id":3243133,"name":"Oxylipins","url":"https://www.academia.edu/Documents/in/Oxylipins?f_ri=3243133"}]}, }) } })();</script></ul></li></ul></div></div><div class="u-borderBottom1 u-borderColorGrayLighter"><div class="clearfix u-pv7x u-mb0x js-work-card work_74079669" data-work_id="74079669" itemscope="itemscope" itemtype="https://schema.org/ScholarlyArticle"><div class="header"><div class="title u-fontSerif u-fs22 u-lineHeight1_3"><a class="u-tcGrayDarkest js-work-link" href="https://www.academia.edu/74079669/Independent_Preharvest_Applications_of_Methyl_Jasmonate_and_Chitosan_Elicit_Differential_Upregulation_of_Defense_Related_Genes_with_Reduced_Incidence_of_Gray_Mold_Decay_during_Postharvest_Storage_of_Fragaria_chiloensis_Fruit">Independent Preharvest Applications of Methyl Jasmonate and Chitosan Elicit Differential Upregulation of Defense-Related Genes with Reduced Incidence of Gray Mold Decay during Postharvest Storage of Fragaria chiloensis Fruit</a></div></div><div class="u-pb4x u-mt3x"><div class="summary u-fs14 u-fw300 u-lineHeight1_5 u-tcGrayDarkest"><div class="summarized">The Chilean strawberry (Fragaria chiloensis) fruit has interesting organoleptic properties, but its postharvest life is affected by gray mold decay caused by Botrytis cinerea. The effect of preharvest applications of methyl jasmonate... <a class="more_link u-tcGrayDark u-linkUnstyled" data-container=".work_74079669" data-show=".complete" data-hide=".summarized" data-more-link-behavior="true" href="#">more</a></div><div class="complete hidden">The Chilean strawberry (Fragaria chiloensis) fruit has interesting organoleptic properties, but its postharvest life is affected by gray mold decay caused by Botrytis cinerea. The effect of preharvest applications of methyl jasmonate (MeJA) or chitosan on the molecular defense-related responses and protection against gray mold decay were investigated in Chilean strawberry fruit during postharvest storage. Specifically, we inoculated harvested fruit with B. cinerea spores and studied the expression of genes encoding for the pathogenesis-related (PR) proteins β-1,3-glucanases (FcBG2-1, FcBG2-2 and FcBG2-3) and chitinases (FcCHI2-2 and FcCHI3-1), and for polygalacturonase inhibiting proteins (FcPGIP1 and FcPGIP2) at 0, 2, 24, 48, and 72 h post inoculation (hpi). Remarkably, MeJA- and chitosan-treated fruit exhibited a lower incidence of B. cinerea infection than the control-treated at 48 and 72 hpi. At the molecular level, both are efficient elicitors for priming in F. chiloensis fruit...</div></div></div><ul class="InlineList u-ph0x u-fs13"><li class="InlineList-item logged_in_only"><div class="share_on_academia_work_button"><a class="academia_share Button Button--inverseBlue Button--sm js-bookmark-button" data-academia-share="Work/74079669" data-share-source="work_strip" data-spinner="small_white_hide_contents"><i class="fa fa-plus"></i><span class="work-strip-link-text u-ml1x" data-content="button_text">Bookmark</span></a></div></li><li class="InlineList-item"><div class="download"><a id="e562fb31b30af14fe1b413417dc6f598" rel="nofollow" data-download="{"attachment_id":82361516,"asset_id":74079669,"asset_type":"Work","always_allow_download":false,"track":null,"button_location":"work_strip","source":null,"hide_modal":null}" class="Button Button--sm Button--inverseGreen js-download-button prompt_button doc_download" href="https://www.academia.edu/attachments/82361516/download_file?st=MTczMjQ1MjUxNyw4LjIyMi4yMDguMTQ2&s=work_strip"><i class="fa fa-arrow-circle-o-down fa-lg"></i><span class="u-textUppercase u-ml1x" data-content="button_text">Download</span></a></div></li><li class="InlineList-item"><ul class="InlineList InlineList--bordered u-ph0x"><li class="InlineList-item InlineList-item--bordered"><span class="InlineList-item-text">by <span itemscope="itemscope" itemprop="author" itemtype="https://schema.org/Person"><a class="u-tcGrayDark u-fw700" data-has-card-for-user="57960629" href="https://independent.academia.edu/EugenioSanfuentes">Eugenio Sanfuentes</a><script data-card-contents-for-user="57960629" type="text/json">{"id":57960629,"first_name":"Eugenio","last_name":"Sanfuentes","domain_name":"independent","page_name":"EugenioSanfuentes","display_name":"Eugenio Sanfuentes","profile_url":"https://independent.academia.edu/EugenioSanfuentes?f_ri=3243133","photo":"https://0.academia-photos.com/57960629/26563135/25099297/s65_eugenio.sanfuentes.jpg"}</script></span></span></li><li class="js-paper-rank-work_74079669 InlineList-item InlineList-item--bordered hidden"><span class="js-paper-rank-view hidden u-tcGrayDark" data-paper-rank-work-id="74079669"><i class="u-m1x fa fa-bar-chart"></i><strong class="js-paper-rank"></strong></span><script>$(function() { new Works.PaperRankView({ workId: 74079669, container: ".js-paper-rank-work_74079669", }); 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The effect of preharvest applications of methyl jasmonate (MeJA) or chitosan on the molecular defense-related responses and protection against gray mold decay were investigated in Chilean strawberry fruit during postharvest storage. Specifically, we inoculated harvested fruit with B. cinerea spores and studied the expression of genes encoding for the pathogenesis-related (PR) proteins β-1,3-glucanases (FcBG2-1, FcBG2-2 and FcBG2-3) and chitinases (FcCHI2-2 and FcCHI3-1), and for polygalacturonase inhibiting proteins (FcPGIP1 and FcPGIP2) at 0, 2, 24, 48, and 72 h post inoculation (hpi). Remarkably, MeJA- and chitosan-treated fruit exhibited a lower incidence of B. cinerea infection than the control-treated at 48 and 72 hpi. At the molecular level, both are efficient elicitors for priming in F. chiloensis fruit...","downloadable_attachments":[{"id":82361516,"asset_id":74079669,"asset_type":"Work","always_allow_download":false}],"ordered_authors":[{"id":57960629,"first_name":"Eugenio","last_name":"Sanfuentes","domain_name":"independent","page_name":"EugenioSanfuentes","display_name":"Eugenio 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to the Hemibiotrophic Fungal Pathogen Colletotrichum higginsianum</a></div></div><div class="u-pb4x u-mt3x"><div class="summary u-fs14 u-fw300 u-lineHeight1_5 u-tcGrayDarkest"><div class="summarized">When challenged with the crucifer pathogen Colletotrichum higginsianum, Arabidopsis thaliana ecotype Columbia (Col-0) was colonized by the fungus within 2 to 3 days, developing brown necrotic lesions surrounded by a yellow halo. Lesions... <a class="more_link u-tcGrayDark u-linkUnstyled" data-container=".work_61315351" data-show=".complete" data-hide=".summarized" data-more-link-behavior="true" href="#">more</a></div><div class="complete hidden">When challenged with the crucifer pathogen Colletotrichum higginsianum, Arabidopsis thaliana ecotype Columbia (Col-0) was colonized by the fungus within 2 to 3 days, developing brown necrotic lesions surrounded by a yellow halo. Lesions spread from the inoculation site within 3 to 4 days, and subsequently continued to expand until they covered the entire leaf. Electron microscopy confirmed that C. higginsianum is a hemibiotroph on Arabidopsis, feeding initially on living cells as a biotroph before switching to a necrotrophic mode of growth. A collection of 37 ecotypes of Arabidopsis varied in their responses to infection by C. higginsianum. The ecotype Eil-0 was highly resistant, with symptoms limited to necrotic flecking and with only very limited fungal colonization. Analyses suggested that the hypersensitive response and reactive oxygen species may be important in this defense response. Expression analyses with cDNA microarrays indicated that the defense reaction depends primaril...</div></div></div><ul class="InlineList u-ph0x u-fs13"><li class="InlineList-item logged_in_only"><div class="share_on_academia_work_button"><a class="academia_share Button Button--inverseBlue Button--sm js-bookmark-button" data-academia-share="Work/61315351" data-share-source="work_strip" data-spinner="small_white_hide_contents"><i class="fa fa-plus"></i><span class="work-strip-link-text u-ml1x" data-content="button_text">Bookmark</span></a></div></li><li class="InlineList-item"><div class="download"><a id="b9429b7511f40d68867825bda4002e09" rel="nofollow" data-download="{"attachment_id":74379741,"asset_id":61315351,"asset_type":"Work","always_allow_download":false,"track":null,"button_location":"work_strip","source":null,"hide_modal":null}" class="Button Button--sm Button--inverseGreen js-download-button prompt_button doc_download" href="https://www.academia.edu/attachments/74379741/download_file?st=MTczMjQ1MjUxOCw4LjIyMi4yMDguMTQ2&s=work_strip"><i class="fa fa-arrow-circle-o-down fa-lg"></i><span class="u-textUppercase u-ml1x" data-content="button_text">Download</span></a></div></li><li class="InlineList-item"><ul class="InlineList InlineList--bordered u-ph0x"><li class="InlineList-item InlineList-item--bordered"><span class="InlineList-item-text">by <span itemscope="itemscope" itemprop="author" itemtype="https://schema.org/Person"><a class="u-tcGrayDark u-fw700" data-has-card-for-user="203020022" href="https://independent.academia.edu/THirayama">Takashi Hirayama</a><script data-card-contents-for-user="203020022" type="text/json">{"id":203020022,"first_name":"Takashi","last_name":"Hirayama","domain_name":"independent","page_name":"THirayama","display_name":"Takashi Hirayama","profile_url":"https://independent.academia.edu/THirayama?f_ri=3243133","photo":"https://0.academia-photos.com/203020022/64049142/52364740/s65_takashi.hirayama.png"}</script></span></span></li><li class="js-paper-rank-work_61315351 InlineList-item InlineList-item--bordered hidden"><span class="js-paper-rank-view hidden u-tcGrayDark" data-paper-rank-work-id="61315351"><i class="u-m1x fa fa-bar-chart"></i><strong class="js-paper-rank"></strong></span><script>$(function() { new Works.PaperRankView({ workId: 61315351, container: ".js-paper-rank-work_61315351", }); 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Lesions spread from the inoculation site within 3 to 4 days, and subsequently continued to expand until they covered the entire leaf. Electron microscopy confirmed that C. higginsianum is a hemibiotroph on Arabidopsis, feeding initially on living cells as a biotroph before switching to a necrotrophic mode of growth. A collection of 37 ecotypes of Arabidopsis varied in their responses to infection by C. higginsianum. The ecotype Eil-0 was highly resistant, with symptoms limited to necrotic flecking and with only very limited fungal colonization. Analyses suggested that the hypersensitive response and reactive oxygen species may be important in this defense response. 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