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poly(ADP-ribose) polymerase 1 (PARP1)</title> <meta name="description" content="Search results for: poly(ADP-ribose) polymerase 1 (PARP1)"> <meta name="keywords" content="poly(ADP-ribose) polymerase 1 (PARP1)"> <meta name="viewport" content="width=device-width, initial-scale=1, minimum-scale=1, maximum-scale=1, user-scalable=no"> <meta charset="utf-8"> <link href="https://cdn.waset.org/favicon.ico" type="image/x-icon" rel="shortcut icon"> <link href="https://cdn.waset.org/static/plugins/bootstrap-4.2.1/css/bootstrap.min.css" rel="stylesheet"> <link href="https://cdn.waset.org/static/plugins/fontawesome/css/all.min.css" rel="stylesheet"> <link href="https://cdn.waset.org/static/css/site.css?v=150220211555" rel="stylesheet"> </head> <body> <header> <div class="container"> <nav class="navbar navbar-expand-lg navbar-light"> <a class="navbar-brand" href="https://waset.org"> <img src="https://cdn.waset.org/static/images/wasetc.png" alt="Open Science Research Excellence" title="Open Science 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method="get" action="https://publications.waset.org/abstracts/search"> <div id="custom-search-input"> <div class="input-group"> <i class="fas fa-search"></i> <input type="text" class="search-query" name="q" placeholder="Author, Title, Abstract, Keywords" value="poly(ADP-ribose) polymerase 1 (PARP1)"> <input type="submit" class="btn_search" value="Search"> </div> </div> </form> </div> </div> <div class="row mt-3"> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Commenced</strong> in January 2007</div> </div> </div> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Frequency:</strong> Monthly</div> </div> </div> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Edition:</strong> International</div> </div> </div> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Paper Count:</strong> 279</div> </div> </div> </div> <h1 class="mt-3 mb-3 text-center" style="font-size:1.6rem;">Search results for: poly(ADP-ribose) polymerase 1 (PARP1)</h1> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">279</span> PARP1 Links Transcription of a Subset of RBL2-Dependent Genes with Cell Cycle Progression</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Ewelina%20Wisnik">Ewelina Wisnik</a>, <a href="https://publications.waset.org/abstracts/search?q=Zsolt%20Regdon"> Zsolt Regdon</a>, <a href="https://publications.waset.org/abstracts/search?q=Kinga%20Chmielewska"> Kinga Chmielewska</a>, <a href="https://publications.waset.org/abstracts/search?q=Laszlo%20Virag"> Laszlo Virag</a>, <a href="https://publications.waset.org/abstracts/search?q=Agnieszka%20Robaszkiewicz"> Agnieszka Robaszkiewicz</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Apart from protecting genome, PARP1 has been documented to regulate many intracellular processes inter alia gene transcription by physically interacting with chromatin bound proteins and by their ADP-ribosylation. Our recent findings indicate that expression of PARP1 decreases during the differentiation of human CD34+ hematopoietic stem cells to monocytes as a consequence of differentiation-associated cell growth arrest and formation of E2F4-RBL2-HDAC1-SWI/SNF repressive complex at the promoter of this gene. Since the RBL2 complexes repress genes in a E2F-dependent manner and are widespread in the genome in G0 arrested cells, we asked (a) if RBL2 directly contributes to defining monocyte phenotype and function by targeting gene promoters and (b) if RBL2 controls gene transcription indirectly by repressing PARP1. For identification of genes controlled by RBL2 and/or PARP1,we used primer libraries for surface receptors and TLR signaling mediators, genes were silenced by siRNA or shRNA, analysis of gene promoter occupation by selected proteins was carried out by ChIP-qPCR, while statistical analysis in GraphPad Prism 5 and STATISTICA, ChIP-Seq data were analysed in Galaxy 2.5.0.0. On the list of 28 genes regulated by RBL2, we identified only four solely repressed by RBL2-E2F4-HDAC1-BRM complex. Surprisingly, 24 out of 28 emerged genes controlled by RBL2 were co-regulated by PARP1 in six different manners. In one mode of RBL2/PARP1 co-operation, represented by MAP2K6 and MAPK3, PARP1 was found to associate with gene promoters upon RBL2 silencing, which was previously shown to restore PARP1 expression in monocytes. PARP1 effect on gene transcription was observed only in the presence of active EP300, which acetylated gene promoters and activated transcription. Further analysis revealed that PARP1 binding to MA2K6 and MAPK3 promoters enabled recruitment of EP300 in monocytes, while in proliferating cancer cell lines, which actively transcribe PARP1, this protein maintained EP300 at the promoters of MA2K6 and MAPK3. Genome-wide analysis revealed a similar distribution of PARP1 and EP300 around transcription start sites and the co-occupancy of some gene promoters by PARP1 and EP300 in cancer cells. Here, we described a new RBL2/PARP1/EP300 axis which controls gene transcription regardless of the cell type. In this model cell, cycle-dependent transcription of PARP1 regulates expression of some genes repressed by RBL2 upon cell cycle limitation. Thus, RBL2 may indirectly regulate transcription of some genes by controlling the expression of EP300-recruiting PARP1. Acknowledgement: This work was financed by Polish National Science Centre grants nr DEC-2013/11/D/NZ2/00033 and DEC-2015/19/N/NZ2/01735. L.V. is funded by the National Research, Development and Innovation Office grants GINOP-2.3.2-15-2016-00020 TUMORDNS, GINOP-2.3.2-15-2016-00048-STAYALIVE and OTKA K112336. AR is supported by Polish Ministry of Science and Higher Education 776/STYP/11/2016. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=retinoblastoma%20transcriptional%20co-repressor%20like%202%20%28RBL2%29" title="retinoblastoma transcriptional co-repressor like 2 (RBL2)">retinoblastoma transcriptional co-repressor like 2 (RBL2)</a>, <a href="https://publications.waset.org/abstracts/search?q=poly%28ADP-ribose%29%20polymerase%201%20%28PARP1%29" title=" poly(ADP-ribose) polymerase 1 (PARP1)"> poly(ADP-ribose) polymerase 1 (PARP1)</a>, <a href="https://publications.waset.org/abstracts/search?q=E1A%20binding%20protein%20p300%20%28EP300%29" title=" E1A binding protein p300 (EP300)"> E1A binding protein p300 (EP300)</a>, <a href="https://publications.waset.org/abstracts/search?q=monocytes" title=" monocytes"> monocytes</a> </p> <a href="https://publications.waset.org/abstracts/79896/parp1-links-transcription-of-a-subset-of-rbl2-dependent-genes-with-cell-cycle-progression" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/79896.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">209</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">278</span> ECOSURF EH3 - A Taq DNA Polymerase Enhancer</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Kimberley%20Phoena%20Fan">Kimberley Phoena Fan</a>, <a href="https://publications.waset.org/abstracts/search?q=Yu%20Zhang"> Yu Zhang</a> </p> <p class="card-text"><strong>Abstract:</strong></p> ECOSURF™ EH-3 Surfactant (EH3) is a nonionic surfactant and has superior wetting and excellent oil removal properties. It is biodegradable with low toxicity and meets or exceeds US EPA Design for the Environment Criteria, and is widely used as a home cleaner, commercial and industrial degreaser. We have recently found that EH3 also possesses a special function which is characterized as an enhancer to Taq DNA polymerase and ameliorator to reduce the effects of PCR inhibitors, i.e., blood, urea, Guanidinium thiocyanate, Humic acids, polyphenol, and Polysaccharides. This is a new kind of PCR enhancer that does not work on relieving secondary structures of GC-rich templates. We have compared EH3’s effects on Taq DNA Polymerase along with other well-known enhancers, such as DMSO, betaine, and BSA, using GC rich or deficient template and found that, unlike DMSO and Betaine, the EH3 boosting effect on PCR reaction is not through reducing Tm. The results show the same increase of PCR products regardless of the GC contents or secondary structures. The mechanism of EH3 enhancing PCR is through its direct interaction with or stimulation of the DNA polymerase and making the enzymes more resistant to inhibitors in the presence of EH3. This phenomenon has first been observed for EH3, a new type of PCR enzyme enhancer. Subsequent research also shows that a series of similar surfactants boost Taq DNA polymerase as well. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=EH3" title="EH3">EH3</a>, <a href="https://publications.waset.org/abstracts/search?q=DNA" title=" DNA"> DNA</a>, <a href="https://publications.waset.org/abstracts/search?q=polymerase" title=" polymerase"> polymerase</a>, <a href="https://publications.waset.org/abstracts/search?q=enhancer" title=" enhancer"> enhancer</a>, <a href="https://publications.waset.org/abstracts/search?q=raw%20biological%20samples" title=" raw biological samples"> raw biological samples</a> </p> <a href="https://publications.waset.org/abstracts/157679/ecosurf-eh3-a-taq-dna-polymerase-enhancer" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/157679.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">139</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">277</span> Tenofovir-Amino Acid Conjugates Act as Polymerase Substrates: Implications for Avoiding Cellular Phosphorylation in the Discovery of Nucleotide Analogs</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Weijie%20Gu">Weijie Gu</a>, <a href="https://publications.waset.org/abstracts/search?q=Sergio%20Martinez"> Sergio Martinez</a>, <a href="https://publications.waset.org/abstracts/search?q=Hoai%20Nguyen"> Hoai Nguyen</a>, <a href="https://publications.waset.org/abstracts/search?q=Hongtao%20Xu"> Hongtao Xu</a>, <a href="https://publications.waset.org/abstracts/search?q=Piet%20Herdewijn"> Piet Herdewijn</a>, <a href="https://publications.waset.org/abstracts/search?q=Steven%20De%20Jonghe"> Steven De Jonghe</a>, <a href="https://publications.waset.org/abstracts/search?q=Kalyan%20Das"> Kalyan Das</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Nucleotide analogs are used for treating viral infections such as HIV, hepatitis B, hepatitis C, influenza, and SARS-CoV-2. To become polymerase substrates, a nucleotide analog must be phosphorylated by cellular kinases, which are rate-limiting. The goal of this study is to develop dNTP/NTP analogs directly from nucleotides. Tenofovir (TFV) analogs were synthesized by conjugating with natural or unnatural amino acids. It demonstrates that some conjugates act as dNTP analogs, and HIV-1 reverse transcriptase (RT) catalytically incorporates the TFV part as the chain terminator. X-ray structures in complex with HIV-1 RT/dsDNA showed binding of the conjugates at the polymerase active site, however, in different modes in the presence of Mg²⁺ vs. Mn²⁺ ions. The adaptability of the compounds is seemingly essential for catalytic incorporation of TFV by RT. 4d with a carboxyl sidechain demonstrated the highest incorporation. 4e showed weak incorporation and rather behaved as a dNTP-competitive inhibitor. This result advocates the feasibility of designing NTP/dNTP analogs by chemical substitutions to nucleotide analogs. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=dNTP%20analogs" title="dNTP analogs">dNTP analogs</a>, <a href="https://publications.waset.org/abstracts/search?q=nucleotide%20analogs" title=" nucleotide analogs"> nucleotide analogs</a>, <a href="https://publications.waset.org/abstracts/search?q=polymerase" title=" polymerase"> polymerase</a>, <a href="https://publications.waset.org/abstracts/search?q=tenofovir" title=" tenofovir"> tenofovir</a>, <a href="https://publications.waset.org/abstracts/search?q=X-ray%20structure" title=" X-ray structure"> X-ray structure</a> </p> <a href="https://publications.waset.org/abstracts/130804/tenofovir-amino-acid-conjugates-act-as-polymerase-substrates-implications-for-avoiding-cellular-phosphorylation-in-the-discovery-of-nucleotide-analogs" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/130804.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">153</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">276</span> Comparison of Sensitivity and Specificity of Pap Smear and Polymerase Chain Reaction Methods for Detection of Human Papillomavirus: A Review of Literature</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=M.%20Malekian">M. Malekian</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20E.%20Heydari"> M. E. Heydari</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20Irani%20Estyar"> M. Irani Estyar</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Human papillomavirus (HPV) is one of the most common sexually transmitted infection, which may lead to cervical cancer as the main cause of it. With early diagnosis and treatment in health care services, cervical cancer and its complications are considered to be preventable. This study was aimed to compare the efficiency, sensitivity, and specificity of Pap smear and polymerase chain reaction (PCR) in detecting HPV. A literature search was performed in Google Scholar, PubMed and SID databases using the keywords 'human papillomavirus', 'pap smear' and 'polymerase change reaction' to identify studies comparing Pap smear and PCR methods for the detection. No restrictions were considered.10 studies were included in this review. All samples that were positive by pop smear were also positive by PCR. However, there were positive samples detected by PCR which was negative by pop smear and in all studies, many positive samples were missed by pop smear technique. Although The Pap smear had high specificity, PCR based HPV detection was more sensitive method and had the highest sensitivity. In order to promote the quality of detection and high achievement of the maximum results, PCR diagnostic methods in addition to the Pap smear are needed and Pap smear method should be combined with PCR techniques according to the high error rate of Pap smear in detection. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=human%20papillomavirus" title="human papillomavirus">human papillomavirus</a>, <a href="https://publications.waset.org/abstracts/search?q=cervical%20cancer" title=" cervical cancer"> cervical cancer</a>, <a href="https://publications.waset.org/abstracts/search?q=pap%20smear" title=" pap smear"> pap smear</a>, <a href="https://publications.waset.org/abstracts/search?q=polymerase%20chain%20reaction" title=" polymerase chain reaction"> polymerase chain reaction</a> </p> <a href="https://publications.waset.org/abstracts/111248/comparison-of-sensitivity-and-specificity-of-pap-smear-and-polymerase-chain-reaction-methods-for-detection-of-human-papillomavirus-a-review-of-literature" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/111248.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">131</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">275</span> Structural Insights into the Bypass of the Major Deaminated Purines by Translesion Synthesis DNA Polymerase</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Hunmin%20Jung">Hunmin Jung</a>, <a href="https://publications.waset.org/abstracts/search?q=Michael%20Hawkins"> Michael Hawkins</a>, <a href="https://publications.waset.org/abstracts/search?q=Seongmin%20Lee"> Seongmin Lee</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The exocyclic amines of nucleobases can undergo deamination by various DNA damaging agents such as reactive oxygen species, nitric oxide, and water. The deamination of guanine and adenine generates the promutagenic xanthine and hypoxanthine, respectively. The exocyclic amines of bases in DNA are hydrogen bond donors, while the carbonyl moiety generated by the base deamination acts as hydrogen bond acceptors, which can alter base pairing properties of the purines. Xanthine is known to base pair with both cytosine and thymine, while hypoxanthine predominantly pairs with cytosine to promote A to G mutations. Despite the known promutagenicity of the major deaminated purines, structures of DNA polymerase bypassing these lesions have not been reported. To gain insights into the deaminated-induced mutagenesis, we solved crystal structures of human DNA polymerase η (polη) catalyzing across xanthine and hypoxanthine. In the catalytic site of polη, the deaminated guanine (i.e., xanthine) forms three Watson-Crick-like hydrogen bonds with an incoming dCTP, indicating the O2-enol tautomer of xanthine involves in the base pairing. The formation of the enol tautomer appears to be promoted by the minor groove contact by Gln38 of polη. When hypoxanthine is at the templating position, the deaminated adenine uses its O6-keto tautomer to form two Watson-Crick hydrogen bonds with an incoming dCTP, providing the structural basis for the high promutagenicity of hypoxanthine. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=DNA%20damage" title="DNA damage">DNA damage</a>, <a href="https://publications.waset.org/abstracts/search?q=DNA%20polymerase" title="DNA polymerase">DNA polymerase</a>, <a href="https://publications.waset.org/abstracts/search?q=deamination" title="deamination">deamination</a>, <a href="https://publications.waset.org/abstracts/search?q=mutagenesis" title="mutagenesis">mutagenesis</a>, <a href="https://publications.waset.org/abstracts/search?q=tautomerization" title="tautomerization">tautomerization</a>, <a href="https://publications.waset.org/abstracts/search?q=translesion%20synthesis" title="translesion synthesis">translesion synthesis</a> </p> <a href="https://publications.waset.org/abstracts/149816/structural-insights-into-the-bypass-of-the-major-deaminated-purines-by-translesion-synthesis-dna-polymerase" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/149816.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">134</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">274</span> A Small-Molecular Inhibitor of Influenza Virus via Disrupting the PA and PB1 Interaction of the Viral Polymerase</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Shuofeng%20Yuan">Shuofeng Yuan</a>, <a href="https://publications.waset.org/abstracts/search?q=Bojian%20Zheng"> Bojian Zheng</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Assembly of the heterotrimeric polymerase complex of influenza virus from the individual subunits PB1, PA, and PB2 is a prerequisite for viral replication, in which the interaction between the N-terminal of PB1 (PB1N) and the C terminal of PA (PAC) may be a desired target for antiviral development. In this study, we first compared the feasibility of high throughput screening by enzyme-linked immunosorbent assay (ELISA) and fluorescence polarization (FP) assay. Among the two, ELISA was demonstrated to own broader dynamic range so that it was used for screening inhibitors, which blocked PA and PB1 interaction. Several binding inhibitors of PAC-PB1N were identified and subsequently tested for the antiviral efficacy. Apparently, 3-(2-chlorophenyl)-6-ethyl-7-methyl[1,2,4]triazolo[4,3-a]pyrimidin-5-ol, designated ANA-1, was found to be a strong inhibitor of PAC-PB1N interaction and act as a potent antiviral agent against the infections of multiple subtypes of influenza A virus, including H1N1, H3N2, H5N1, H7N7, H7N9 and H9N2 subtypes, in cell cultures. Intranasal administration of ANA-1 protected mice from lethal challenge and reduced lung viral loads in H1N1 virus infected BALB/c mice. Docking analyses predicted that ANA-1 bound to an allosteric site of PAC, which would cause conformational changes thereby disrupting the PAC-PB1N interaction. Overall, our study has identified a novel compound with potential to be developed as an anti-influenza drug. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=influenza" title="influenza">influenza</a>, <a href="https://publications.waset.org/abstracts/search?q=antiviral" title=" antiviral"> antiviral</a>, <a href="https://publications.waset.org/abstracts/search?q=viral%20polymerase" title=" viral polymerase"> viral polymerase</a>, <a href="https://publications.waset.org/abstracts/search?q=compounds" title=" compounds"> compounds</a> </p> <a href="https://publications.waset.org/abstracts/38070/a-small-molecular-inhibitor-of-influenza-virus-via-disrupting-the-pa-and-pb1-interaction-of-the-viral-polymerase" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/38070.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">347</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">273</span> The Influence of the Moving Speeds of DNA Droplet on Polymerase Chain Reaction</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Jyh%20Jyh%20Chen">Jyh Jyh Chen</a>, <a href="https://publications.waset.org/abstracts/search?q=Fu%20H.%20Yang"> Fu H. Yang</a>, <a href="https://publications.waset.org/abstracts/search?q=Chen%20W.%20Wang"> Chen W. Wang</a>, <a href="https://publications.waset.org/abstracts/search?q=Yu%20M.%20Lin"> Yu M. Lin</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In this work, a reaction chamber is reciprocated among three temperature regions by using an oscillatory thermal cycling machine. Three cartridge heaters are collocated to heat three aluminum blocks in order to achieve PCR requirements in the reaction chamber. The effects of various chamber moving speeds among different temperature regions on the chamber temperature profiles are presented. To solve the evaporation effect of the sample in the PCR experiment, the mineral oil and the cover lid are used. The influences of various extension times on DNA amplification are also demonstrated. The target fragments of the amplification are 385-bp and 420-bp. The results show when the forward speed is set at 6 mm/s and the backward speed is 2.4 mm/s, the temperature required for the experiment can be achieved. It is successful to perform the amplification of DNA fragments in our device. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=oscillatory" title="oscillatory">oscillatory</a>, <a href="https://publications.waset.org/abstracts/search?q=polymerase%20chain%20reaction" title=" polymerase chain reaction"> polymerase chain reaction</a>, <a href="https://publications.waset.org/abstracts/search?q=reaction%20chamber" title=" reaction chamber"> reaction chamber</a>, <a href="https://publications.waset.org/abstracts/search?q=thermal%20cycling%20machine" title=" thermal cycling machine"> thermal cycling machine</a> </p> <a href="https://publications.waset.org/abstracts/64588/the-influence-of-the-moving-speeds-of-dna-droplet-on-polymerase-chain-reaction" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/64588.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">530</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">272</span> Cdk1 Gates Cell Cycle-Dependent tRNA Synthesis by Regulating RNA Polymerase III Activity</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Maricarmen%20Herrera">Maricarmen Herrera</a>, <a href="https://publications.waset.org/abstracts/search?q=Pierre%20Chymkowitch"> Pierre Chymkowitch</a>, <a href="https://publications.waset.org/abstracts/search?q=Joe%20Robertson"> Joe Robertson</a>, <a href="https://publications.waset.org/abstracts/search?q=Jens%20Eriksson"> Jens Eriksson</a>, <a href="https://publications.waset.org/abstracts/search?q=Jorrit%20Enserink"> Jorrit Enserink</a> </p> <p class="card-text"><strong>Abstract:</strong></p> tRNA genes are transcribed by RNA polymerase III. During recent years, it has become clear that tDNA transcription fluctuates during the cell cycle. However, the mechanism by which the cell cycle controls the amplitude of tDNA transcription remains unknown. We found that the cyclin Clb5 recruits the cyclin dependent kinase Cdk1 to tRNA genes to sharply increase tRNA synthesis during a brief interval in the cell cycle. We show that Cdk1 promotes the interaction of TFIIIB with TFIIIC, that it stimulates the recruitment of TFIIIC to tRNA genes, that it prevents the formation of an overly stable TFIIIB-tDNA complex and that it augments the dynamics of RNA polymerase III. Furthermore, we identify Bdp1 as a novel Cdk1 substrate, and phosphorylation of Bdp1 is required for the cell cycle-dependent increase in tDNA transcription. In addition, we show that phosphorylation of the Cdk1 substrate Nup60 mediates formation of a Nup60-Nup2 complex at tRNA genes, which is also required for cell cycle-dependent tDNA transcription. Together, our findings indicate that Cdk1 activity gates tRNA synthesis by regulating the dynamics of the TFIIIB-TFIIIC-RNAPIII complex, and that it may promote the formation of a nuclear pore microenvironment conducive to efficient tDNA transcription. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Cdk1" title="Cdk1">Cdk1</a>, <a href="https://publications.waset.org/abstracts/search?q=cell%20cycle" title=" cell cycle"> cell cycle</a>, <a href="https://publications.waset.org/abstracts/search?q=RNAPIII%20machinery" title=" RNAPIII machinery"> RNAPIII machinery</a>, <a href="https://publications.waset.org/abstracts/search?q=tRNA" title=" tRNA"> tRNA</a> </p> <a href="https://publications.waset.org/abstracts/77416/cdk1-gates-cell-cycle-dependent-trna-synthesis-by-regulating-rna-polymerase-iii-activity" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/77416.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">181</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">271</span> Use of a New Multiplex Quantitative Polymerase Chain Reaction Based Assay for Simultaneous Detection of Neisseria Meningitidis, Escherichia Coli K1, Streptococcus agalactiae, and Streptococcus pneumoniae</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Nastaran%20Hemmati">Nastaran Hemmati</a>, <a href="https://publications.waset.org/abstracts/search?q=Farhad%20Nikkhahi"> Farhad Nikkhahi</a>, <a href="https://publications.waset.org/abstracts/search?q=Amir%20Javadi"> Amir Javadi</a>, <a href="https://publications.waset.org/abstracts/search?q=Sahar%20Eskandarion"> Sahar Eskandarion</a>, <a href="https://publications.waset.org/abstracts/search?q=Seyed%20Mahmuod%20%20Amin%20Marashi"> Seyed Mahmuod Amin Marashi</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Neisseria meningitidis, Escherichia coli K, Streptococcus agalactiae, and Streptococcus pneumoniae cause 90% of bacterial meningitis. Almost all infected people die or have irreversible neurological complications. Therefore, it is essential to have a diagnostic kit with the ability to quickly detect these fatal infections. The project involved 212 patients from whom cerebrospinal fluid samples were obtained. After total genome extraction and performing multiplex quantitative polymerase chain reaction (qPCR), the presence or absence of each infectious factor was determined by comparing with standard strains. The specificity, sensitivity, positive predictive value, and negative predictive value calculated were 100%, 92.9%, 50%, and 100%, respectively. So, due to the high specificity and sensitivity of the designed primers, they can be used instead of bacterial culture that takes at least 24 to 48 hours. The remarkable benefit of this method is associated with the speed (up to 3 hours) at which the procedure could be completed. It is also worth noting that this method can reduce the personnel unintentional errors which may occur in the laboratory. On the other hand, as this method simultaneously identifies four common factors that cause bacterial meningitis, it could be used as an auxiliary method diagnostic technique in laboratories particularly in cases of emergency medicine. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=cerebrospinal%20fluid" title="cerebrospinal fluid">cerebrospinal fluid</a>, <a href="https://publications.waset.org/abstracts/search?q=meningitis" title=" meningitis"> meningitis</a>, <a href="https://publications.waset.org/abstracts/search?q=quantitative%20polymerase%20chain%20reaction" title=" quantitative polymerase chain reaction"> quantitative polymerase chain reaction</a>, <a href="https://publications.waset.org/abstracts/search?q=simultaneous%20detection" title=" simultaneous detection"> simultaneous detection</a>, <a href="https://publications.waset.org/abstracts/search?q=diagnosis%20testing" title=" diagnosis testing"> diagnosis testing</a> </p> <a href="https://publications.waset.org/abstracts/151315/use-of-a-new-multiplex-quantitative-polymerase-chain-reaction-based-assay-for-simultaneous-detection-of-neisseria-meningitidis-escherichia-coli-k1-streptococcus-agalactiae-and-streptococcus-pneumoniae" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/151315.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">116</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">270</span> PTFE Capillary-Based DNA Amplification within an Oscillatory Thermal Cycling Device</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Jyh%20J.%20Chen">Jyh J. Chen</a>, <a href="https://publications.waset.org/abstracts/search?q=Fu%20H.%20Yang"> Fu H. Yang</a>, <a href="https://publications.waset.org/abstracts/search?q=Ming%20H.%20Liao"> Ming H. Liao</a> </p> <p class="card-text"><strong>Abstract:</strong></p> This study describes a capillary-based device integrated with the heating and cooling modules for polymerase chain reaction (PCR). The device consists of the reaction polytetrafluoroethylene (PTFE) capillary, the aluminum blocks, and is equipped with two cartridge heaters, a thermoelectric (TE) cooler, a fan, and some thermocouples for temperature control. The cartridge heaters are placed into the heating blocks and maintained at two different temperatures to achieve the denaturation and the extension step. Some thermocouples inserted into the capillary are used to obtain the transient temperature profiles of the reaction sample during thermal cycles. A 483-bp DNA template is amplified successfully in the designed system and the traditional thermal cycler. This work should be interesting to persons involved in the high-temperature based reactions and genomics or cell analysis. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=polymerase%20chain%20reaction" title="polymerase chain reaction">polymerase chain reaction</a>, <a href="https://publications.waset.org/abstracts/search?q=thermal%20cycles" title=" thermal cycles"> thermal cycles</a>, <a href="https://publications.waset.org/abstracts/search?q=capillary" title=" capillary"> capillary</a>, <a href="https://publications.waset.org/abstracts/search?q=TE%20cooler" title=" TE cooler"> TE cooler</a> </p> <a href="https://publications.waset.org/abstracts/7439/ptfe-capillary-based-dna-amplification-within-an-oscillatory-thermal-cycling-device" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/7439.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">455</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">269</span> Molecular Comparison of HEV Isolates from Sewage & Humans at Western India</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Nidhi%20S.%20Chandra">Nidhi S. Chandra</a>, <a href="https://publications.waset.org/abstracts/search?q=Veena%20Agrawal"> Veena Agrawal</a>, <a href="https://publications.waset.org/abstracts/search?q=Debprasad%20Chattopadhyay"> Debprasad Chattopadhyay</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Background: Hepatitis E virus (HEV) is a major cause of acute viral hepatitis in developing countries. It spreads feco orally mainly due to contamination of drinking water by sewage. There is limited data on the genotypic comparison of HEV isolates from sewage water and humans. The aim of this study was to identify genotype and conduct phylogenetic analysis of HEV isolates from sewage water and humans. Materials and Methods: 14 sewage water and 60 serum samples from acute sporadic hepatitis E cases (negative for hepatitis A, B, C) were tested for HEV-RNA by nested polymerase chain reaction (RTnPCR) using primers designed with in RdRp (RNA dependent RNA polymerase) region of open reading frame-1 (ORF-1). Sequencing was done by ABI prism 310. The sequences (343 nucleotides) were compared with each other and were aligned with previously reported HEV sequences obtained from GeneBank, using Clustal W software. A Phylogenetic tree was constructed by using PHYLIP version 3.67 software. Results: HEV-RNA was detected in 49/ 60 (81.67%) serum and 5/14 (35.71%) sewage samples. The sequences obtained from 17 serums and 2 sewage specimens belonged to genotype I with 85% similarity and clustering with previously reported human HEV sequences from India. HEV isolates from human and sewage in North West India are genetically closely related to each other. Conclusion: These finding suggest that sewage acts as reservoir of HEV. Therefore it is important that measures are taken for proper waste disposal and treatment of drinking water to prevent outbreaks and epidemics due to HEV. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=hepatitis%20E%20virus" title="hepatitis E virus">hepatitis E virus</a>, <a href="https://publications.waset.org/abstracts/search?q=nested%20polymerase%20chain%20reaction" title=" nested polymerase chain reaction"> nested polymerase chain reaction</a>, <a href="https://publications.waset.org/abstracts/search?q=open%20reading%20frame-1" title=" open reading frame-1"> open reading frame-1</a>, <a href="https://publications.waset.org/abstracts/search?q=nucleotidies" title=" nucleotidies"> nucleotidies</a> </p> <a href="https://publications.waset.org/abstracts/16409/molecular-comparison-of-hev-isolates-from-sewage-humans-at-western-india" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/16409.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">377</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">268</span> Detection of Respiratory Syncytial Virus (hRSV) by PCR Technique in Lower Respiratory Tract Infection (LRTI) in Babylon City</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Amal%20Raqib%20Shameran">Amal Raqib Shameran</a>, <a href="https://publications.waset.org/abstracts/search?q=Ghanim%20Aboud%20Al-Mola"> Ghanim Aboud Al-Mola </a> </p> <p class="card-text"><strong>Abstract:</strong></p> Respiratory syncytial virus (hRSV) is the major pathogens of respiratory tract infections (RTI) among infants and children in the world. They are classified in family Paramyxoviridae and sub-family Pneumovirinae. The current work aimed to detect the role of RSV in the lower respiratory tract infection (LRTI) in Hilla, Iraq. The samples were collected from 50 children who were admitted to hospital suffering from lower respiratory tract infections (LRTI). 50 nasal and pharyngeal swabs were taken from patients at the period from January 2010 till April 2011, hospitalized in Hilla Maternity and Children Hospital. The results showed that the proportion of children infected with hRSV accounted for 24% 12/50 with lower respiratory tract infections (LRTI) when they tested by polymerase chain reaction (RT-PCR). <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=respiratory%20syncytial%20virus" title="respiratory syncytial virus">respiratory syncytial virus</a>, <a href="https://publications.waset.org/abstracts/search?q=respiratory%20tract%20infections" title=" respiratory tract infections"> respiratory tract infections</a>, <a href="https://publications.waset.org/abstracts/search?q=infants" title=" infants"> infants</a>, <a href="https://publications.waset.org/abstracts/search?q=polymerase%20chain%20reaction%20%28PCR%29" title=" polymerase chain reaction (PCR)"> polymerase chain reaction (PCR)</a> </p> <a href="https://publications.waset.org/abstracts/12973/detection-of-respiratory-syncytial-virus-hrsv-by-pcr-technique-in-lower-respiratory-tract-infection-lrti-in-babylon-city" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/12973.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">356</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">267</span> Prerequisites for the Acquisition of Mammalian Pathogenicity by Influenza A Virus with a Prototypic Avian PB2 Gene</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Chung-Young%20Lee">Chung-Young Lee</a>, <a href="https://publications.waset.org/abstracts/search?q=Se-Hee%20Ahn"> Se-Hee Ahn</a>, <a href="https://publications.waset.org/abstracts/search?q=Ilhwan%20Kim"> Ilhwan Kim</a>, <a href="https://publications.waset.org/abstracts/search?q=Du-Min%20Go"> Du-Min Go</a>, <a href="https://publications.waset.org/abstracts/search?q=Dae-Yong%20Kim"> Dae-Yong Kim</a>, <a href="https://publications.waset.org/abstracts/search?q=Jun-Gu%20Choi"> Jun-Gu Choi</a>, <a href="https://publications.waset.org/abstracts/search?q=Youn-Jeong%20Lee"> Youn-Jeong Lee</a>, <a href="https://publications.waset.org/abstracts/search?q=Jae-Hong%20Kim"> Jae-Hong Kim</a>, <a href="https://publications.waset.org/abstracts/search?q=Hyuk-Joon%20Kwon"> Hyuk-Joon Kwon</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The polymerase of avian influenza A virus (AIV) is a heterotrimer composed of PB2, PB1 and PA. PB2 plays a role in overcoming the host barrier; however, the genetic prerequisites for avian PB2 to acquire mammalian pathogenic mutations have not been well elucidated. Here, we demonstrated that key amino acid mutations (I66M, I109V and I133V, collectively referred to as MVV) of prototypic avian PB2 increase the replication efficiency of recombinant PR8 virus carrying the mutated PB2 in both avian and mammalian hosts. The MVV mutations caused no weight loss in mice, but they did allow replication in infected lungs, and the viruses acquired fatal mammalian pathogenic mutations such as Q591R/K, E627K, or D701N in the infected lungs. The MVV mutations are located at the interfaces of the trimer and are predicted to increase the strength of this structure. Thus, gaining MVV mutations might be the first step for AIV to acquire mammalian pathogenicity. These results provide new insights into the evolution of AIV in birds and mammals. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=avian%20influenza%20A%20virus" title="avian influenza A virus">avian influenza A virus</a>, <a href="https://publications.waset.org/abstracts/search?q=prototypic%20PB2" title=" prototypic PB2"> prototypic PB2</a>, <a href="https://publications.waset.org/abstracts/search?q=polymerase%20activity" title=" polymerase activity"> polymerase activity</a>, <a href="https://publications.waset.org/abstracts/search?q=mammalian%20pathogenicity" title=" mammalian pathogenicity"> mammalian pathogenicity</a>, <a href="https://publications.waset.org/abstracts/search?q=first-step%20mutations" title=" first-step mutations"> first-step mutations</a> </p> <a href="https://publications.waset.org/abstracts/74659/prerequisites-for-the-acquisition-of-mammalian-pathogenicity-by-influenza-a-virus-with-a-prototypic-avian-pb2-gene" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/74659.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">345</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">266</span> Polymerase Chain Reaction Analysis and Random Amplified Polymorphic DNA of Agrobacterium Tumefaciens </h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Abeer%20M.%20Algeblawi">Abeer M. Algeblawi</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Fifteen isolates of Agrobacterium tumefaciens were obtained from crown gall samples collected from six locations (Tripoli, Alzahra, Ain-Zara, Alzawia, Alazezia in Libya) from Grape (Vitis vinifera L.), Pear (Pyrus communis L.), Peach (Prunus persica L.) and Alexandria in Egypt from Guava (Psidium guajava L.) trees, Artichoke (Cynara cardunculus L.) and Sugar beet (Beta vulgaris L.). Total DNA was extracted from the eight isolates as well as the identification of six isolates used into Polymerase Chain Reaction (PCR) analysis and Random Amplified Polymorphic DNA (RAPD) technique were used. High similarity (55.5%) was observed among the eight A. tumefaciens isolates (Agro1, Agro2, Agro3, Agro4, Agro5, Agro6, Agro7, and Agro8). The PCR amplification products were resulting from the use of two specific primers (virD2A-virD2C). Analysis induction six isolates of A. tumefaciens obtained from different hosts. A visible band was specific to A. tumefaciens of (220 bp, 224 bp) and 338 bp produced with total DNA extracted from bacterial cells. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Agrobacterium%20tumefaciens" title="Agrobacterium tumefaciens">Agrobacterium tumefaciens</a>, <a href="https://publications.waset.org/abstracts/search?q=crown%20gall" title=" crown gall"> crown gall</a>, <a href="https://publications.waset.org/abstracts/search?q=identification" title=" identification"> identification</a>, <a href="https://publications.waset.org/abstracts/search?q=molecular%20characterization" title=" molecular characterization"> molecular characterization</a>, <a href="https://publications.waset.org/abstracts/search?q=PCR" title=" PCR"> PCR</a>, <a href="https://publications.waset.org/abstracts/search?q=RAPD" title=" RAPD"> RAPD</a> </p> <a href="https://publications.waset.org/abstracts/113521/polymerase-chain-reaction-analysis-and-random-amplified-polymorphic-dna-of-agrobacterium-tumefaciens" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/113521.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">144</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">265</span> The Predictive Value of Micro Rna 451 on the Outcome of Imatinib Treatment in Chronic Myeloid Leukemia Patients</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Nehal%20Adel%20Khalil">Nehal Adel Khalil</a>, <a href="https://publications.waset.org/abstracts/search?q=Amel%20Foad%20Ketat"> Amel Foad Ketat</a>, <a href="https://publications.waset.org/abstracts/search?q=Fairouz%20Elsayed%20Mohamed%20Ali"> Fairouz Elsayed Mohamed Ali</a>, <a href="https://publications.waset.org/abstracts/search?q=Nahla%20Abdelmoneim%20Hamid"> Nahla Abdelmoneim Hamid</a>, <a href="https://publications.waset.org/abstracts/search?q=Hazem%20Farag%20Manaa"> Hazem Farag Manaa</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Background: Chronic myeloid leukemia (CML) represents 15% of adult leukemias. Imatinib Mesylate (IM) is the gold standard treatment for new cases of CML. Treatment with IM results in improvement of the majority of cases. However, about 25% of cases may develop resistance. Sensitive and specific early predictors of IM resistance in CML patients have not been established to date. Aim: To investigate the value of miR-451 in CML as an early predictor for IM resistance in Egyptian CML patients. Methods: The study employed Real time Polymerase Reaction (qPCR) technique to investigate the leucocytic expression of miR-451 in fifteen newly diagnosed CML patients (group I), fifteen IM responder CML patients (group II), fifteen IM resistant CML patients (group III) and fifteen healthy subjects of matched age and sex as a control group (group IV). The response to IM was defined as < 10% BCR-ABL transcript level after 3 months of therapy. The following parameters were assessed in subjects of all the studied groups: 1- Complete blood count (CBC). 2- Measurement of plasma level of miRNA 451 using real-time Polymerase Chain Reaction (qPCR). 3- Detection of BCR-ABL gene mutation in CML using qPCR. Results: The present study revealed that miR-451 was significantly down-regulated in leucocytes of newly diagnosed CML patients as compared to healthy subjects. IM responder CML patients showed an up-regulation of miR- 451 compared with IM resistant CML patients. Conclusion: According to the data from the present study, it can be concluded that leucocytic miR- 451 expression is a useful additional follow-up marker for the response to IM and a promising prognostic biomarker for CML. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=chronic%20myeloid%20leukemia" title="chronic myeloid leukemia">chronic myeloid leukemia</a>, <a href="https://publications.waset.org/abstracts/search?q=imatinib%20resistance" title=" imatinib resistance"> imatinib resistance</a>, <a href="https://publications.waset.org/abstracts/search?q=microRNA%20451" title=" microRNA 451"> microRNA 451</a>, <a href="https://publications.waset.org/abstracts/search?q=Polymerase%20Chain%20Reaction" title=" Polymerase Chain Reaction"> Polymerase Chain Reaction</a> </p> <a href="https://publications.waset.org/abstracts/23100/the-predictive-value-of-micro-rna-451-on-the-outcome-of-imatinib-treatment-in-chronic-myeloid-leukemia-patients" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/23100.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">294</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">264</span> Negative RT-PCR in a Newborn Infected with Zika Virus: A Case Report</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Vallejo%20Michael">Vallejo Michael</a>, <a href="https://publications.waset.org/abstracts/search?q=Acu%C3%B1a%20Edgar"> Acuña Edgar</a>, <a href="https://publications.waset.org/abstracts/search?q=Roa%20Juan%20David"> Roa Juan David</a>, <a href="https://publications.waset.org/abstracts/search?q=Pe%C3%B1uela%20Rosa"> Peñuela Rosa</a>, <a href="https://publications.waset.org/abstracts/search?q=Parra%20Alejandra"> Parra Alejandra</a>, <a href="https://publications.waset.org/abstracts/search?q=Casallas%20Daniela"> Casallas Daniela</a>, <a href="https://publications.waset.org/abstracts/search?q=Rodriguez%20Sheyla"> Rodriguez Sheyla </a> </p> <p class="card-text"><strong>Abstract:</strong></p> Congenital Zika Virus Syndrome is an entity composed by a variety of birth defects presented in newborns that have been exposed to the Zika Virus during pregnancy. The syndrome characteristic features are severe microcephaly, cerebral tissue abnormalities, ophthalmological abnormalities such as uveitis and chorioretinitis, arthrogryposis, clubfoot deformity and muscular tone abnormalities. The confirmatory test is the Reverse transcription polymerase chain reaction (RT-PCR) associated to the physical findings. Here we present the case of a newborn with microcephaly whose mother presented a confirmed Zika Virus infection during the third trimester of pregnancy, despite of the evident findings and the history of Zika infection the RT-PCR in amniotic and cerebrospinal fluid of the newborn was negative. RT-PCR has demonstrated a low sensibility in samples with low viral loads, reason why, we propose a clinical diagnosis in patients with clinical history of Zika Virus infection during pregnancy accompanied by evident clinical manifestations of the child. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=congenital" title="congenital">congenital</a>, <a href="https://publications.waset.org/abstracts/search?q=Zika%20virus" title=" Zika virus"> Zika virus</a>, <a href="https://publications.waset.org/abstracts/search?q=microcephaly" title=" microcephaly"> microcephaly</a>, <a href="https://publications.waset.org/abstracts/search?q=reverse%20transcriptase%20polymerase%20chain%20reaction" title=" reverse transcriptase polymerase chain reaction"> reverse transcriptase polymerase chain reaction</a> </p> <a href="https://publications.waset.org/abstracts/84563/negative-rt-pcr-in-a-newborn-infected-with-zika-virus-a-case-report" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/84563.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">211</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">263</span> Rationally Designed Dual PARP-HDAC Inhibitor Elicits Striking Anti-leukemic Effects</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Amandeep%20Thakur">Amandeep Thakur</a>, <a href="https://publications.waset.org/abstracts/search?q=Yi-Hsuan%20Chu"> Yi-Hsuan Chu</a>, <a href="https://publications.waset.org/abstracts/search?q=Chun-Hsu%20Pan"> Chun-Hsu Pan</a>, <a href="https://publications.waset.org/abstracts/search?q=Kunal%20Nepali"> Kunal Nepali</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The transfer of ADP-ribose residues onto target substrates from nicotinamide adenine dinucleotide (NAD) (PARylation) is catalyzed by Poly (ADP-ribose) polymerases (PARPs). Amongst the PARP family members, the DNA damage response in cancer is majorly regulated by PARP1 and PARP2. The blockade of DNA repair by PARP inhibitors leads to the progression of DNA single-strand breaks (induced by some triggering factors) to double-strand breaks. Notably, PARP inhibitors are remarkably effective in cancers with defective homologous recombination repair (HRR). In particular, cancer cells with BRCA mutations are responsive to therapy with PARP inhibitors. The aforementioned requirement for PARP inhibitors to be effective confers a narrow activity spectrum to PARP inhibitors, which hinders their clinical applicability. Thus, the quest to expand the application horizons of PARP inhibitors beyond BRCA mutations is the need of the hour. Literature precedents reveal that HDAC inhibition induces BRCAness in cancer cells and can broaden the therapeutic scope of PARP inhibitors. Driven by such disclosures, dual inhibitors targeting both PARP and HDAC enzymes were designed by our research group to extend the efficacy of PARP inhibitors beyond BRCA-mutated cancers to cancers with induced BRCAness. The design strategy involved the installation of Veliparib, an investigational PARP inhibitor, as a surface recognition part in the HDAC inhibitor pharmacophore model. The chemical architecture of veliparib was deemed appropriate as a starting point for the generation of dual inhibitors by virtue of its size and structural flexibility. A validatory docking study was conducted at the outset to predict the binding mode of the designed dual modulatory chemical architectures. Subsequently, the designed chemical architectures were synthesized via a multistep synthetic route and evaluated for antitumor efficacy. Delightfully, one compound manifested impressive anti-leukemic effects (HL-60 cell lines) mediated via dual inhibition of PARP and class I HDACs. The outcome of the western blot analysis revealed that the compound could downregulate the expression levels of PARP1 and PARP2 and the HDAC isoforms (HDAC1, 2, and 3). Also, the dual PARP-HDAC inhibitor upregulated the protein expression of the acetyl histone H3, confirming its abrogation potential for class I HDACs. In addition, the dual modulator could arrest the cell cycle at the G0/G1 phase and induce autophagy. Further, polymer-based nanoformulation of the dual inhibitor was furnished to afford targeted delivery of the dual inhibitor at the cancer site. Transmission electron microscopy (TEM) results indicate that the nanoparticles were monodispersed and spherical. Moreover, the polymeric nanoformulation exhibited an appropriate particle size. Delightfully, pH-sensitive behavior was manifested by the polymeric nanoformulation that led to selective antitumor effects towards the HL-60 cell lines. In light of the magnificent anti-leukemic profile of the identified dual PARP-HDAC inhibitor, in-vivo studies (pharmacokinetics and pharmacodynamics) are currently being conducted. Notably, the optimistic findings of the aforementioned study have spurred our research group to initiate several medicinal chemistry campaigns to create bifunctional small molecule inhibitors addressing PARP as the primary target. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=PARP%20inhibitors" title="PARP inhibitors">PARP inhibitors</a>, <a href="https://publications.waset.org/abstracts/search?q=HDAC%20inhibitors" title=" HDAC inhibitors"> HDAC inhibitors</a>, <a href="https://publications.waset.org/abstracts/search?q=BRCA%20mutations" title=" BRCA mutations"> BRCA mutations</a>, <a href="https://publications.waset.org/abstracts/search?q=leukemia" title=" leukemia"> leukemia</a> </p> <a href="https://publications.waset.org/abstracts/191592/rationally-designed-dual-parp-hdac-inhibitor-elicits-striking-anti-leukemic-effects" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/191592.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">23</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">262</span> Isothermal Solid-Phase Amplification System for Detection of Yersinia pestis</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Olena%20Mayboroda">Olena Mayboroda</a>, <a href="https://publications.waset.org/abstracts/search?q=Angel%20Gonzalez%20Benito"> Angel Gonzalez Benito</a>, <a href="https://publications.waset.org/abstracts/search?q=Jonathan%20Sabate%20Del%20Rio"> Jonathan Sabate Del Rio</a>, <a href="https://publications.waset.org/abstracts/search?q=Marketa%20Svobodova"> Marketa Svobodova</a>, <a href="https://publications.waset.org/abstracts/search?q=Sandra%20Julich"> Sandra Julich</a>, <a href="https://publications.waset.org/abstracts/search?q=Herbert%20Tomaso"> Herbert Tomaso</a>, <a href="https://publications.waset.org/abstracts/search?q=Ciara%20K.%20O%27Sullivan"> Ciara K. O'Sullivan</a>, <a href="https://publications.waset.org/abstracts/search?q=Ioanis%20Katakis"> Ioanis Katakis</a> </p> <p class="card-text"><strong>Abstract:</strong></p> DNA amplification is required for most molecular diagnostic applications but conventional PCR has disadvantages for field testing. Isothermal amplification techniques are being developed to respond to this problem. One of them is the Recombinase Polymerase Amplification (RPA) that operates at isothermal conditions without sacrificing specificity and sensitivity in easy-to-use formats. In this work RPA was used for the optical detection of solid-phase amplification of the potential biowarfare agent Yersinia pestis. Thiolated forward primers were immobilized on the surface of maleimide-activated microtitre plates for the quantitative detection of synthetic and genomic DNA, with elongation occurring only in the presence of the specific template DNA and solution phase reverse primers. Quantitative detection was achieved via the use of biotinylated reverse primers and post-amplification addition of streptavidin-HRP conjugate. The overall time of amplification and detection was less than 1 hour at a constant temperature of 37oC. Single-stranded and double-stranded DNA sequences were detected achieving detection limits of 4.04*10-13 M and 3.14*10-16 M, respectively. The system demonstrated high specificity with negligible responses to non-specific targets. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=recombinase%20polymerase%20amplification" title="recombinase polymerase amplification">recombinase polymerase amplification</a>, <a href="https://publications.waset.org/abstracts/search?q=Yersinia%20pestis" title=" Yersinia pestis"> Yersinia pestis</a>, <a href="https://publications.waset.org/abstracts/search?q=solid-phase%20detection" title=" solid-phase detection"> solid-phase detection</a>, <a href="https://publications.waset.org/abstracts/search?q=ELONA" title=" ELONA"> ELONA</a> </p> <a href="https://publications.waset.org/abstracts/42960/isothermal-solid-phase-amplification-system-for-detection-of-yersinia-pestis" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/42960.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">303</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">261</span> Evolutionary Prediction of the Viral RNA-Dependent RNA Polymerase of Chandipura vesiculovirus and Related Viral Species </h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Maneesh%20Kumar">Maneesh Kumar</a>, <a href="https://publications.waset.org/abstracts/search?q=Roshan%20Kamal%20Topno"> Roshan Kamal Topno</a>, <a href="https://publications.waset.org/abstracts/search?q=Manas%20Ranjan%20Dikhit"> Manas Ranjan Dikhit</a>, <a href="https://publications.waset.org/abstracts/search?q=Vahab%20Ali"> Vahab Ali</a>, <a href="https://publications.waset.org/abstracts/search?q=Ganesh%20Chandra%20Sahoo"> Ganesh Chandra Sahoo</a>, <a href="https://publications.waset.org/abstracts/search?q=Bhawana"> Bhawana</a>, <a href="https://publications.waset.org/abstracts/search?q=Major%20Madhukar"> Major Madhukar</a>, <a href="https://publications.waset.org/abstracts/search?q=Rishikesh%20Kumar"> Rishikesh Kumar</a>, <a href="https://publications.waset.org/abstracts/search?q=Krishna%20Pandey"> Krishna Pandey</a>, <a href="https://publications.waset.org/abstracts/search?q=Pradeep%20Das"> Pradeep Das</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Chandipura vesiculovirus is an emerging (-) ssRNA viral entity belonging to the genus Vesiculovirus of the family Rhabdoviridae, associated with fatal encephalitis in tropical regions. The multi-functionally active viral RNA-dependent RNA polymerase (vRdRp) that has been incorporated with conserved amino acid residues in the pathogens, assigned to synthesize distinct viral polypeptides. The lack of proofreading ability of the vRdRp produces many mutated variants. Here, we have performed the evolutionary analysis of 20 viral protein sequences of vRdRp of different strains of Chandipura vesiculovirus along with other viral species from genus Vesiculovirus inferred in MEGA6.06, employing the Neighbour-Joining method. The p-distance algorithmic method has been used to calculate the optimum tree which showed the sum of branch length of about 1.436. The percentage of replicate trees in which the associated taxa are clustered together in the bootstrap test (1000 replicates), is shown next to the branches. No mutation was observed in the Indian strains of Chandipura vesiculovirus. In vRdRp, 1230(His) and 1231(Arg) are actively participated in catalysis and, are found conserved in different strains of Chandipura vesiculovirus. Both amino acid residues were also conserved in the other viral species from genus Vesiculovirus. Many isolates exhibited maximum number of mutations in catalytic regions in strains of Chandipura vesiculovirus at position 26(Ser→Ala), 47 (Ser→Ala), 90(Ser→Tyr), 172(Gly→Ile, Val), 172(Ser→Tyr), 387(Asn→Ser), 1301(Thr→Ala), 1330(Ala→Glu), 2015(Phe→Ser) and 2065(Thr→Val) which make them variants under different tropical conditions from where they evolved. The result clarifies the actual concept of RNA evolution using vRdRp to develop as an evolutionary marker. Although, a limited number of vRdRp protein sequence similarities for Chandipura vesiculovirus and other species. This might endow with possibilities to identify the virulence level during viral multiplication in a host. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Chandipura" title="Chandipura">Chandipura</a>, <a href="https://publications.waset.org/abstracts/search?q=%28-%29%20ssRNA" title=" (-) ssRNA"> (-) ssRNA</a>, <a href="https://publications.waset.org/abstracts/search?q=viral%20RNA-dependent%20RNA%20polymerase" title=" viral RNA-dependent RNA polymerase"> viral RNA-dependent RNA polymerase</a>, <a href="https://publications.waset.org/abstracts/search?q=neighbour-joining%20method" title=" neighbour-joining method"> neighbour-joining method</a>, <a href="https://publications.waset.org/abstracts/search?q=p-distance%20algorithmic" title=" p-distance algorithmic"> p-distance algorithmic</a>, <a href="https://publications.waset.org/abstracts/search?q=evolutionary%20marker" title=" evolutionary marker"> evolutionary marker</a> </p> <a href="https://publications.waset.org/abstracts/99638/evolutionary-prediction-of-the-viral-rna-dependent-rna-polymerase-of-chandipura-vesiculovirus-and-related-viral-species" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/99638.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">197</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">260</span> A Novel Small-Molecule Inhibitor of Influenza a Virus Acts by Suppressing PA Endonuclease Activity of the Viral Polymerase</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Shuafeng%20Yuan">Shuafeng Yuan</a>, <a href="https://publications.waset.org/abstracts/search?q=Bojian%20Zheng"> Bojian Zheng</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The RNA-dependent RNA polymerase of influenza a virus comprises conserved and independently folded subdomains with defined functionalities. The N-terminal domain of the PA subunit (PAN) harbors the endonuclease function so that it can serve as a desired target for drug discovery. To identify a class of anti-influenza inhibitors that impedes PAN endonuclease activity, a screening approach that integrated the fluorescence resonance energy transfer based endonuclease inhibitor assay with the DNA gel-based endonuclease inhibitor assay was conducted, followed by the evaluation of antiviral efficacies and potential cytotoxicity of the primary hits in vitro and in vivo. A small-molecule compound ANA-0 was identified as a potent inhibitor against the replication of multiple subtypes of influenza A virus, including H1N1, H3N2, H5N1, H7N7, H7N9 and H9N2, in cell cultures. Combinational treatment of zanamivir and ANA-0 exerted synergistic anti-influenza effect in vitro. Intranasal administration of ANA-0 protected mice from lethal challenge and reduced lung viral loads in H1N1 virus infected BALB/c mice. Docking analyses predicted ANA-0 bound the endonuclease cavity of PAN by interacting with the metal-binding and catalytic residues. In summary, ANA-0 shows potential to be developed to novel anti-influenza agents. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=anti-influenza" title="anti-influenza">anti-influenza</a>, <a href="https://publications.waset.org/abstracts/search?q=novel%20compound" title=" novel compound"> novel compound</a>, <a href="https://publications.waset.org/abstracts/search?q=inhibition%20of%20endonuclease" title=" inhibition of endonuclease"> inhibition of endonuclease</a>, <a href="https://publications.waset.org/abstracts/search?q=PA" title=" PA"> PA</a> </p> <a href="https://publications.waset.org/abstracts/40347/a-novel-small-molecule-inhibitor-of-influenza-a-virus-acts-by-suppressing-pa-endonuclease-activity-of-the-viral-polymerase" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/40347.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">245</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">259</span> Detection of Arcobacter and Helicobacter pylori Contamination in Organic Vegetables by Cultural and Polymerase Chain Reaction (PCR) Methods</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Miguel%20Garc%C3%ADa-Ferr%C3%BAs">Miguel García-Ferrús</a>, <a href="https://publications.waset.org/abstracts/search?q=Ana%20Gonz%C3%A1lez"> Ana González</a>, <a href="https://publications.waset.org/abstracts/search?q=Mar%C3%ADa%20A.%20Ferr%C3%BAs"> María A. Ferrús</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The most demanded organic foods worldwide are those that are consumed fresh, such as fruits and vegetables. However, there is a knowledge gap about some aspects of organic food microbiological quality and safety. Organic fruits and vegetables are more exposed to pathogenic microorganisms due to surface contact with natural fertilizers such as animal manure, wastes and vermicompost used during farming. It has been suggested that some emergent pathogens, such as Helicobacter pylori or Arcobacter spp., could reach humans through the consumption of raw or minimally processed vegetables. Therefore, the objective of this work was to study the contamination of organic fresh green leafy vegetables by Arcobacter spp. and Helicobacter pylori. For this purpose, a total of 24 vegetable samples, 13 lettuce and 11 spinach were acquired from 10 different ecological supermarkets and greengroceries and analyzed by culture and PCR. Arcobacter spp. was detected in 5 samples (20%) by PCR, 4 spinach and one lettuce. One spinach sample was found to be also positive by culture. For H. pylori, the H. pylori VacA gene-specific band was detected in 12 vegetable samples (50%), 10 lettuces and 2 spinach. Isolation in the selective medium did not yield any positive result, possibly because of low contamination levels together with the presence of the organism in its viable but non-culturable form. Results showed significant levels of H. pylori and Arcobacter contamination in organic vegetables that are generally consumed raw, which seems to confirm that these foods can act as transmission vehicles to humans. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Arcobacter%20sp." title="Arcobacter sp.">Arcobacter sp.</a>, <a href="https://publications.waset.org/abstracts/search?q=Helicobacter%20pylori" title="Helicobacter pylori">Helicobacter pylori</a>, <a href="https://publications.waset.org/abstracts/search?q=Organic%20Vegetables" title="Organic Vegetables">Organic Vegetables</a>, <a href="https://publications.waset.org/abstracts/search?q=Polymerase%20Chain%20Reaction%20%28PCR%29" title="Polymerase Chain Reaction (PCR)">Polymerase Chain Reaction (PCR)</a> </p> <a href="https://publications.waset.org/abstracts/140251/detection-of-arcobacter-and-helicobacter-pylori-contamination-in-organic-vegetables-by-cultural-and-polymerase-chain-reaction-pcr-methods" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/140251.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">164</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">258</span> Histone Deacetylases Inhibitor - Valproic Acid Sensitizes Human Melanoma Cells for alkylating agent and PARP inhibitor</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Ma%C5%82gorzata%20Drzewiecka">Małgorzata Drzewiecka</a>, <a href="https://publications.waset.org/abstracts/search?q=Tomasz%20%C5%9Aliwi%C5%84ski"> Tomasz Śliwiński</a>, <a href="https://publications.waset.org/abstracts/search?q=Maciej%20Radek"> Maciej Radek</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The inhibition of histone deacetyles (HDACs) holds promise as a potential anti-cancer therapy because histone and non-histone protein acetylation is frequently disrupted in cancer, leading to cancer initiation and progression. Additionally, histone deacetylase inhibitors (HDACi) such as class I HDAC inhibitor - valproic acid (VPA) have been shown to enhance the effectiveness of DNA-damaging factors, such as cisplatin or radiation. In this study, we found that, using of VPA in combination with talazoparib (BMN-637 – PARP1 inhibitor – PARPi) and/or Dacarabazine (DTIC - alkylating agent) resulted in increased DNA double strand break (DSB) and reduced survival (while not affecting primary melanocytes )and proliferation of melanoma cells. Furthermore, pharmacologic inhibition of class I HDACs sensitizes melanoma cells to apoptosis following exposure to DTIC and BMN-637. In addition, inhibition of HDAC caused sensitization of melanoma cells to dacarbazine and BMN-637 in melanoma xenografts in vivo. At the mRNA and protein level histone deacetylase inhibitor downregulated RAD51 and FANCD2. This study provides that combining HDACi, alkylating agent and PARPi could potentially enhance the treatment of melanoma, which is known for being one of the most aggressive malignant tumors. The findings presented here point to a scenario in which HDAC via enhancing the HR-dependent repair of DSBs created during the processing of DNA lesions, are essential nodes in the resistance of malignant melanoma cells to methylating agent-based therapies. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=melanoma" title="melanoma">melanoma</a>, <a href="https://publications.waset.org/abstracts/search?q=hdac" title=" hdac"> hdac</a>, <a href="https://publications.waset.org/abstracts/search?q=parp%20inhibitor" title=" parp inhibitor"> parp inhibitor</a>, <a href="https://publications.waset.org/abstracts/search?q=valproic%20acid" title=" valproic acid"> valproic acid</a> </p> <a href="https://publications.waset.org/abstracts/167232/histone-deacetylases-inhibitor-valproic-acid-sensitizes-human-melanoma-cells-for-alkylating-agent-and-parp-inhibitor" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/167232.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">82</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">257</span> Detection and Dissemination of Putative Virulence Genes from Brucella Species Isolated from Livestock in Eastern Cape Province of South Africa</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Rudzani%20Manafe">Rudzani Manafe</a>, <a href="https://publications.waset.org/abstracts/search?q=Ezekiel%20Green"> Ezekiel Green </a> </p> <p class="card-text"><strong>Abstract:</strong></p> Brucella, has many different virulence factors that act as a causative agent of brucellosis, depending on the environment and other factors, some factors may play a role more than others during infection and as a result, play a role in becoming a causative agent for pathogenesis. Brucella melitensis and Brucella abortus are considered to be pathogenic to humans. The genetic regularity of nine potential causes of virulence of two Brucella species in Eastern Cape livestock have been examined. A hundred and twenty isolates obtained from Molecular Pathogenesis and Molecular Epidemiology Research Group (MPMERG) were used for this study. All isolates were grown on Brucella agar medium. Nine primer pairs were used for the detection of virB2, virB5, vceC, btpA, btpB, prpA, betB, bpe275, and bspB virulence factors using Polymerase chain reaction (PCR). Approximately 100% was observed for genes BecC and BetB from B. arbotus. While the lowest gene observed was PrpA at 4.6% from B. arbotus. BetB was detected in 34.7%, while virB2 and prpA (0%) were not detected in B. melitensis. The results from this research suggest that most isolates of Brucella have virulence-related genes associated with disease pathogenesis. Finally, our findings showed that Brucella strains in the Eastern Cape Province are extremely virulent as virulence characteristics exist in most strains investigated. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=putative%20virulence%20genes" title="putative virulence genes">putative virulence genes</a>, <a href="https://publications.waset.org/abstracts/search?q=brucella" title=" brucella"> brucella</a>, <a href="https://publications.waset.org/abstracts/search?q=polymerase%20chain%20reaction" title=" polymerase chain reaction"> polymerase chain reaction</a>, <a href="https://publications.waset.org/abstracts/search?q=milk" title=" milk"> milk</a> </p> <a href="https://publications.waset.org/abstracts/129066/detection-and-dissemination-of-putative-virulence-genes-from-brucella-species-isolated-from-livestock-in-eastern-cape-province-of-south-africa" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/129066.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">139</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">256</span> Using Polymerase Chain Reaction Technique to Observe the Resistant Strains of Pectinophora gossypiella against Cry1Ac Expressing Cotton</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Zunnu%20Raen%20Akhtar">Zunnu Raen Akhtar</a>, <a href="https://publications.waset.org/abstracts/search?q=U.%20Irshad"> U. Irshad</a>, <a href="https://publications.waset.org/abstracts/search?q=M.%20Majid"> M. Majid</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Due to the widespread cultivation of transgenic cotton, intense selection pressure resulted in resistant allele in pink bollworm, Pectinophora gossypiella (Gelechiidae: Lepidoptera). A resistant strain of pink bollworm against transgenic cotton has become a challenge to Integrated Resistance Management (IRM) in the World. Laboratory and field studies were conducted to determine the resistant strains of pink bollworm by performing bioassay, extracting the DNA, conducting PCR of both laboratory as well as field collected pink bollworms to observe the developed resistance. In all of the studies, two Bt varieties FH-142 and FH-118 expressing Cry1Ac compared to non-Bt (Control) were tested against pink bollworm. In the laboratory, bioassay results showed that there was no significant mortality difference between Bt and non-Bt varieties. Similar mortality percentage was observed in transgenic and non-transgenic (control) variety. Insects which were survived after bioassay, as well as those collected from the Bt cotton fields, were selected for further molecular studies. DNA extraction followed by PCR was conducted to check the resistant strains in pink bollworm. In field studies, we also observed the population dynamics of pink boll worms on Bt as compared to non-Bt varieties. Laboratory and field studies confirmed that resistant strains occurs in Pakistani Bt cotton fields. Different strategies should be adopted to combat that serious prevailing resistance issues. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=transgenic%20cotton" title="transgenic cotton">transgenic cotton</a>, <a href="https://publications.waset.org/abstracts/search?q=resistance" title=" resistance"> resistance</a>, <a href="https://publications.waset.org/abstracts/search?q=pectinophora%20gossypiella" title=" pectinophora gossypiella"> pectinophora gossypiella</a>, <a href="https://publications.waset.org/abstracts/search?q=" title=" "> </a>, <a href="https://publications.waset.org/abstracts/search?q=integrated%20resistance%20management%20%28IRM%29" title=" integrated resistance management (IRM)"> integrated resistance management (IRM)</a>, <a href="https://publications.waset.org/abstracts/search?q=polymerase%20chain%20reaction%20%28PCR%29" title=" polymerase chain reaction (PCR)"> polymerase chain reaction (PCR)</a> </p> <a href="https://publications.waset.org/abstracts/74361/using-polymerase-chain-reaction-technique-to-observe-the-resistant-strains-of-pectinophora-gossypiella-against-cry1ac-expressing-cotton" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/74361.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">236</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">255</span> The Prevalence of Blood-Borne Viral Infections among Autopsy Cases in Jordan</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Emad%20Al-Abdallat">Emad Al-Abdallat</a>, <a href="https://publications.waset.org/abstracts/search?q=Faris%20G.%20Bakri"> Faris G. Bakri</a>, <a href="https://publications.waset.org/abstracts/search?q=Azmi%20Mahafza"> Azmi Mahafza</a>, <a href="https://publications.waset.org/abstracts/search?q=Rayyan%20Al%20Ali"> Rayyan Al Ali</a>, <a href="https://publications.waset.org/abstracts/search?q=Nidaa%20Ababneh"> Nidaa Ababneh</a>, <a href="https://publications.waset.org/abstracts/search?q=Ahmed%20Idhair"> Ahmed Idhair </a> </p> <p class="card-text"><strong>Abstract:</strong></p> Background: Morgues are high-risk areas for the spread of infection from the cadavers to the staff during the postmortem examination. Infection can spread from corpses to workers by the airborne route, by direct contact, or from needle and sharp object injuries. Objective: Knowledge about the prevalence of these infections among autopsies is prudent to appreciate any risk of transmission and to further enforce safety measures. Method: A total of 242 autopsies were tested. Age ranged from 3 days to 94 years (median 75.5 years, mean 45.3 (21.9 ± SD)). There were 172 (71%) males. Results: The cause of death was considered natural in 137 (56.6%) cases, accidental in 89 (36.8%), homicidal in 9 (3.7%), suicidal in 4 (1.7%), and unknown in 3 (1.2%). Hepatitis B surface antigen was positive in 5 (2.1%) cases. Hepatitis C virus antibody was detected in 5 (2.1%) cases and the hepatitis C virus polymerase chain reaction was positive in 2 of them (0.8%). HIV antibody was not detected in any of the cases. Conclusions: Autopsies can be associated with exposure to blood borne viruses. Autopsies performed during the study period were tested for hepatitis B surface antigen, hepatitis C virus antibody, and human immunodeficiency virus antibody. Positive tests were subsequently confirmed by polymerase chain reaction. There is low prevalence of infections with these viruses in our autopsy cases. However, the risk of transmission remains a threat. Healthcare workers in the forensic departments should adhere to standard precautions. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=autopsy" title="autopsy">autopsy</a>, <a href="https://publications.waset.org/abstracts/search?q=hepatitis%20B%20virus" title=" hepatitis B virus"> hepatitis B virus</a>, <a href="https://publications.waset.org/abstracts/search?q=hepatitis%20C%20virus" title=" hepatitis C virus"> hepatitis C virus</a>, <a href="https://publications.waset.org/abstracts/search?q=human%20immunodeficiency%20virus" title=" human immunodeficiency virus"> human immunodeficiency virus</a>, <a href="https://publications.waset.org/abstracts/search?q=Jordan" title=" Jordan"> Jordan</a> </p> <a href="https://publications.waset.org/abstracts/52932/the-prevalence-of-blood-borne-viral-infections-among-autopsy-cases-in-jordan" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/52932.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">380</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">254</span> Identification of Babesia ovis Through Polymerase Chain Reaction in Sheep and Goat in District Muzaffargarh, Pakistan</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Muhammad%20SAFDAR">Muhammad SAFDAR</a>, <a href="https://publications.waset.org/abstracts/search?q=Mehmet%20%20Ozaslan"> Mehmet Ozaslan</a>, <a href="https://publications.waset.org/abstracts/search?q=Musarrat%20Abbas%20%20Khan"> Musarrat Abbas Khan</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Babesiosis is a haemoparasitic disease due to the multiplication of protozoan’s parasite, Babesia ovis in the red blood cells of the host, and contributes numerous economical losses, including sheep and goat ruminants. The early identification and successful treatment of Babesia Ovis spp. belong to the key steps of control and health management of livestock resources. The objective of this study was to construct a polymerase chain reaction (PCR) based method for the detection of Babesia spp. in small ruminants and to determine the risk factors involved in the spreading of babesiosis infections. A total of 100 blood samples were collected from 50 sheep and 50 goats along with different areas of Muzaffargarh, Pakistan, from randomly selected herds. Data on the characteristics of sheep and goats were collected through questionnaires. Of 100 blood samples examined, 18 were positive for Babesia ovis upon microscopic studies, whereas 11 were positive for the presence of Babesia spp. by PCR assay. For the recognition of parasitic DNA, a set of 500bp oligonucleotide was designed by PCR amplification with sequence 18S rRNA gene for B. ovis. The prevalence of babesiosis in small ruminant’s sheep and goat detected by PCR was significantly higher in female animals (28%) than male herds (08%). PCR analysis of the reference samples showed that the detection limit of the PCR assay was 0.01%. Taken together, all data indicated that this PCR assay was a simple, fast, specific detection method for Babesia ovis species in small ruminants compared to other available methods. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Babesia%20ovis" title="Babesia ovis">Babesia ovis</a>, <a href="https://publications.waset.org/abstracts/search?q=PCR%20amplification" title=" PCR amplification"> PCR amplification</a>, <a href="https://publications.waset.org/abstracts/search?q=18S%20rRNA" title=" 18S rRNA"> 18S rRNA</a>, <a href="https://publications.waset.org/abstracts/search?q=sheep%20and%20goat" title=" sheep and goat"> sheep and goat</a> </p> <a href="https://publications.waset.org/abstracts/118334/identification-of-babesia-ovis-through-polymerase-chain-reaction-in-sheep-and-goat-in-district-muzaffargarh-pakistan" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/118334.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">127</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">253</span> Molecular Characterization of Dirofilaria repens in Dogs from Karnataka, India</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=D.%20S.%20Malatesh">D. S. Malatesh</a>, <a href="https://publications.waset.org/abstracts/search?q=K.%20J.%20Ananda"> K. J. Ananda</a>, <a href="https://publications.waset.org/abstracts/search?q=C.%20Ansar%20Kamran"> C. Ansar Kamran</a>, <a href="https://publications.waset.org/abstracts/search?q=K.%20Ganesh%20Udupa"> K. Ganesh Udupa</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Dirofilaria repens is a mosquito-borne filarioid nematode of dogs and other carnivores and accidentally affects humans. D. repens is reported in many countries, including India. Subcutaneous dirofilariosis caused by D. repens is a zoonotic disease, widely distributed throughout Europe, Asia, and Africa, with higher prevalence reported in dogs from Sri Lanka (30-60%), Iran (61%) and Italy (21-25%). Dirofilariasis in dogs was diagnosed by detection of microfilariae in blood. Identification of different Dirofilaria species was done by using molecular methods like polymerase chain reaction (PCR). Even though many researchers reported molecular evidence of D. repens across India, to our best knowledge there is no data available on molecular diagnosis of D. repens in dogs and its zoonotic implication in Karnataka state a southern state in India. The aim of the present study was to identify the Dirofilaria species occurring in dogs from Karnataka, India. Out of 310 samples screened for the presence of microfilariae using traditional diagnostic methods, 99 (31.93%) were positive for the presence of microfilariae. Based on the morphometry, the microfilariae were identified as D. repens. For confirmation of species, the samples were subjected to PCR using pan filarial primers (DIDR-F1, DIDR-R1) for amplification of internal transcribed spacer region 2 (ITS2) of the ribosomal DNA. The PCR product of 484 base pairs on agarose gel was indicative of D. repens. Hence, a single PCR reaction using pan filarial primers can be used to differentiate filarial species found in dogs. The present study confirms that dirofilarial species occurring in dogs from Karnataka is D. repens and further sequencing studies are needed for genotypic characterization of D. repens. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Dirofilaria%20repens" title="Dirofilaria repens">Dirofilaria repens</a>, <a href="https://publications.waset.org/abstracts/search?q=molecular%20characterization" title=" molecular characterization"> molecular characterization</a>, <a href="https://publications.waset.org/abstracts/search?q=polymerase%20chain%20reaction" title=" polymerase chain reaction"> polymerase chain reaction</a>, <a href="https://publications.waset.org/abstracts/search?q=Karnataka" title=" Karnataka"> Karnataka</a>, <a href="https://publications.waset.org/abstracts/search?q=India" title=" India"> India</a> </p> <a href="https://publications.waset.org/abstracts/109804/molecular-characterization-of-dirofilaria-repens-in-dogs-from-karnataka-india" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/109804.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">142</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">252</span> HLB Disease Detection in Omani Lime Trees using Hyperspectral Imaging Based Techniques</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Jacintha%20Menezes">Jacintha Menezes</a>, <a href="https://publications.waset.org/abstracts/search?q=Ramalingam%20Dharmalingam"> Ramalingam Dharmalingam</a>, <a href="https://publications.waset.org/abstracts/search?q=Palaiahnakote%20Shivakumara"> Palaiahnakote Shivakumara</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In the recent years, Omani acid lime cultivation and production has been affected by Citrus greening or Huanglongbing (HLB) disease. HLB disease is one of the most destructive diseases for citrus, with no remedies or countermeasures to stop the disease. Currently used Polymerase chain reaction (PCR) and enzyme-linked immunosorbent assay (ELISA) HLB detection tests require lengthy and labor-intensive laboratory procedures. Furthermore, the equipment and staff needed to carry out the laboratory procedures are frequently specialized hence making them a less optimal solution for the detection of the disease. The current research uses hyperspectral imaging technology for automatic detection of citrus trees with HLB disease. Omani citrus tree leaf images were captured through portable Specim IQ hyperspectral camera. The research considered healthy, nutrition deficient, and HLB infected leaf samples based on the Polymerase chain reaction (PCR) test. The highresolution image samples were sliced to into sub cubes. The sub cubes were further processed to obtain RGB images with spatial features. Similarly, RGB spectral slices were obtained through a moving window on the wavelength. The resized spectral-Spatial RGB images were given to Convolution Neural Networks for deep features extraction. The current research was able to classify a given sample to the appropriate class with 92.86% accuracy indicating the effectiveness of the proposed techniques. The significant bands with a difference in three types of leaves are found to be 560nm, 678nm, 726 nm and 750nm. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=huanglongbing%20%28HLB%29" title="huanglongbing (HLB)">huanglongbing (HLB)</a>, <a href="https://publications.waset.org/abstracts/search?q=hyperspectral%20imaging%20%28HSI%29" title=" hyperspectral imaging (HSI)"> hyperspectral imaging (HSI)</a>, <a href="https://publications.waset.org/abstracts/search?q=%C2%B7%20omani%20citrus" title=" · omani citrus"> · omani citrus</a>, <a href="https://publications.waset.org/abstracts/search?q=CNN" title=" CNN"> CNN</a> </p> <a href="https://publications.waset.org/abstracts/171237/hlb-disease-detection-in-omani-lime-trees-using-hyperspectral-imaging-based-techniques" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/171237.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">80</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">251</span> Identifying Pathogenic Mycobacterium Species Using Multiple Gene Phylogenetic Analysis</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Lemar%20Blake">Lemar Blake</a>, <a href="https://publications.waset.org/abstracts/search?q=Chris%20Oura"> Chris Oura</a>, <a href="https://publications.waset.org/abstracts/search?q=Ayanna%20C.%20N.%20Phillips%20Savage"> Ayanna C. N. Phillips Savage</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Improved DNA sequencing technology has greatly enhanced bacterial identification, especially for organisms that are difficult to culture. Mycobacteriosis with consistent hyphema, bilateral exophthalmia, open mouth gape and ocular lesions, were observed in various fish populations at the School of Veterinary Medicine, Aquaculture/Aquatic Animal Health Unit. Objective: To identify the species of Mycobacterium that is affecting aquarium fish at the School of Veterinary Medicine, Aquaculture/Aquatic Animal Health Unit. Method: A total of 13 fish samples were collected and analyzed via: Ziehl-Neelsen, conventional polymerase chain reaction (PCR) and real-time PCR. These tests were carried out simultaneously for confirmation. The following combination of conventional primers: 16s rRNA (564 bp), rpoB (396 bp), sod (408 bp) were used. Concatenation of the gene fragments was carried out to phylogenetically classify the organism. Results: Acid fast non-branching bacilli were detected in all samples from homogenized internal organs. All 13 acid fast samples were positive for Mycobacterium via real-time PCR. Partial gene sequences using all three primer sets were obtained from two samples and demonstrated a novel strain. A strain 99% related to Mycobacterium marinum was also confirmed in one sample, using 16srRNA and rpoB genes. The two novel strains were clustered with the rapid growers and strains that are known to affect humans. Conclusions: Phylogenetic analysis demonstrated two novel Mycobacterium strains with the potential of being zoonotic and one strain 99% related to Mycobacterium marinum. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=polymerase%20chain%20reaction" title="polymerase chain reaction">polymerase chain reaction</a>, <a href="https://publications.waset.org/abstracts/search?q=phylogenetic" title=" phylogenetic"> phylogenetic</a>, <a href="https://publications.waset.org/abstracts/search?q=DNA%20sequencing" title=" DNA sequencing"> DNA sequencing</a>, <a href="https://publications.waset.org/abstracts/search?q=zoonotic" title=" zoonotic "> zoonotic </a> </p> <a href="https://publications.waset.org/abstracts/124273/identifying-pathogenic-mycobacterium-species-using-multiple-gene-phylogenetic-analysis" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/124273.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">143</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">250</span> HIV Incidence among Men Who Have Sex with Men Measured by Pooling Polymerase Chain Reaction, and Its Comparison with HIV Incidence Estimated by BED-Capture Enzyme-Linked Immunosorbent Assay and Observed in a Prospective Cohort</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Mei%20Han">Mei Han</a>, <a href="https://publications.waset.org/abstracts/search?q=Jinkou%20Zhao"> Jinkou Zhao</a>, <a href="https://publications.waset.org/abstracts/search?q=Yuan%20Yao"> Yuan Yao</a>, <a href="https://publications.waset.org/abstracts/search?q=Liangui%20Feng"> Liangui Feng</a>, <a href="https://publications.waset.org/abstracts/search?q=Xianbin%20Ding"> Xianbin Ding</a>, <a href="https://publications.waset.org/abstracts/search?q=Guohui%20Wu"> Guohui Wu</a>, <a href="https://publications.waset.org/abstracts/search?q=Chao%20Zhou"> Chao Zhou</a>, <a href="https://publications.waset.org/abstracts/search?q=Lin%20Ouyang"> Lin Ouyang</a>, <a href="https://publications.waset.org/abstracts/search?q=Rongrong%20Lu"> Rongrong Lu</a>, <a href="https://publications.waset.org/abstracts/search?q=Bo%20Zhang"> Bo Zhang </a> </p> <p class="card-text"><strong>Abstract:</strong></p> To compare the HIV incidence estimated using BED capture enzyme linked immunosorbent assay (BED-CEIA) and observed in a cohort against the HIV incidence among men who have sex with men (MSM) measured by pooling polymerase chain reaction (pooling-PCR). A total of 617 MSM subjects were included in a respondent driven sampling survey in Chongqing in 2008. Among the 129 that were tested HIV antibody positive, 102 were defined with long-term infection, 27 were assessed for recent HIV infection (RHI) using BED-CEIA. The remaining 488 HIV negative subjects were enrolled to the prospective cohort and followed-up every 6 months to monitor HIV seroconversion. All of the 488 HIV negative specimens were assessed for acute HIV infection (AHI) using pooling-PCR. Among the 488 negative subjects in the open cohort, 214 (43.9%) were followed-up for six months, with 107 person-years of observation and 14 subjects seroconverted. The observed HIV incidence was 12.5 per 100 person-years (95% CI=9.1-15.7). Among the 488 HIV negative specimens, 5 were identified with acute HIV infection using pooling-PCR at an annual rate of 14.02% (95% CI=1.73-26.30). The estimated HIV-1 incidence was 12.02% (95% CI=7.49-16.56) based on BED-CEIA. The HIV incidence estimated with three different approaches was different among subgroups. In the highly HIV prevalent MSM, it costs US$ 1724 to detect one AHI case, while detection of one case of RHI with BED assay costs only US$ 42. Three approaches generated comparable and high HIV incidences, pooling PCR and prospective cohort are more close to the true level of incidence, while BED-CEIA seemed to be the most convenient and economical approach for at-risk population’s HIV incidence evaluation at the beginning of HIV pandemic. HIV-1 incidences were alarmingly high among MSM population in Chongqing, particularly within the subgroup under 25 years of age and those migrants aged between 25 to 34 years. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=BED-CEIA" title="BED-CEIA">BED-CEIA</a>, <a href="https://publications.waset.org/abstracts/search?q=HIV" title=" HIV"> HIV</a>, <a href="https://publications.waset.org/abstracts/search?q=incidence" title=" incidence"> incidence</a>, <a href="https://publications.waset.org/abstracts/search?q=pooled%20PCR" title=" pooled PCR"> pooled PCR</a>, <a href="https://publications.waset.org/abstracts/search?q=prospective%20cohort" title=" prospective cohort"> prospective cohort</a> </p> <a href="https://publications.waset.org/abstracts/75145/hiv-incidence-among-men-who-have-sex-with-men-measured-by-pooling-polymerase-chain-reaction-and-its-comparison-with-hiv-incidence-estimated-by-bed-capture-enzyme-linked-immunosorbent-assay-and-observed-in-a-prospective-cohort" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/75145.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">411</span> </span> </div> </div> <ul class="pagination"> <li class="page-item disabled"><span class="page-link">&lsaquo;</span></li> <li class="page-item active"><span class="page-link">1</span></li> <li class="page-item"><a class="page-link" href="https://publications.waset.org/abstracts/search?q=poly%28ADP-ribose%29%20polymerase%201%20%28PARP1%29&page=2">2</a></li> <li class="page-item"><a class="page-link" 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