A Novel Capillary Electrophoresis-Based High-Throughput Multiplex Polymerase Chain Reaction System for the Simultaneous Detection of Nine Pathogens in Swine
Here we aimed to develop a capillary electrophoresis-based high-throughput multiplex polymerase chain reaction (PCR) system for the simultaneous detection of nine pathogens in swine. Nine pairs of specific primers and a set of universal primers were designed; the multiplex PCR was established. The s...
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Veröffentlicht in: | BioMed research international 2017-01, Vol.2017 (2017), p.1-8 |
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creator | Tang, Zi-zhong Yang, Ze-xiao Wang, Yin An, Wei Chen, Shi-jie Yang, Miao Lin, Hua Xiao, Lu Wu, Xu-long Yao, Xue-ping |
description | Here we aimed to develop a capillary electrophoresis-based high-throughput multiplex polymerase chain reaction (PCR) system for the simultaneous detection of nine pathogens in swine. Nine pairs of specific primers and a set of universal primers were designed; the multiplex PCR was established. The specificity and cross-reactivity of this assay were examined, and the detection limit was determined using serial 10-fold dilutions of plasmids containing the target sequences. The assay was further tested using 144 clinical samples. We found that the nine specific amplification peaks were observed, and the assay had a high degree of specificity, without nonspecific amplification. The simultaneous detection limit for the nine viruses reached 10000 copies μL−1 when all of the premixed viral targets were present. Seventy-seven of the clinical samples tested positive for at least one of the viruses; the principal viral infections in the clinical samples were porcine circovirus type 2 and porcine reproductive and respiratory syndrome virus. This approach has much potential for further development of high-throughput detection tools for the diagnosis of diseases in animals. |
doi_str_mv | 10.1155/2017/7243909 |
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Nine pairs of specific primers and a set of universal primers were designed; the multiplex PCR was established. The specificity and cross-reactivity of this assay were examined, and the detection limit was determined using serial 10-fold dilutions of plasmids containing the target sequences. The assay was further tested using 144 clinical samples. We found that the nine specific amplification peaks were observed, and the assay had a high degree of specificity, without nonspecific amplification. The simultaneous detection limit for the nine viruses reached 10000 copies μL−1 when all of the premixed viral targets were present. Seventy-seven of the clinical samples tested positive for at least one of the viruses; the principal viral infections in the clinical samples were porcine circovirus type 2 and porcine reproductive and respiratory syndrome virus. This approach has much potential for further development of high-throughput detection tools for the diagnosis of diseases in animals.</description><identifier>ISSN: 2314-6133</identifier><identifier>EISSN: 2314-6141</identifier><identifier>DOI: 10.1155/2017/7243909</identifier><identifier>PMID: 28691030</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Animal behavior ; Animal care ; Animals ; Automation ; Bacteria - isolation & purification ; Capillary electrophoresis ; Colleges & universities ; Cross Reactions ; Deoxyribonucleic acid ; Design ; DNA ; Electrophoresis ; Electrophoresis, Capillary - methods ; Foot & mouth disease ; Health aspects ; Hogs ; Laboratory animals ; Limit of Detection ; Multiplex Polymerase Chain Reaction - methods ; Pathogenic microorganisms ; Pathogens ; Polymerase chain reaction ; Product testing ; Quarantine ; Salmonella ; Sensitivity and Specificity ; Software ; Staphylococcus infections ; Swine ; Testing laboratories ; Viruses ; Viruses - isolation & purification</subject><ispartof>BioMed research international, 2017-01, Vol.2017 (2017), p.1-8</ispartof><rights>Copyright © 2017 Xu-long Wu et al.</rights><rights>COPYRIGHT 2017 John Wiley & Sons, Inc.</rights><rights>Copyright © 2017 Xu-long Wu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright © 2017 Xu-long Wu et al. 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c499t-e525a75dabd199b8b0b875fcd03b5d00a1181ec93c73af72fafb2b3106c579ca3</citedby><cites>FETCH-LOGICAL-c499t-e525a75dabd199b8b0b875fcd03b5d00a1181ec93c73af72fafb2b3106c579ca3</cites><orcidid>0000-0001-7414-5550 ; 0000-0002-1275-8754 ; 0000-0002-2680-5953 ; 0000-0002-0907-7392 ; 0000-0002-2750-9355 ; 0000-0003-3180-9702 ; 0000-0003-2627-829X ; 0000-0001-7229-8326 ; 0000-0001-9470-8170 ; 0000-0002-5801-9375</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485272/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485272/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53770,53772</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28691030$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Zhang, Yanjin</contributor><creatorcontrib>Tang, Zi-zhong</creatorcontrib><creatorcontrib>Yang, Ze-xiao</creatorcontrib><creatorcontrib>Wang, Yin</creatorcontrib><creatorcontrib>An, Wei</creatorcontrib><creatorcontrib>Chen, Shi-jie</creatorcontrib><creatorcontrib>Yang, Miao</creatorcontrib><creatorcontrib>Lin, Hua</creatorcontrib><creatorcontrib>Xiao, Lu</creatorcontrib><creatorcontrib>Wu, Xu-long</creatorcontrib><creatorcontrib>Yao, Xue-ping</creatorcontrib><title>A Novel Capillary Electrophoresis-Based High-Throughput Multiplex Polymerase Chain Reaction System for the Simultaneous Detection of Nine Pathogens in Swine</title><title>BioMed research international</title><addtitle>Biomed Res Int</addtitle><description>Here we aimed to develop a capillary electrophoresis-based high-throughput multiplex polymerase chain reaction (PCR) system for the simultaneous detection of nine pathogens in swine. Nine pairs of specific primers and a set of universal primers were designed; the multiplex PCR was established. The specificity and cross-reactivity of this assay were examined, and the detection limit was determined using serial 10-fold dilutions of plasmids containing the target sequences. The assay was further tested using 144 clinical samples. We found that the nine specific amplification peaks were observed, and the assay had a high degree of specificity, without nonspecific amplification. The simultaneous detection limit for the nine viruses reached 10000 copies μL−1 when all of the premixed viral targets were present. Seventy-seven of the clinical samples tested positive for at least one of the viruses; the principal viral infections in the clinical samples were porcine circovirus type 2 and porcine reproductive and respiratory syndrome virus. This approach has much potential for further development of high-throughput detection tools for the diagnosis of diseases in animals.</description><subject>Animal behavior</subject><subject>Animal care</subject><subject>Animals</subject><subject>Automation</subject><subject>Bacteria - isolation & purification</subject><subject>Capillary electrophoresis</subject><subject>Colleges & universities</subject><subject>Cross Reactions</subject><subject>Deoxyribonucleic acid</subject><subject>Design</subject><subject>DNA</subject><subject>Electrophoresis</subject><subject>Electrophoresis, Capillary - methods</subject><subject>Foot & mouth disease</subject><subject>Health aspects</subject><subject>Hogs</subject><subject>Laboratory animals</subject><subject>Limit of Detection</subject><subject>Multiplex Polymerase Chain Reaction - methods</subject><subject>Pathogenic microorganisms</subject><subject>Pathogens</subject><subject>Polymerase chain reaction</subject><subject>Product testing</subject><subject>Quarantine</subject><subject>Salmonella</subject><subject>Sensitivity and Specificity</subject><subject>Software</subject><subject>Staphylococcus infections</subject><subject>Swine</subject><subject>Testing laboratories</subject><subject>Viruses</subject><subject>Viruses - 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subjects | Animal behavior Animal care Animals Automation Bacteria - isolation & purification Capillary electrophoresis Colleges & universities Cross Reactions Deoxyribonucleic acid Design DNA Electrophoresis Electrophoresis, Capillary - methods Foot & mouth disease Health aspects Hogs Laboratory animals Limit of Detection Multiplex Polymerase Chain Reaction - methods Pathogenic microorganisms Pathogens Polymerase chain reaction Product testing Quarantine Salmonella Sensitivity and Specificity Software Staphylococcus infections Swine Testing laboratories Viruses Viruses - isolation & purification |
title | A Novel Capillary Electrophoresis-Based High-Throughput Multiplex Polymerase Chain Reaction System for the Simultaneous Detection of Nine Pathogens in Swine |
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