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
Hauptverfasser: 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
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container_issue 2017
container_start_page 1
container_title BioMed research international
container_volume 2017
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. 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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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