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首页> 外文期刊>Journal of Virological Methods >A multiplex real-time PCR assay for the detection and differentiation of the newly emerged porcine circovirus type 3 and continuously evolving type 2 strains in the United States
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A multiplex real-time PCR assay for the detection and differentiation of the newly emerged porcine circovirus type 3 and continuously evolving type 2 strains in the United States

机译:用于检测和分化新出现的猪循环系统病毒3型的多重实时PCR测定,并在美国连续发展2型菌株

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摘要

A multiplex quantitative real-time polymerase chain reaction (mqPCR) assay was developed and validated for the detection and differentiation of porcine circovirus type 3 (PCV3) and type 2 (PCV2) strains. The assay coverage was 97.9% (184/188) for PCV3 and 99.1% (1889/1907) for PCV2 sequences that were available from the current GenBank database. The PCR amplification efficiencies were 98-99% for plasmids, and 92-96% for diagnostic samples, with correlation coefficients all greater than 0.99. The limit of detection (LOD) determined as plasmid copies per reaction was 17 for PCV3 and 14 for PCV2. The assay specifically detected the targeted viruses without cross reacting to each other or to other common porcine viruses. Among 336 swine clinical samples collected in 2018, 101 (30.1%) were PCV3 positive, 56 (16.7%) were PCV2 positive and 18 (5.4%) were co-positives. Sixty selected PCV3 positives were confirmed by Sanger sequencing, and 53 of the 56 PCV2 positive samples were tested positive by another validated PCR assay.
机译:多重定量实时聚合酶链反应(MQPCR)测定并验证,用于猪胃肠病毒3(PCV3)和型(PCV2)菌株的检测和分化。对于PCV3和99.1%(1889/1907)的PCV2序列,测定覆盖率为97.9%(184/188),用于从当前的Genbank数据库获得的PCV2序列。质粒的PCR扩增效率为98-99%,诊断样品92-96%,相关系数均大于0.99。测定为每次反应质粒拷贝的检测极限为PCV3和14的PCV2为17。该测定特异性地检测到靶向病毒而不交叉反应彼此或其他常见的猪病毒。在2018年收集的336个猪临床样品中,101个(30.1%)是pcv3阳性,56(16.7%)pcv2阳性,18(5.4%)是共阳性的。通过Sanger测序确认六十选择的PCV3阳性,并且通过另一验证的PCR测定测试56pcv2阳性样品中的53个阳性样品。

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