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A triplex real-time PCR for differential detection of classical, variant and Bartha-K61 vaccine strains of pseudorabies virus

机译:三重实时荧光定量PCR用于鉴别检测狂犬病病毒的经典,变异和Bartha-K61疫苗株

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Pseudorabies (PR), also known as Aujeszky's disease, is an economically important infectious disease of pigs and other animals caused by pseudorabies virus (PRV). Since late 2011, increasing numbers of PR outbreaks have been reported on many Bartha-K61-vaccinated pig farms in China, and emerging PRV variants that differ from classical PRV strains genetically and antigenically have been confirmed to be responsible for the outbreaks. Accordingly, there is a need to differentiate diverse PRV strains co-circulating in the field. Here, we developed and evaluated a triplex real-time PCR for differential detection of wild-type PRV (classical and variant strains) and gE/gI gene-deleted vaccine strains based on three differently labeled TaqMan probes. The detection limits of the assay were 0.5 TCID50 for classical strains, 0.2 TCID50 for variant strains and 0.05 TCID50 for vaccine strains. The sensitivity was also determined to be 50, 50 and 5 copies for the TJ, SC and Bartha-K61 strain, respectively. The assay did not show cross-reactivity with several common porcine viruses. Reproducibility tests showed that the inter- and intra-assay coefficients of variation were less than 3 %. When testing a total of 234 clinical swine samples, the agreement between the triplex real-time PCR and virus isolation was 100 % (234/234) for classical strains, 99.5 % (233/234) for variant strains, and 100 % (234/234) for the Bartha-K61 vaccine strain. The results demonstrate that this method is sensitive and specific and will be useful for rapid detection and differentiation of diverse PRV strains.
机译:伪狂犬病(PR),也称为Aujeszky病,是由伪狂犬病病毒(PRV)引起的猪和其他动物在经济上重要的传染病。自2011年下半年以来,据报道,中国许多Bartha-K61疫苗接种猪场的PR暴发数量不断增加,并且已证实遗传和抗原性不同于经典PRV株的新兴PRV变异体是造成暴发的原因。因此,需要区分在现场共同循环的各种PRV株。在这里,我们基于三种不同标记的TaqMan探针,开发并评估了用于实时检测野生型PRV(经典和变异株)和gE / gI基因缺失疫苗株的三重实时PCR。该测定的检出限为经典菌株为0.5 TCID50,变异菌株为0.2 TCID50,疫苗菌株为0.05 TCID50。还确定对于TJ,SC和Bartha-K61菌株的敏感性分别为50、50和5个拷贝。该测定未显示与几种常见的猪病毒的交叉反应性。再现性测试表明,批内和批内变异系数小于3%。当总共测试234个临床猪样品时,三重实时荧光定量PCR和病毒分离之间的一致性为经典菌株为100%(234/234),变异株为99.5%(233/234),而100%(234 / 234)用于Bartha-K61疫苗株。结果表明,该方法灵敏,特异,可用于快速检测和区分各种PRV株。

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