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通过实时逆转录聚合酶链反应快速检测高致病性中国型猪繁殖与呼吸综合征病毒分离株

Rapid detection of a highly virulent Chinese-type isolate of Porcine Reproductive and Respiratory Syndrome Virus by real-time reverse transcriptase PCR.

作者信息

Xiao Xing-Long, Wu Hui, Yu Yi-Gang, Cheng Bang-Zhao, Yang Xiao-Quan, Chen Gu, Liu Dong-Mei, Li Xiao-Feng

机构信息

Institution of Food Safety, Department of Food, College of Light Industry & Food, South China University of Technology, Guangzhou 510640, China.

出版信息

J Virol Methods. 2008 Apr;149(1):49-55. doi: 10.1016/j.jviromet.2008.01.009. Epub 2008 Mar 3.

DOI:10.1016/j.jviromet.2008.01.009
PMID:18313768
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7119963/
Abstract

An outbreak of highly virulent Chinese-type of Porcine Reproductive and Respiratory Syndrome Virus (H-PRRSV) in most areas of China recently has led to huge economic losses and drawn great attention to its diagnosis and disease control. To facilitate rapid identification of H-PRRSV, a fluorogenic-probe hydrolysis (TaqMan)-reverse transcriptase PCR for H-PRRSV has been developed. Primers and probe specificity were evaluated with RNA extracted from 5 strains of H-PRRSV and 24 strains of other viruses, the results showed 100% specificity for the selected panel. The assay met the sensitivity of 1 50% tissue culture infective dose (TCID50) per ml of samples from infected pigs. Analysis with 10(5)-1TCID50/ml H-PRRSV samples demonstrated high reproducibility with a coefficient of variation (CV) of 0.5-2.5%. More than two hundred samples from lung, spleen, blood serum specimens obtained from 22 outbreaks of suspected H-PRRS from March to June in 2007 were verified using this assay. The results showed that 68.5% (146 out of 213) of these samples were positive which is 100% consistent with that of the sequencing method. The assay can be performed in less than 3h and thus provide a rapid method for the diagnosis of H-PRRSV as well as for elucidation of the epidemiology of H-PRRSV infections.

摘要

近期,高致病性中国型猪繁殖与呼吸综合征病毒(H-PRRSV)在中国大部分地区爆发,导致了巨大的经济损失,其诊断和疾病防控也备受关注。为便于快速鉴定H-PRRSV,已开发出一种用于H-PRRSV的荧光探针水解(TaqMan)逆转录PCR方法。用从5株H-PRRSV和24株其他病毒中提取的RNA评估引物和探针的特异性,结果显示对所选病毒组具有100%的特异性。该检测方法对感染猪的样本每毫升达到了1 50%组织培养感染剂量(TCID50)的灵敏度。对10(5)-1TCID50/ml的H-PRRSV样本进行分析,显示出高重复性,变异系数(CV)为0.5-2.5%。使用该检测方法对2007年3月至6月从22起疑似H-PRRS疫情中获取的两百多个肺、脾、血清样本进行了验证。结果显示,这些样本中有68.5%(213个样本中的146个)呈阳性,这与测序方法的结果100%一致。该检测方法可在不到3小时内完成,从而为H-PRRSV的诊断以及H-PRRSV感染的流行病学研究提供了一种快速方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77b3/7119963/2141f798ad8f/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77b3/7119963/9795945b97c6/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77b3/7119963/6f1b7c21b857/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77b3/7119963/91cb9feb30ca/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77b3/7119963/2141f798ad8f/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77b3/7119963/9795945b97c6/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77b3/7119963/6f1b7c21b857/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77b3/7119963/91cb9feb30ca/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77b3/7119963/2141f798ad8f/gr4.jpg

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