猫泛白细胞减少症病毒、猫博卡病毒和猫星状病毒多重 PCR 检测方法的建立及应用。

Development and application of a multiplex PCR method for the simultaneous detection and differentiation of feline panleukopenia virus, feline bocavirus, and feline astrovirus.

机构信息

College of Animal Science and Technology, Jilin Agricultural University, Changchun, 130118, Jilin, China.

College of Global Change and Earth System Science, Beijing Normal University, Beijing, 100875, China.

出版信息

Arch Virol. 2019 Nov;164(11):2761-2768. doi: 10.1007/s00705-019-04394-8. Epub 2019 Sep 10.

Abstract

A multiplex polymerase chain reaction (mPCR) assay was developed to detect and distinguish feline panleukopenia virus (FPV), feline bocavirus (FBoV) and feline astrovirus (FeAstV). Three pairs of primers were designed based on conserved regions in the genomic sequences of the three viruses and were used to specifically amplify targeted fragments of 237 bp from the VP2 gene of FPV, 465 bp from the NP1 gene of FBoV and 645 bp from the RdRp gene of FeAstV. The results showed that this mPCR assay was effective, because it could detect at least 2.25-4.04 × 10 copies of genomic DNA of the three viruses per μl, was highly specific, and had a good broad-spectrum ability to detect different genotypes of the targeted viruses. A total of 197 faecal samples that had been screened previously for FeAstV and FBoV were collected from domestic cats in northeast China and were tested for the three viruses using the newly developed mPCR assay. The total positive rate for these three viruses was 59.89% (118/197). From these samples, DNA from FPV, FBoV and FeAstV was detected in 73, 51 and 46 faecal samples, respectively. The mPCR testing results agreed with the routine PCR results with a coincidence rate of 100%. The results of this study show that this mPCR assay can simultaneously detect and differentiate FPV, FBoV and FeAstV and can be used as an easy, specific and efficient detection tool for clinical diagnosis and epidemiological investigation of these three viruses.

摘要

建立了一种多重聚合酶链反应(mPCR)检测方法,用于检测和区分猫泛白细胞减少症病毒(FPV)、猫博卡病毒(FBoV)和猫星状病毒(FeAstV)。根据三种病毒基因组序列的保守区域设计了三对引物,用于特异性扩增 FPV 的 VP2 基因、FBoV 的 NP1 基因和 FeAstV 的 RdRp 基因的目标片段,分别为 237bp、465bp 和 645bp。结果表明,该 mPCR 检测方法有效,因为它可以检测到至少 2.25-4.04×10 拷贝/μl 的三种病毒的基因组 DNA,具有高度特异性,并且具有良好的广谱能力,能够检测到目标病毒的不同基因型。从中国东北地区的家猫中收集了先前筛选出的 FeAstV 和 FBoV 的 197 份粪便样本,使用新开发的 mPCR 检测方法对这三种病毒进行检测。这三种病毒的总阳性率为 59.89%(118/197)。从这些样本中,分别在 73、51 和 46 份粪便样本中检测到了 FPV、FBoV 和 FeAstV 的 DNA。mPCR 检测结果与常规 PCR 结果完全一致,符合率为 100%。本研究结果表明,该 mPCR 检测方法可同时检测和区分 FPV、FBoV 和 FeAstV,可作为临床诊断和三种病毒流行病学调查的简便、特异、高效的检测工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9a0/7086731/8a807880afda/705_2019_4394_Fig1_HTML.jpg

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