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用于检测犬冠状病毒的巢式聚合酶链反应检测方法的开发。

Development of a nested PCR assay for the detection of canine coronavirus.

作者信息

Pratelli A, Tempesta M, Greco G, Martella V, Buonavoglia C

机构信息

Department of Health and Animal Welfare, Faculty of Veterinary Medicine, University of Bari, Valenzano, Italy.

出版信息

J Virol Methods. 1999 Jun;80(1):11-5. doi: 10.1016/s0166-0934(99)00017-8.

Abstract

A diagnostic test for canine coronavirus (CCV) infection based on a nested polymerase chain reaction (n-PCR) assay was developed and tested using the following coronavirus strains: CCV (USDA strain), CCV (45/93, field strain), feline infectious peritonitis virus (FIPV, field strain), transmissible gastroenteritis virus (TGEV, Purdue strain), bovine coronavirus (BCV, 9WBL-77 strain), infectious bronchitis virus (IBV, M-41 strain) and fecal samples of dogs with CCV enteritis. A 230-bp segment of the gene encoding for transmembrane protein M of CCV is the target sequence of the primer. The test described in the present study was able to amplify both CCV and TGEV strains and also gave positive results on fecal samples from CCV infected dogs. n-PCR has a sensitivity as high as isolation on cell cultures, and can therefore be used for the diagnosis of CCV infection in dogs.

摘要

基于巢式聚合酶链反应(n-PCR)分析开发了一种用于犬冠状病毒(CCV)感染的诊断测试,并使用以下冠状病毒株进行了测试:CCV(美国农业部株)、CCV(45/93,野外株)、猫传染性腹膜炎病毒(FIPV,野外株)、传染性胃肠炎病毒(TGEV,普渡株)、牛冠状病毒(BCV,9WBL - 77株)、传染性支气管炎病毒(IBV,M - 41株)以及患有CCV肠炎的犬的粪便样本。编码CCV跨膜蛋白M的基因的230bp片段是引物的靶序列。本研究中描述的测试能够扩增CCV和TGEV株,并且对来自CCV感染犬的粪便样本也给出了阳性结果。n-PCR具有与细胞培养分离一样高的灵敏度,因此可用于犬CCV感染的诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c41d/7119595/090747b2da23/gr1.jpg

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