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通过聚合酶链反应对加拿大丙型肝炎病毒分离株进行基因分型。

Genotyping of Canadian hepatitis C virus isolates by PCR.

作者信息

Andonov A, Chaudhary R K

机构信息

Laboratory for Viral Hepatitis, Bureau of Microbiology, Health Canada, Ottawa, Ontario.

出版信息

J Clin Microbiol. 1994 Aug;32(8):2031-4. doi: 10.1128/jcm.32.8.2031-2034.1994.

Abstract

We used PCR for hepatitis C virus (HCV) genotyping with type-specific primers from the core and NS5 genes. Type I was predominant in the general population (58% in blood donors) as well as in different risk groups, such as intravenous drug abusers (58%), blood transfusion recipients (64%), hemophiliacs (62%), and patients with HCV chronic liver disease (76%). Types II, III, and IV were less prevalent in Canada, being found in 10.92, 6.72, and 5.88% of the population, respectively. The type II core primer was not type specific and reacted with the majority of our type I HCV samples, suggesting a false-positive dual infection with two different genotypes (I and II). Digestion of these amplified type I and type II products with restriction endonuclease AccI proved to be very useful in the exclusion of false-positive dual type I and type II infections.

摘要

我们使用来自核心基因和NS5基因的型特异性引物,通过聚合酶链反应(PCR)对丙型肝炎病毒(HCV)进行基因分型。I型在普通人群(献血者中占58%)以及不同风险群体中占主导地位,如静脉注射吸毒者(58%)、输血接受者(64%)、血友病患者(62%)和HCV慢性肝病患者(76%)。II型、III型和IV型在加拿大的流行率较低,分别占人群的10.92%、6.72%和5.88%。II型核心引物不具有型特异性,与我们大多数I型HCV样本发生反应,提示存在两种不同基因型(I型和II型)的假阳性双重感染。用限制性内切酶AccI消化这些扩增的I型和II型产物,在排除I型和II型假阳性双重感染方面被证明非常有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44dd/263927/c22af0f19f0a/jcm00008-0211-a.jpg

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