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传染性鲑鱼贫血病毒(一种鱼类正粘病毒)毒力相关的进化机制。

Evolutionary mechanisms involved in the virulence of infectious salmon anaemia virus (ISAV), a piscine orthomyxovirus.

作者信息

Markussen Turhan, Jonassen Christine Monceyron, Numanovic Sanela, Braaen Stine, Hjortaas Monika, Nilsen Hanne, Mjaaland Siri

机构信息

Department of Food Safety and Infection Biology, Norwegian School of Veterinary Science, P.O. Box 8146 Dep., N-0033 Oslo, Norway.

出版信息

Virology. 2008 May 10;374(2):515-27. doi: 10.1016/j.virol.2008.01.019. Epub 2008 Feb 20.

Abstract

Infectious salmon anaemia virus (ISAV) is an orthomyxovirus causing a multisystemic, emerging disease in Atlantic salmon. Here we present, for the first time, detailed sequence analyses of the full-genome sequence of a presumed avirulent isolate displaying a full-length hemagglutinin-esterase (HE) gene (HPR0), and compare this with full-genome sequences of 11 Norwegian ISAV isolates from clinically diseased fish. These analyses revealed the presence of a virulence marker right upstream of the putative cleavage site R267 in the fusion (F) protein, suggesting a Q266-->L266 substitution to be a prerequisite for virulence. To gain virulence in isolates lacking this substitution, a sequence insertion near the cleavage site seems to be required. This strongly suggests the involvement of a protease recognition pattern at the cleavage site of the fusion protein as a determinant of virulence, as seen in highly pathogenic influenza A virus H5 or H7 and the paramyxovirus Newcastle disease virus.

摘要

传染性鲑鱼贫血病毒(ISAV)是一种正粘病毒,可在大西洋鲑鱼中引发一种多系统的新出现疾病。在此,我们首次展示了一株假定无毒力分离株的全基因组序列的详细序列分析,该分离株具有全长血凝素酯酶(HE)基因(HPR0),并将其与来自临床患病鱼的11株挪威ISAV分离株的全基因组序列进行比较。这些分析揭示,在融合(F)蛋白中假定的裂解位点R267上游存在一个毒力标记,表明Q266→L266的替换是毒力的先决条件。对于缺乏这种替换的分离株,要获得毒力似乎需要在裂解位点附近进行序列插入。这有力地表明,融合蛋白裂解位点处的蛋白酶识别模式参与其中,作为毒力的一个决定因素,这在高致病性甲型流感病毒H5或H7以及副粘病毒新城疫病毒中可见。

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