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2004年德克萨斯州H5N2禽流感疫情:是美国20年来首例高致病性毒株吗?

H5N2 avian influenza outbreak in Texas in 2004: the first highly pathogenic strain in the United States in 20 years?

作者信息

Lee Chang-Won, Swayne David E, Linares Jose A, Senne Dennis A, Suarez David L

机构信息

Southeast Poultry Research Laboratory, USDA-ARS, Athens, GA 30605, USA.

出版信息

J Virol. 2005 Sep;79(17):11412-21. doi: 10.1128/JVI.79.17.11412-11421.2005.

DOI:10.1128/JVI.79.17.11412-11421.2005
PMID:16103192
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1193578/
Abstract

In early 2004, an H5N2 avian influenza virus (AIV) that met the molecular criteria for classification as a highly pathogenic AIV was isolated from chickens in the state of Texas in the United States. However, clinical manifestations in the affected flock were consistent with avian influenza caused by a low-pathogenicity AIV and the representative virus (A/chicken/Texas/298313/04 [TX/04]) was not virulent for experimentally inoculated chickens. The hemagglutinin (HA) gene of the TX/04 isolate was similar in sequence to A/chicken/Texas/167280-4/02 (TX/02), a low-pathogenicity AIV isolate recovered from chickens in Texas in 2002. However, the TX/04 isolate had one additional basic amino acid at the HA cleavage site, which could be attributed to a single point mutation. The TX/04 isolate was similar in sequence to TX/02 isolate in several internal genes (NP, M, and NS), but some genes (PA, PB1, and PB2) had sequence of a clearly different origin. The TX/04 isolate also had a stalk deletion in the NA gene, characteristic of a chicken-adapted AIV. By analyzing viruses constructed by in vitro mutagenesis followed by reverse genetics, we found that the pathogenicity of the TX/04 virus could be increased in vitro and in vivo by the insertion of an additional basic amino acid at the HA cleavage site and not by the loss of a glycosylation site near the cleavage site. Our study provides the genetic and biologic characteristics of the TX/04 isolate, which highlight the complexity of the polygenic nature of the virulence of influenza viruses.

摘要

2004年初,从美国得克萨斯州的鸡群中分离出一种H5N2禽流感病毒(AIV),该病毒符合高致病性AIV的分子分类标准。然而,受感染鸡群的临床表现与低致病性AIV引起的禽流感一致,并且代表性病毒(A/鸡/得克萨斯/298313/04 [TX/04])对实验接种的鸡没有致病性。TX/04分离株的血凝素(HA)基因序列与2002年从得克萨斯州鸡群中分离出的低致病性AIV分离株A/鸡/得克萨斯/167280 - 4/02(TX/02)相似。然而,TX/04分离株在HA裂解位点多了一个碱性氨基酸,这可能归因于一个单点突变。TX/04分离株在几个内部基因(NP、M和NS)上的序列与TX/02分离株相似,但一些基因(PA、PB1和PB2)具有明显不同来源的序列。TX/04分离株的NA基因也有一个柄部缺失,这是鸡适应型AIV的特征。通过分析体外诱变后再经反向遗传学构建的病毒,我们发现TX/04病毒的致病性可通过在HA裂解位点插入一个额外的碱性氨基酸在体外和体内增强,而不是通过裂解位点附近糖基化位点的缺失。我们的研究提供了TX/04分离株的遗传和生物学特性,突出了流感病毒毒力多基因性质的复杂性。

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