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

被引:77
作者
Lee, CW
Swayne, DE
Linares, JA
Senne, DA
Suarez, DL
机构
[1] USDA ARS, SE Poultry Res Lab, Athens, GA 30605 USA
[2] Texas Vet Med Diagnost Labs, Poultry Diagnost Lab, Gonzales, TX 78629 USA
[3] USDA, Anim & Plant Hlth Inspect Serv, Natl Vet Serv Lab, Ames, IA 50010 USA
关键词
D O I
10.1128/JVI.79.17.11412-11421.2005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In early 2004, an H5N2 avian influenza virus (AM 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.
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页码:11412 / 11421
页数:10
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