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从野鸭中分离出的低致病性 H7N7 禽流感病毒在鸡中致病的因素。

Factors responsible for pathogenicity in chickens of a low-pathogenic H7N7 avian influenza virus isolated from a feral duck.

机构信息

Laboratory of Microbiology, Department of Disease Control, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo, 060-0818, Japan.

出版信息

Arch Virol. 2013 Dec;158(12):2473-8. doi: 10.1007/s00705-013-1762-z. Epub 2013 Jun 19.

DOI:10.1007/s00705-013-1762-z
PMID:23779115
Abstract

Highly pathogenic avian influenza viruses have poly-basic amino acid sequences at the cleavage site in their hemagglutinin (HA). Although this poly-basic region is a prerequisite factor for pathogenicity in chickens, not much is known about additional factors responsible for the acquisition of pathogenicity of the duck influenza virus in chickens. Here, we introduced multiple basic amino acid residues into the HA cleavage site of the A/duck/Hokkaido/Vac-2/2004 (H7N7) strain of avian influenza virus, which has low pathogenicity in chickens; the resultant Vac2sub-P0 strain was not intravenously pathogenic in chickens. In contrast, the Vac2sub-P3 strain, which was recovered from three consecutive passages of Vac2sub-P0 in chicks, was intravenously pathogenic in chickens. Six amino acid substitutions were identified by comparison of the Vac2sub-P3 and Vac2sub-P0 genomic sequences: Lys123Glu in PB2, Asn16Asp in PB1, Glu227Gly and Ile388Thr in HA, Gly228Arg in M1, and Leu46Pro in M2. The results of intravenous inoculations of chickens with recombinant virus indicated that all six amino acid substitutions were required to varying degrees for Vac2sub-P3 pathogenicity, with Glu227Gly and Ile388Thr in HA being particularly essential. These results reveal the roles of additional viral factors in the acquisition of pathogenicity in addition to the previously characterized role of the poly-basic amino acid sequences at the HA cleavage site.

摘要

高致病性禽流感病毒在其血凝素(HA)的裂解位点具有多碱性氨基酸序列。虽然这个多碱性区域是鸡致病性的先决条件因素,但对于鸭流感病毒在鸡中获得致病性的其他因素知之甚少。在这里,我们在 A/鸭/北海道/Vac-2/2004(H7N7)禽流感病毒的 HA 裂解位点引入了多个碱性氨基酸残基,该病毒在鸡中具有低致病性;所得的 Vac2sub-P0 株在鸡中不能静脉内致病。相比之下,从 Vac2sub-P0 在雏鸡中的连续三次传代中回收的 Vac2sub-P3 株在鸡中具有静脉内致病性。通过比较 Vac2sub-P3 和 Vac2sub-P0 基因组序列,鉴定了六个氨基酸取代:PB2 中的 Lys123Glu、PB1 中的 Asn16Asp、HA 中的 Glu227Gly 和 Ile388Thr、M1 中的 Gly228Arg 和 M2 中的 Leu46Pro。用重组病毒对鸡进行静脉接种的结果表明,六个氨基酸取代在不同程度上都需要 Vac2sub-P3 致病性,其中 HA 中的 Glu227Gly 和 Ile388Thr 尤为关键。这些结果揭示了除了先前表征的 HA 裂解位点多碱性氨基酸序列的作用外,病毒因子在获得致病性方面的额外作用。

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