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分析感染 2009(H1N1)和经典猪 H1N1 流感病毒的猪肺泡巨噬细胞细胞蛋白质组变化。

Analysis of cellular proteome alterations in porcine alveolar macrophage cells infected with 2009 (H1N1) and classical swine H1N1 influenza viruses.

机构信息

State Key Laboratory of Agriculture Microbiology, Huazhong Agriculture University, Wuhan 430070, PR China.

出版信息

J Proteomics. 2012 Mar 16;75(6):1732-41. doi: 10.1016/j.jprot.2011.12.012. Epub 2011 Dec 20.

DOI:10.1016/j.jprot.2011.12.012
PMID:22202185
Abstract

The H1N1/2009 influenza virus has the potential to cause a human pandemic, and sporadic cases of human-to-pig transmission have been reported. In this study, two influenza viruses were isolated from pigs. A phylogenetic analysis showed that the A/swine/NanChang/F9/2010(H1N1) (F9/10) strain shared a high degree of homology with the pandemic H1N1/2009 virus, and A/swine/GuangDong/34/2006 (H1N1) (34/06) strains was a classical swine influenza virus. A proteomic analysis was performed to investigate possible alterations of protein expression in porcine alveolar macrophage (PAM) cells infected by the F9/10 and 34/06 viruses over different time courses. Using 2-DE in association with MALDI-TOF MS/MS, we identified 13 up-regulated and 21 down-regulated protein spots, including cytoskeleton proteins, cellular signal transduction proteins, molecular biosynthesis proteins and heat shock proteins. The most significant changes in the infected cells were associated with molecular biosynthesis proteins and heat shock proteins. We analysed the biological characteristics of the F9/10 and 34/06 viruses in vivo and in vitro. The F9/10 virus showed greater pathogenicity than the 34/06 virus in PAM cells and mice. This study provides insights into the biologic characteristics, potential virulence alteration and cross-species transmission mechanisms of the pandemic H1N1/2009.

摘要

从猪分离的两种流感病毒及其对猪肺泡巨噬细胞蛋白表达的影响

甲型 H1N1/2009 流感病毒具有引发人流感大流行的潜力,并且已经有猪传人的散发病例报道。本研究从猪体中分离到了两种流感病毒。系统进化分析表明,A/swine/NanChang/F9/2010(H1N1) (F9/10) 株与大流行的甲型 H1N1/2009 病毒具有高度同源性,而 A/swine/GuangDong/34/2006 (H1N1) (34/06) 株为经典的猪流感病毒。采用蛋白质组学方法,分析了甲型 H1N1/2009 病毒(F9/10 株)和经典的猪流感病毒(34/06 株)感染猪肺泡巨噬细胞(PAM)后不同时间点细胞蛋白表达的变化。应用双向电泳-基质辅助激光解吸电离飞行时间质谱联用技术(2-DE/MALDI-TOF-MS/MS),共鉴定到 13 个上调蛋白点和 21 个下调蛋白点,这些蛋白涉及细胞骨架蛋白、细胞信号转导蛋白、分子生物合成蛋白和热休克蛋白等。感染细胞中发生显著变化的蛋白主要与分子生物合成蛋白和热休克蛋白有关。进一步对 F9/10 株和 34/06 株在体内和体外的生物学特性进行了分析。结果显示,F9/10 株在 PAM 细胞和小鼠体内的致病力强于 34/06 株。本研究为了解大流行的甲型 H1N1/2009 病毒的生物学特性、潜在的毒力改变和跨种传播机制提供了依据。

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