H7N9流感病毒感染A549细胞的蛋白质组学分析

Xiaoman Ding, Ruoxi Yu, Xin Wang, Weihua Wu, Bo Peng, Hui Liu, Yijie Geng, Fangyuan Dong, Jiahai Lu, Muhua Yu, Shisong Fang
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摘要

为探讨H7N9流感病毒的发病机制,建立H7N9流感病毒和H1N1甲型流感病毒(H1N1pdm09)感染A549细胞模型,研究两株感染A549细胞的差异蛋白表达情况。A549细胞感染H7N9和h1n1pdm09流感病毒,感染多重数(MOI)为0.001。采用蛋白质组学方法(2DDIGE联合MALDI-TOF-MS/MS)评估感染后24、48和72小时A549细胞的时间反应(hpi)。分别有11个、12个和33个蛋白在24、48和72hpi时表达显著差异。与H1N1pdm09感染相比,功能分析显示H7N9感染中F-actin-capping蛋白亚基α -1(CapZ-α1)、鸟氨酸转氨酶(OAT)、聚(rC)结合蛋白1(PCBP1)和真核翻译起始因子5A-1(eIF5A)的下调产生了细胞病变作用。血小板活化因子乙酰水解酶eib亚单位β (PAFAH1B2)在H7N9感染中的下调可能与H7N9流感病毒感染患者的临床症状有关。
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[Proteome Profiling of A549 Cells Infected with Influenza H7N9 Virus].

To explore the mechanisms of influenza H7N9 virus pathogenesis, influenza H7N9 virus and H1N1 influenza A virus(H1N1pdm09)-infected A549 cellular models were established, and differential protein expression in A549 cells infected with the two strains were investigated.A549 cells were infected with H7N9 and H1N1pdm09influenza virus at a multiplicity of infection(MOI)of 0.001.The temporal response of A549 cells infected with the two strains was evaluated using the proteomics approaches(2DDIGE combined with MALDI-TOF-MS/MS)at 24,48 and 72hours post infection(hpi).There were 11,12 and 33proteins with significantly different expression at 24,48 and 72hpi,respectively.Compared with H1N1pdm09 infection, functional analysis revealed that the down-regulation of proteins in H7N9 infection including F-actin-capping protein subunit alpha-1(CapZ-α1), ornithine aminotransferase(OAT),poly(rC)-binding protein 1(PCBP1)and eukaryotic translation initiation factor 5A-1(eIF5A)produced cytopathic effects. The down-regulation of platelet-activating factor acetylhydrolaseIb subunit beta(PAFAH1B2)in H7N9-infection may be related to the clinical symptoms of patients infected by the influenza H7N9 virus.

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