首页> 外文期刊>Journal of proteomics >Comparative proteome analyses of host protein expression in response to Enterovirus 71 and Coxsackievirus A16 infections.
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Comparative proteome analyses of host protein expression in response to Enterovirus 71 and Coxsackievirus A16 infections.

机译:响应肠病毒71和柯萨奇病毒A16感染的宿主蛋白表达的比较蛋白质组分析。

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摘要

Enterovirus 71 (EV71) and Coxsackievirus A16 (CA16) are the main etiological agents of Hand, Foot and Mouth Disease (HFMD), a common disease among children and had caused several outbreaks in the Asia-Pacific region. Although being genetically close to each other, EV71 infection can cause serious and fatal neurological complications like encephalitis, myocarditis, acute flaccid paralysis (AFP) and aseptic meningitis, but not in CA16 infections. In this study, the cellular response of host cells infected with EV71 and CA16 was characterized and compared by 2-dimensional proteome analyses. A total of 16 proteins were identified to be differentially expressed in EV71 and CA16-infected host cells. Desmin and HSP27, both indirectly regulate the contraction of muscle cells, were significantly downregulated as a result of EV71 infection, suggesting a link to acute flaccid paralysis. The ability of EV71 to evade host immune system may be due to the downregulation of MHC-I synthesis proteins like protein disulfide isomerase A3 and calreticulin. Proteins such as nucleophosmin, nuclear ribonucleoprotein C, and eukaryotic translation initiation factor 2 were all downregulated significantly, suggesting the rapid shutting down of host translation machinery by EV71. These findings provide insight into the nature of high virulent EV71 infection as compared to CA16.
机译:肠道病毒71(EV71)和柯萨奇病毒A16(CA16)是手足口病(HFMD)的主要病原体,手足口病是儿童中的常见疾病,并已在亚太地区引起多次暴发。 EV71感染虽然在遗传上彼此接近,但可引起严重且致命的神经系统并发症,例如脑炎,心肌炎,急性弛缓性麻痹(AFP)和无菌性脑膜炎,但在CA16感染中不会。在这项研究中,通过二维蛋白质组分析来表征和比较感染了EV71和CA16的宿主细胞的细胞应答。总共鉴定出16种蛋白质在EV71和CA16感染的宿主细胞中差异表达。 EV71感染可导致Desmin和HSP27都间接调节肌肉细胞的收缩,并被显着下调,表明与急性弛缓性麻痹有关。 EV71逃避宿主免疫系统的能力可能是由于MHC-1合成蛋白(如蛋白二硫键异构酶A3和钙网蛋白)的下调。诸如核磷蛋白,核糖核蛋白C和真核翻译起始因子2之类的蛋白质均被显着下调,这表明EV71可迅速关闭宿主翻译机制。这些发现提供了与CA16相比高毒EV71感染的性质的见解。

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