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[肠道病毒71型或柯萨奇病毒A16感染诱导的正常人呼吸道上皮细胞中Ⅰ型干扰素产生途径相关基因的表达]

[Expression of Type-Ι Interferon Production Pathway-Related Genes Induced by Infection Due to Enterovirus 71 or Coxsackievirus A16 in Normal Human Airway Epithelial Cells].

作者信息

Song Jie, Hu Yajie, Li Jiaqi, Wang Jingjing, Guo Lei, Zheng Huiwen, Ning Ruotong, Wang Lichun, Li Qihan, Liu Longding

出版信息

Bing Du Xue Bao. 2016 Nov;32(6):694-701.

Abstract

Hand, foot, and mouth disease(HFMD)is caused by mainly enterovirus 71(EV-A71)and coxsackievirus A16(CV-A16),and is a serious healthcare problem worldwide.EV-A71 infection is thought to progress readily to serious complications whereas CV-A16 infection, in general, results in mild symptoms and presents repeatedly. However, the underlying mechanisms leading to these differences are not known. We compared changes in expression of type-I interferon(IFN-I)-related genes in normal human bronchial epithelial(16HBE) cells. Gene-expression levels of TLR3,MAVS,MDA5,MyD88,IRF7,IFNαand IFNβwere elevated significantly after EVA71 infection.MDA5expression was increased markedly, and that of TLR3 and IRF3was decreased obviously after CV-A16 infection, but that of MAVS,MyD88,IFNαand IFNβdid not show significant differences. Viral copy number and viral titers suggested that CV-A16 replicates more efficiently than EV-A71 in 16HBE.These results suggest that IFN-I production pathway-related genes in response to infection by EV-A71 and CV-A16 have notable discrepancies. Such information could shine a light on the different manifestations caused by EV-A71 and CV-A16,and the mechanism of repeat infection by CV-A16.

摘要

手足口病(HFMD)主要由肠道病毒71型(EV - A71)和柯萨奇病毒A16型(CV - A16)引起,是一个全球性的严重医疗问题。EV - A71感染易发展为严重并发症,而CV - A16感染通常导致轻微症状且会反复出现。然而,导致这些差异的潜在机制尚不清楚。我们比较了正常人支气管上皮(16HBE)细胞中I型干扰素(IFN - I)相关基因表达的变化。EV - A71感染后,TLR3、MAVS、MDA5、MyD88、IRF7、IFNα和IFNβ的基因表达水平显著升高。CV - A16感染后,MDA5表达明显增加,TLR3和IRF3表达明显降低,但MAVS、MyD88、IFNα和IFNβ表达无显著差异。病毒拷贝数和病毒滴度表明,CV - A16在16HBE细胞中的复制效率高于EV - A71。这些结果表明,EV - A71和CV - A16感染后,IFN - I产生途径相关基因存在显著差异。这些信息可能有助于揭示EV - A71和CV - A16引起的不同临床表现以及CV - A16重复感染的机制。

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