首页> 外文期刊>Virus Research: An International Journal of Molecular and Cellular Virology >Comparison analysis of microRNAs in response to dengue virus type 2 infection between the Vero cell-adapted strain and its source, the clinical C6/36 isolated strain
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Comparison analysis of microRNAs in response to dengue virus type 2 infection between the Vero cell-adapted strain and its source, the clinical C6/36 isolated strain

机译:微小RNA响应登革热病毒2型感染的临床病毒适应菌株及其来源的比较分析,临床C6 / 36分离株

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摘要

To elucidate the differences in microRNAs during dengue virus infection between Vero cell adapted strain (DENV-2-Vero) and its source, the clinical C6/36 isolated strain (DENV-2-C6/36), a comparison analysis was performed in Vero cells by high throughput sequencing. The results showed that the expression of 16 known and 3 novel miRNAs exhibited marked differences. 5 known miRNAs were up-regulated in DENV-2-C6/36 group, while 11 known microRNAs were down-regulated in DENV-2-Vero group. The GO enrichment and KEGG pathway analysis showed that there was a distinct difference in regulating viral replication between two strains. In DENV-2-Vero infection group, significantly enriched GO terms included virion attachment to host cells, viral structural protein/genome processing and packaging. Meanwhile, the regulation of cell death and apoptosis between two groups were different in the early stage of infection. KEGG enrichment analysis showed that DENV-2-C6/36 infection induced more intense regulation of immune-related pathways, including Fc gamma R-mediated phagocytosis, etc. DENV-2-Vero infection could partially alleviate the immune defense of Vero cells compared with DENV-2-C6/36. The results indicated that the distinct microRNA changes induced by two DENV-2 strains may be partly related to their infective abilities. Our data provide useful insights that help elucidate the host-pathogen interactions following DENV infection.
机译:为了阐明Vero细胞适应菌株(Denv-2-Vero)与其来源之间登革热病毒感染期间MicroRNA的差异,临床C6 / 36分离菌株(Denv-2-C6 / 36),在VERO中进行了比较分析通过高通量测序的细胞。结果表明,已知的16种和3个新的MiRNA表达表现出明显的差异。 5名已知的miRNA在DenV-2-C6 / 36组中调节,而11个已知的MicroRNA在DenV-2-Vero组中下调。 GO富集和KEGG途径分析表明,在两个菌株之间调节病毒复制存在明显差异。在Denv-2-Vero感染组中,显着富集的GO术语包括宿主细胞的病毒素附着,病毒结构蛋白/基因组加工和包装。同时,感染早期的两组细胞死亡和细胞凋亡的调节不同。 KEGG浓缩分析显示DENV-2-C6 / 36感染诱导免疫相关途径的更强烈调节,包括FCγr型吞噬作用等。DENV-2-VERO感染可以部分缓解VERO细胞的免疫防御Denv-2-C6 / 36。结果表明,由两种DenV-2菌株诱导的不同的微小RNA变化可能与其感染能力部分相关。我们的数据提供了有用的见解,帮助阐明DenV感染后阐明的宿主病原体相互作用。

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