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在支气管上皮细胞中,柯萨奇病毒 A10 感染后细胞 microRNAs 的综合分析和特征描述。

Comprehensive profiling and characterization of cellular microRNAs in response to coxsackievirus A10 infection in bronchial epithelial cells.

机构信息

Department of Pulmonary and Critical Care Medicine, The First People's Hospital of Yunnan Province, Kunming, China.

The Affiliated Hospital of Kunming University of Science and Technology, Kunming, Yunnan, China.

出版信息

Virol J. 2022 Jul 21;19(1):120. doi: 10.1186/s12985-022-01852-9.

Abstract

Coxsackievirus A10 (CV-A10), the causative agent of hand, foot, and mouth disease (HFMD), caused a series of outbreaks in recent years and often leads to neurological impairment, but a clear understanding of the disease pathogenesis and host response remains elusive. Cellular microRNAs (miRNAs), a large family of non-coding RNA molecules, have been reported to be key regulators in viral pathogenesis and virus-host interactions. However, the role of host cellular miRNAs defensing against CV-A10 infection is still obscure. To address this issue, we systematically analyzed miRNA expression profiles in CV-A10-infected 16HBE cells by high-throughput sequencing methods in this study. It allowed us to successfully identify 312 and 278 miRNAs with differential expression at 12 h and 24 h post-CV-A10 infection, respectively. Among these, 4 miRNAs and their target genes were analyzed by RT-qPCR, which confirmed the sequencing data. Gene target prediction and enrichment analysis revealed that the predicted targets of these miRNAs were significantly enriched in numerous cellular processes, especially in regulation of basic physical process, host immune response and neurological impairment. And the integrated network was built to further indicate the regulatory roles of miRNAs in host-CV-A10 interactions. Consequently, our findings could provide a beneficial basis for further studies on the regulatory roles of miRNAs relevant to the host immune responses and neuropathogenesis caused by CV-A10 infection.

摘要

柯萨奇病毒 A10(CV-A10)是手足口病(HFMD)的病原体,近年来引发了一系列疫情,常导致神经损伤,但对其发病机制和宿主反应仍缺乏清晰的认识。细胞 microRNAs(miRNAs)是一类非编码 RNA 分子大家族,据报道是病毒发病机制和病毒-宿主相互作用的关键调节因子。然而,宿主细胞 miRNAs 抵御 CV-A10 感染的作用仍不清楚。为了解决这个问题,我们在这项研究中通过高通量测序方法系统地分析了 CV-A10 感染 16HBE 细胞后的 miRNA 表达谱。这使我们能够成功识别出分别在 CV-A10 感染后 12 小时和 24 小时差异表达的 312 个和 278 个 miRNAs。其中,通过 RT-qPCR 分析了 4 个 miRNA 及其靶基因,验证了测序数据。基因靶标预测和富集分析表明,这些 miRNAs 的预测靶标显著富集在许多细胞过程中,尤其是在基本物理过程、宿主免疫反应和神经损伤的调节中。并构建了整合网络,以进一步表明 miRNAs 在宿主-CV-A10 相互作用中的调节作用。因此,我们的研究结果可为进一步研究 miRNA 与 CV-A10 感染引起的宿主免疫反应和神经发病机制的调节作用提供有益的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cca/9306089/e45c47fa45a7/12985_2022_1852_Fig1_HTML.jpg

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