Suppr超能文献

从手足口病患儿中分离的柯萨奇病毒 A6 株的特征。

Characterization of Coxsackievirus A6 Strains Isolated From Children With Hand, Foot, and Mouth Disease.

机构信息

Institute of Medical Biology, Chinese Academy of Medical Sciences, and Peking Union Medical College, Kunming, China.

Yunnan Key Laboratory of Vaccine Research Development on Severe Infectious Disease, Kunming, China.

出版信息

Front Cell Infect Microbiol. 2021 Aug 16;11:700191. doi: 10.3389/fcimb.2021.700191. eCollection 2021.

Abstract

Coxsackievirus A6 (CVA6) is a key pathogen causing hand, foot and mouth disease (HFMD). However, there are currently no specific antiviral drugs or vaccines for treating infections caused by CVA6. In this study, human rhabdomyosarcoma (RD), African green monkey kidney (Vero), and human embryonic lung diploid fibroblast (KMB17) cells were used to isolate CVA6 from 327 anal swab and fecal samples obtained during HFMD monitoring between 2009 and 2017. The VP1 genes of the isolates were sequenced and genotyped, and the biological characteristics of the representative CVA6 strains were analyzed. A total of 37 CVA6 strains of the D3 gene subtypes were isolated from RD cells, all of which belonged to the epidemic strains in mainland China. Using the adaptive culture method, 10 KMB17 cell-adapted strains were obtained; however, no Vero cell-adapted strains were acquired. Among the KMB17 cell-adapted strains, only KYN-A1205 caused disease or partial death in suckling mice, and its virulence was stronger than its RD cell-adapted strain. The pathogenic KYN-A1205 strain caused strong tropism to the muscle tissue and led to pathological changes, including muscle necrosis and nuclear fragmentation in the forelimb and hindlimb. Sequence analysis demonstrated that the KYN-A1205 strain exhibited multiple amino acid mutations after KMB17 cell adaptation. Moreover, it showed strong pathogenicity, good immunogenicity and genetic stability, and could be used as an experimental CVA6 vaccine candidate.

摘要

柯萨奇病毒 A6(Coxsackievirus A6,CVA6)是引起手足口病(hand, foot and mouth disease,HFMD)的关键病原体之一。然而,目前尚无针对 CVA6 感染的特效抗病毒药物或疫苗。本研究采用人横纹肌肉瘤(rhabdomyosarcoma,RD)、非洲绿猴肾(African green monkey kidney,Vero)和人胚肺二倍体成纤维细胞(human embryonic lung diploid fibroblast,KMB17),从 2009 年至 2017 年 HFMD 监测期间采集的 327 份肛拭子和粪便样本中分离 CVA6。对分离株的 VP1 基因进行测序和基因分型,并分析了代表性 CVA6 株的生物学特性。从 RD 细胞中分离出 37 株 D3 基因亚型的 CVA6 株,均属于中国大陆流行株。采用适应性培养方法获得 10 株 KMB17 细胞适应株,但未获得 Vero 细胞适应株。在 KMB17 细胞适应株中,仅 KYN-A1205 株能引起乳鼠发病或部分死亡,其毒力强于 RD 细胞适应株。致病性 KYN-A1205 株对肌肉组织具有强烈的嗜性,导致前肢和后肢肌肉坏死和核碎裂等病理变化。序列分析表明,KYN-A1205 株经 KMB17 细胞适应后存在多个氨基酸突变。该株具有较强的致病性、良好的免疫原性和遗传稳定性,可作为实验性 CVA6 疫苗候选株。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9ca/8418080/e824bb2fcd34/fcimb-11-700191-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验