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黎巴嫩住院 5 岁以下儿童中人类轮状病毒 A 的遗传多样性。

Genetic Diversity of Human Rotavirus A Among Hospitalized Children Under-5 Years in Lebanon.

机构信息

Faculty of Medicine, Center for Infectious Diseases Research, American University of Beirut, Beirut, Lebanon.

Department of Pediatrics and Adolescent Medicine, Faculty of Medicine, American University of Beirut, Beirut, Lebanon.

出版信息

Front Immunol. 2020 Feb 26;11:317. doi: 10.3389/fimmu.2020.00317. eCollection 2020.

Abstract

Human rotavirus remains a major cause of gastroenteritis worldwide despite the availability of effective vaccines. In this study, we investigated the genetic diversity of rotaviruses circulating in Lebanon. We genetically characterized the VP4 and VP7 genes encoding the outer capsid proteins of 132 rotavirus-associated gastroenteritis specimens, previously identified in hospitalized children (<5 years) from 2011 to 2013 in Lebanon. These included 43 vaccine-breakthrough specimens and the remainder were from non-vaccinated subjects. Phylogenetic analysis of VP4 and VP7 genes revealed distinct clustering compared to the vaccine strains, and several substitutions were identified in the antigenic epitopes of Lebanese specimens. No unique changes were identified in the breakthrough specimens compared to non-breakthroughs that could explain the occurrence of infection in vaccinated children. Further, we report the emergence of a rare P[8] OP354-like strain with a G9 VP7 in Lebanon, possessing high genetic variability in their VP4 compared to vaccine strains. Therefore, human rotavirus strains circulating in Lebanon and globally have accumulated numerous substitutions in their antigenic sites compared to those currently used in the licensed vaccines. The successful spread and continued genetic drift of these strains over time might undermine the effectiveness of the vaccines. The effect of such changes in the antigenic sites on vaccine efficacy remains to be assessed.

摘要

尽管已有有效的疫苗,但人类轮状病毒仍然是全球范围内引起肠胃炎的主要原因。在本研究中,我们调查了在黎巴嫩流行的轮状病毒的遗传多样性。我们对从 2011 年至 2013 年期间在黎巴嫩住院的<5 岁儿童中先前鉴定出的 132 例轮状病毒相关肠胃炎标本的 VP4 和 VP7 基因(编码外壳蛋白)进行了基因特征分析。这些标本包括 43 例疫苗突破性标本,其余标本来自未接种疫苗的个体。VP4 和 VP7 基因的系统发育分析显示与疫苗株相比存在明显的聚类,并且在黎巴嫩标本的抗原表位中发现了几个取代。与非突破性标本相比,突破性标本中未发现能解释接种儿童感染发生的独特变化。此外,我们报告了在黎巴嫩出现了一种罕见的 P[8] OP354 样株,其 G9 VP7 具有与疫苗株相比在其 VP4 中更高的遗传变异性。因此,与目前在许可疫苗中使用的疫苗相比,在黎巴嫩和全球流行的人类轮状病毒株在其抗原位点积累了许多取代。这些菌株随着时间的推移成功传播和持续遗传漂移可能会削弱疫苗的有效性。抗原位点的这种变化对疫苗效力的影响仍有待评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b41/7054381/39a994c940f6/fimmu-11-00317-g0001.jpg

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