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在肯尼亚沿海的基利菲,全国引入疫苗4年后,A组轮状病毒G3P[8]基因型的多重引入及优势地位

Multiple Introductions and Predominance of Rotavirus Group A Genotype G3P[8] in Kilifi, Coastal Kenya, 4 Years after Nationwide Vaccine Introduction.

作者信息

Mwanga Mike J, Verani Jennifer R, Omore Richard, Tate Jacqueline E, Parashar Umesh D, Murunga Nickson, Gicheru Elijah, Breiman Robert F, Nokes D James, Agoti Charles N

机构信息

Kenya Medical Research Institute (KEMRI)-Wellcome Trust Research Programme, off Hospital Road, Kilifi 80108, Kenya.

Centers for Disease Control and Prevention (CDC), KEMRI Complex, off Mbagathi Way, Village Market, Nairobi 00621, Kenya.

出版信息

Pathogens. 2020 Nov 24;9(12):981. doi: 10.3390/pathogens9120981.

DOI:10.3390/pathogens9120981
PMID:33255256
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7761311/
Abstract

Globally, rotavirus group A (RVA) remains a major cause of severe childhood diarrhea, despite the use of vaccines in more than 100 countries. RVA sequencing for local outbreaks facilitates investigation into strain composition, origins, spread, and vaccine failure. In 2018, we collected 248 stool samples from children aged less than 13 years admitted with diarrheal illness to Kilifi County Hospital, coastal Kenya. Antigen screening detected RVA in 55 samples (22.2%). Of these, VP7 (G) and VP4 (P) segments were successfully sequenced in 48 (87.3%) and phylogenetic analysis based on the VP7 sequences identified seven genetic clusters with six different GP combinations: G3P[8], G1P[8], G2P[4], G2P[8], G9P[8] and G12P[8]. The G3P[8] strains predominated the season ( = 37, 67.2%) and comprised three distinct G3 genetic clusters that fell within Lineage I and IX (the latter also known as equine-like G3 Lineage). Both the two G3 lineages have been recently detected in several countries. Our study is the first to document African children infected with G3 Lineage IX. These data highlight the global nature of RVA transmission and the importance of increasing global rotavirus vaccine coverage.

摘要

在全球范围内,尽管已有100多个国家使用了疫苗,但A组轮状病毒(RVA)仍然是导致儿童严重腹泻的主要原因。对本地疫情进行RVA测序有助于调查毒株组成、起源、传播及疫苗失效情况。2018年,我们从肯尼亚沿海基利菲县医院收治的腹泻病患儿中收集了248份13岁以下儿童的粪便样本。抗原筛查在55份样本(22.2%)中检测到RVA。其中,48份样本(87.3%)成功对VP7(G)和VP4(P)片段进行了测序,基于VP7序列的系统发育分析确定了7个遗传簇,有6种不同的GP组合:G3P[8]、G1P[8]、G2P[4]、G2P[8]、G9P[8]和G12P[8]。G3P[8]毒株在该季节占主导地位(n = 37,67.2%),包括三个不同的G3遗传簇,它们属于谱系I和IX(后者也称为类马G3谱系)。最近在几个国家都检测到了这两个G3谱系。我们的研究首次记录了感染G3谱系IX的非洲儿童。这些数据凸显了RVA传播的全球性以及提高全球轮状病毒疫苗覆盖率的重要性。

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