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意大利导致婴幼儿出现脱水性腹泻的不常见 G9P[4]组 A 轮状病毒株。

Uncommon G9P[4] group A rotavirus strains causing dehydrating diarrhea in young children in Italy.

机构信息

Department of Food Safety, Nutrition and Veterinary Public Health, Istituto Superiore di Sanità, Rome, Italy.

Faculty of Medicine, Department of Biomedical Sciences and Public Health, Polytechnic University of Marche, Ancona, Italy.

出版信息

Infect Genet Evol. 2018 Oct;64:57-64. doi: 10.1016/j.meegid.2018.06.017. Epub 2018 Jun 20.

Abstract

Group A rotaviruses (RVA) are one of the major cause of acute gastroenteritis (AGE) in young children, being responsible for up to 250.000 deaths worldwide, mostly in developing countries. The two outer capsid proteins VP7 (glycoprotein, G-genotype) and VP4 (protease-sensitive protein, P-genotype) are the basis for the binary RVA nomenclature. Although at least 36 G-types and 51 P-types of rotavirus are presently known, most RVA infections in humans, worldwide as well as in Italy, are related to six major G/P combinations: G1P[8], G2P[4], G3P[8], G4P[8], G9P[8] and G12P[8]. In November 2016, in the framework of the Italian 2016/17 rotavirus surveillance season, a total of 22 rotavirus-positive samples from hospitalized children presenting AGE symptoms were collected in a small area of Central Italy (Ancona, Marche). After genotyping, 3 samples presented the G9P[4] genotype. In order to better understand the origin of these uncommon RVA strains causing dehydrating diarrhea in three children, the strains RVA/Human-wt/ITA/AN18/2016/G9P[4], RVA/Human-wt/ITA/AN19/2016/G9P[4] and RVA/Human-wt/ITA/AN22/2016/G9P[4] were subjected to nucleotide sequencing of all the 11 gene segments to define their genomic constellation. Nucleotide sequencing revealed that the genomic constellation of the three strains was G9-P[4]-I2-R2-C2-M2-A2-N2-T2-E2-H2, highlighting human origin for all the gene segments investigated. The molecular characterization of RVAs and the continue monitoring of their circulation is needed to better define the epidemiology of these pathogen and to detect the emergence of viral variants presenting a high spreading potential in humans in the post-vaccination era.

摘要

A 组轮状病毒(RVA)是导致婴幼儿急性肠胃炎(AGE)的主要原因之一,在全世界范围内造成多达 25 万例死亡,主要发生在发展中国家。两种外壳蛋白 VP7(糖蛋白,G 基因型)和 VP4(蛋白酶敏感蛋白,P 基因型)是轮状病毒二进制命名的基础。尽管目前已知至少有 36 种 G 型和 51 种 P 型轮状病毒,但全世界以及意大利的大多数人类轮状病毒感染都与六种主要的 G/P 组合有关:G1P[8]、G2P[4]、G3P[8]、G4P[8]、G9P[8]和 G12P[8]。2016 年 11 月,在意大利 2016/17 年轮状病毒监测季节框架内,在意大利中部一个小地区(安科纳,马尔凯)共收集了 22 份来自住院儿童 AGE 症状的轮状病毒阳性样本。基因分型后,3 份样本显示 G9P[4]基因型。为了更好地了解导致 3 名儿童出现脱水性腹泻的这些不常见轮状病毒株的起源,对 RVA/Human-wt/ITA/AN18/2016/G9P[4]、RVA/Human-wt/ITA/AN19/2016/G9P[4]和 RVA/Human-wt/ITA/AN22/2016/G9P[4]这 3 株轮状病毒进行了全基因组测序,以确定其基因组构成。核苷酸测序显示,这 3 株病毒的基因组构成均为 G9-P[4]-I2-R2-C2-M2-A2-N2-T2-E2-H2,提示所有研究基因片段均来源于人类。需要对 RVAs 进行分子特征分析并继续监测其传播,以更好地确定这些病原体的流行病学,并在疫苗接种后时代发现具有高传播潜力的病毒变异体。

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