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首页> 外文期刊>Emerging Infectious Diseases >Detection of Rare G3P[19] Group A Rotavirus in Human Patient, Italy (http://wwwnc.cdc.gov/eid/article/20/11/13-1699)
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Detection of Rare G3P[19] Group A Rotavirus in Human Patient, Italy (http://wwwnc.cdc.gov/eid/article/20/11/13-1699)

机译:在意大利人类患者中检测到罕见的G3P [19] A型轮状病毒(http://wwwnc.cdc.gov/eid/article/20/11/13-1699)

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摘要

Group A rotavirus (RVA) is the leading cause of acute gastroenteritis in children <5 years of age worldwide, causing ≈450,000 deaths annually. The RVA genome is composed of 11 double-stranded RNA segments, encoding 6 structural viral (VP) and 5 nonstructural (NS) proteins (1). The outer capsid proteins, VP7 and VP4, elicit neutralizing antibodies. The genes encoding these proteins specify at least 27 G and 37 P genotypes, which are used for RVA binary classification. Most RVA human infections worldwide are related to 5 major genotypes: G1P[8], G2P[4], G3P[8], G4P[8], and G9P[8] (2). Genome segment reassortment between human strains or human and animal strains during co-infections can generate viruses with novel genotype combinations, possibly influencing the virus phenotype (2). Some human and animal RVA strains possess unusual genotype combinations (3,4), and some strains might partially escape vaccine- induced immune protection (5).
机译:轮状病毒A组轮状病毒(RVA)是全球<5岁儿童急性胃肠炎的主要原因,每年造成约45万例死亡。 RVA基因组由11个双链RNA片段组成,编码6个结构性病毒(VP)和5个非结构性(NS)蛋白(1)。外衣壳蛋白VP7和VP4引发中和抗体。编码这些蛋白质的基因至少指定了27 G和37 P基因型,用于RVA二进制分类。全球大多数RVA人类感染与5种主要基因型有关:G1P [8],G2P [4],G3P [8],G4P [8]和G9P [8](2)。在共同感染过程中,人类品系或人类和动物品系之间的基因组片段重排可以产生具有新基因型组合的病毒,可能会影响病毒表型(2)。一些人和动物的RVA菌株具有不同寻常的基因型组合(3,4),而某些菌株可能部分逃避了疫苗诱导的免疫保护(5)。

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