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系统发育分析表明,衣壳蛋白以外的因素在GII.2型诺如病毒的流行潜力中起作用。

Phylogenetic Analyses Suggest that Factors Other Than the Capsid Protein Play a Role in the Epidemic Potential of GII.2 Norovirus.

作者信息

Tohma Kentaro, Lepore Cara J, Ford-Siltz Lauren A, Parra Gabriel I

机构信息

Division of Viral Products, Food and Drug Administration, Silver Spring, Maryland, USA.

出版信息

mSphere. 2017 May 17;2(3). doi: 10.1128/mSphereDirect.00187-17. eCollection 2017 May-Jun.

Abstract

Norovirus is the leading cause of acute gastroenteritis worldwide. For over two decades, a single genotype (GII.4) has been responsible for most norovirus-associated cases. However, during the winter of 2014 to 2015, the GII.4 strains were displaced by a rarely detected genotype (GII.17) in several countries of the Asian continent. Moreover, during the winter of 2016 to 2017, the GII.2 strain reemerged as predominant in different countries worldwide. This reemerging GII.2 strain is a recombinant virus that presents a GII.P16 polymerase genotype. In this study, we investigated the evolutionary dynamics of GII.2 to determine the mechanism of this sudden emergence in the human population. The phylogenetic analyses indicated strong linear evolution of the VP1-encoding sequence, albeit with minor changes in the amino acid sequence over time. Without major genetic differences among the strains, a clustering based on the polymerase genotype was observed in the tree. This association did not affect the substitution rate of the VP1. Phylogenetic analyses of the polymerase region showed that reemerging GII.P16-GII.2 strains diverged into a new cluster, with a small number of amino acid substitutions detected on the surface of the associated polymerase. Thus, besides recombination or antigenic shift, point mutations in nonstructural proteins could also lead to novel properties with epidemic potential in different norovirus genotypes. Noroviruses are a major cause of gastroenteritis worldwide. Currently, there is no vaccine or specific antiviral available to treat norovirus disease. Multiple norovirus strains infect humans, but a single genotype (GII.4) has been regarded as the most important cause of viral gastroenteritis outbreaks worldwide. Its persistence and predominance have been explained by the continuous replacement of variants that present new antigenic properties on their capsid protein, thus evading the herd immunity acquired to the previous variants. Over the last three seasons, minor genotypes have displaced the GII.4 viruses as the predominant strains. One of these genotypes, GII.2, reemerged as predominant during 2016 to 2017. Here we show that factors such as minor changes in the polymerase may have driven the reemergence of GII.2 during the last season. A better understanding of norovirus diversity is important for the development of effective treatments against noroviruses.

摘要

诺如病毒是全球急性胃肠炎的主要病因。二十多年来,单一基因型(GII.4)导致了大多数与诺如病毒相关的病例。然而,在2014年至2015年冬季,亚洲大陆几个国家中,GII.4毒株被一种罕见的基因型(GII.17)所取代。此外,在2016年至2017年冬季,GII.2毒株在全球不同国家再次成为优势毒株。这种再次出现的GII.2毒株是一种重组病毒,具有GII.P16聚合酶基因型。在本研究中,我们调查了GII.2的进化动态,以确定其在人群中突然出现的机制。系统发育分析表明,编码VP1的序列呈强烈的线性进化,尽管随着时间的推移氨基酸序列变化较小。菌株之间没有重大的遗传差异,但在树形图中观察到基于聚合酶基因型的聚类。这种关联并不影响VP1的替换率。聚合酶区域的系统发育分析表明,再次出现的GII.P16-GII.2毒株分化为一个新的聚类,在相关聚合酶表面检测到少量氨基酸替换。因此,除了重组或抗原转变外,非结构蛋白中的点突变也可能导致不同诺如病毒基因型中具有流行潜力的新特性。诺如病毒是全球胃肠炎的主要病因。目前,尚无疫苗或特异性抗病毒药物可用于治疗诺如病毒疾病。多种诺如病毒毒株感染人类,但单一基因型(GII.4)被认为是全球病毒性胃肠炎暴发的最重要病因。其持续性和优势地位可通过不断替换衣壳蛋白上具有新抗原特性的变体来解释,从而逃避对先前变体产生的群体免疫。在过去三个季节中,次要基因型已取代GII.4病毒成为优势毒株。其中一种基因型GII.2在2016年至2017年期间再次成为优势毒株。在这里我们表明,聚合酶的微小变化等因素可能推动了上一季GII.2的再次出现。更好地了解诺如病毒的多样性对于开发有效的抗诺如病毒治疗方法很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc39/5437133/776394590f9b/sph0031722860001.jpg

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