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疫苗时代之后轮状病毒的多样性与进化

Rotavirus diversity and evolution in the post-vaccine world.

作者信息

Patton John T

机构信息

Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

Discov Med. 2012 Jan;13(68):85-97.

Abstract

Rotaviruses (RVs) are a large genetically diverse population of segmented double-stranded (ds) RNA viruses that are important causes of gastroenteritis in many animal species. The human RVs are responsible for the deaths of nearly 450,000 infants and young children each year, most occurring in developing countries. Recent large-scale sequencing efforts have revealed that the genomes of human RVs typically consist of phylogenetically linked constellations of eleven dsRNA segments. The presence of such preferred constellations indicate that the human RV genes have co-evolved to produce protein sets that work optimally together to support virus replication. Two of the viral genes encode virion outer capsid proteins (VP7 and VP4) whose antigenic properties define the G/P type of the virus. From year-to-year and place-to-place, the G/P type of human RVs associated with disease can fluctuate dramatically, phenomena that can be associated with the presence and behavior of genetically distinct RV clades. The recent introduction of two live attenuated RV vaccines [RotaTeq (TM) and Rotarix (TM)] into the childhood vaccination programs of various countries has been highly effective in reducing the incidence of RV diarrheal disease. Whether the widespread use of these vaccines will introduce selective pressures on human RVs, triggering genetic and antigenic changes that undermine the effectiveness of vaccinations programs, is uncertain and will require continued surveillance of human RVs.

摘要

轮状病毒(RVs)是一大类基因多样的分段双链(ds)RNA病毒,是许多动物物种肠胃炎的重要病因。人类轮状病毒每年导致近45万婴幼儿死亡,其中大多数发生在发展中国家。最近的大规模测序工作表明,人类轮状病毒的基因组通常由11个dsRNA片段的系统发育相关星座组成。这种优选星座的存在表明,人类轮状病毒基因共同进化以产生能最佳协同工作以支持病毒复制的蛋白质组。其中两个病毒基因编码病毒粒子外衣壳蛋白(VP7和VP4),其抗原特性决定了病毒的G/P类型。在不同年份和不同地点,与疾病相关的人类轮状病毒的G/P类型可能会发生巨大波动,这种现象可能与基因不同的轮状病毒进化枝的存在和行为有关。最近,两种减毒活轮状病毒疫苗[Rotateq(TM)和Rotarix(TM)]被引入各国的儿童疫苗接种计划,在降低轮状病毒腹泻疾病的发病率方面非常有效。这些疫苗的广泛使用是否会给人类轮状病毒带来选择压力,引发基因和抗原变化,从而削弱疫苗接种计划的有效性,目前尚不确定,需要对人类轮状病毒进行持续监测。

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