Reyes G R, Yarbough P O, Tam A W, Purdy M A, Huang C C, Kim J S, Bradley D W, Fry K E
Molecular Virology Department, Genelabs Incorporated, Redwood City, CA 94063.
Gastroenterol Jpn. 1991 Jul;26 Suppl 3:142-7. doi: 10.1007/BF02779285.
A normally endemic form of viral hepatitis is the cause of major epidemic outbreaks in developing countries. This disease has a global distribution and has been referred to as water-borne, epidemic or enterically transmitted non-A, non-B hepatitis (ET-NANBH). Although the fecal-oral route of transmission predominates, person-to-person routes of exposure were also suggested in some epidemiologic studies. The disease has been documented as having an extremely high mortality in pregnant women (approximately 20%). Sporadic cases of ET-NANBH, as well as imported travel exposures, have been reported in developed countries. Molecular cloning was hampered by the lack of a tissue culture system for virus propagation, however, an available animal model and a newly developed non-specific amplification procedure were used to clone and identify an exogenous cDNA (ET1.1) from a Burma-isolate infected animal. Molecular clones were also identified by immunoscreening of a cDNA library made from a fecal specimen collected from a Mexican outbreak of ET-NANBH. The isolation and sequencing of a set of overlapping cDNA clones had led to the recognition that this form of hepatitis is caused by a virus unlike any of the other viral hepatitis agents. The molecular characterization of HEV will lead to important pathobiologic insights and hasten the development of potentially useful diagnostic and therapeutic products for ET-NANBH.
一种通常呈地方性流行的病毒性肝炎是发展中国家重大疫情爆发的原因。这种疾病在全球范围内都有分布,曾被称为水源性、流行性或经肠道传播的非甲非乙型肝炎(ET-NANBH)。尽管粪-口传播途径占主导,但一些流行病学研究也提示了人与人之间的接触途径。据记载,该疾病在孕妇中的死亡率极高(约20%)。发达国家也报告了ET-NANBH的散发病例以及输入性旅行感染病例。由于缺乏用于病毒繁殖的组织培养系统,分子克隆受到阻碍,不过,利用一种可用的动物模型和新开发的非特异性扩增程序,从一只感染缅甸分离株的动物身上克隆并鉴定出了一个外源性cDNA(ET1.1)。通过对从墨西哥ET-NANBH疫情中采集的粪便标本构建的cDNA文库进行免疫筛选,也鉴定出了分子克隆。一组重叠cDNA克隆的分离和测序使得人们认识到,这种形式的肝炎是由一种与其他病毒性肝炎病原体不同的病毒引起的。戊型肝炎病毒(HEV)的分子特征将带来重要的病理生物学见解,并加速开发针对ET-NANBH的潜在有用的诊断和治疗产品。