Ray R, Jameel S, Manivel V, Ray R
International Centre for Genetic Engineering and Biotechnology, New Delhi, India.
Virology. 1992 Jul;189(1):359-62. doi: 10.1016/0042-6822(92)90716-3.
Enterically transmitted non-A, non-B hepatitis virus (HEV), the causative agent for sporadic and large epidemic outbreaks in developing countries, contains a positive-sense single-stranded RNA genome. The genome of the virus encodes three open reading frames (ORF1, ORF2, and ORF3). The gene segment corresponding to the small open reading frame (ORF3), overlapping between ORF1 and ORF2, was synthesized by reverse transcription-polymerase chain reaction (RT-PCR) from a number of previously identified HEV-positive clinical specimens. A DNA fragment of 166 bp was consistently obtained from all the clinical specimens. This small fragment was cloned, sequenced, and found to contain an open reading frame encoding only 41 amino acid residues. Comparison of our results with that of geographically related Burma HEV suggests a major inframe deletion of 246 bp in the ORF3 of Indian strain. The protein encoded by ORF3 does not appear to be useful for early serodiagnosis as a synthetic peptide deduced from the truncated ORF3 failed to show any demonstrable immunoreactivity against HEV-infected acute phase sera in an enzyme-linked immunosorbent assay.
肠道传播的非甲非乙型肝炎病毒(HEV)是发展中国家散发性和大规模流行疫情的病原体,其基因组为正链单链RNA。该病毒的基因组编码三个开放阅读框(ORF1、ORF2和ORF3)。对应于小开放阅读框(ORF3)的基因片段,在ORF1和ORF2之间重叠,通过逆转录聚合酶链反应(RT-PCR)从多个先前鉴定的HEV阳性临床标本中合成。从所有临床标本中一致获得了一个166 bp的DNA片段。这个小片段被克隆、测序,发现包含一个仅编码41个氨基酸残基的开放阅读框。将我们的结果与地理上相关的缅甸HEV的结果进行比较,表明印度毒株的ORF3中有一个246 bp的主要框内缺失。由ORF3编码的蛋白质似乎对早期血清学诊断无用,因为从截短的ORF3推导的合成肽在酶联免疫吸附试验中未能显示出对HEV感染急性期血清的任何可证明的免疫反应性。