Jameel Shahid, Zafrullah Mohammad, Chawla Yogesh K, Dilawari Jang B
Virology Group, International Centre for Genetic Engineering and Biotechnology, Aruna Asaf Ali Marg, New Delhi, India.
Virus Res. 2002 Jun;86(1-2):53-8. doi: 10.1016/s0168-1702(02)00052-7.
The genomic cloning and sequence of hepatitis E virus (HEV) from an epidemic in North India is reported. We describe here a simple method wherein the viral RNA was reverse transcribed and then amplified in a single step using an extra long polymerase chain reaction procedure. The full genome nucleotide sequence of this HEV isolate (called Yam-67) was made up of 7191 nucleotides, excepting the poly(A) tail and had three open reading frames: ORF1 coding for 1693 amino acids (aa), ORF2 coding for 659 aa and ORF3 coding for 122 aa. This North Indian isolate of HEV showed close sequence homology to other HEV isolates from India and Asia, but was distant from the Chinese genotype 4, Japanese, Mexican and US isolates. There is no indication from sequence analysis that this may be an atypical strain of HEV, as reported earlier.
报道了从印度北部一次疫情中分离出的戊型肝炎病毒(HEV)的基因组克隆及序列。我们在此描述一种简单方法,即使用超长聚合酶链反应程序,将病毒RNA逆转录后一步扩增。该HEV分离株(称为Yam - 67)的全基因组核苷酸序列由7191个核苷酸组成(不包括聚腺苷酸尾),有三个开放阅读框:ORF1编码1693个氨基酸(aa),ORF2编码659个aa,ORF3编码122个aa。该印度北部的HEV分离株与来自印度和亚洲的其他HEV分离株显示出密切的序列同源性,但与中国基因型4、日本、墨西哥和美国的分离株亲缘关系较远。序列分析未表明这可能是如先前报道的非典型HEV毒株。