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Sequence analysis of NSP4 gene of human rotavirus allows classification into two main genetic groups

轮状病毒 病毒学 遗传学 基因 序列(生物学) 生物 序列分析 呼肠孤病毒科 计算生物学 病毒
作者
Nigel A. Cunliffe,Patricia Woods,José Paulo Gagliardi Leite,Bimal Kumar Das,Mohanraj Ramachandran,M. K. Bhan,C. A. Hart,Roger I. Glass,Jon R. Gentsch
出处
期刊:Journal of Medical Virology [Wiley]
卷期号:53 (1): 41-50 被引量:84
标识
DOI:10.1002/(sici)1096-9071(199709)53:1<41::aid-jmv8>3.0.co;2-q
摘要

The rotavirus nonstructural glycoprotein NSP4 may represent the first identified viral enterotoxin. We have sequenced reverse transcription-polymerase chain reaction (RT-PCR)-generated fragments of 16 NSP4 genes of human rotavirus (HRV) strains from six different countries, representing seven different G and P type combinations. Based on the amount of sequence divergence between these and 11 previously sequenced NSP4 genes of human and animal rotaviruses, three distinct genetic groups could be recognized. Most strains within a group were closely related to each other at the nucleotide (nt) and amino acid (aa) levels (usually <10% divergence) but more distantly related (maximum 30.0% nt divergence and 24.7% aa divergence) to members of the other groups. Intergroup variation occurred in two highly variable regions of NSP4 (aa 16–34 and aa 131–148). The NSP4 “toxic peptide” (aa 114–135) exhibited aa variation at its carboxy terminus both within and between genetic groups. The largest group (genetic group II) contained HRV strains of subgroup II specificity (including genotypes P[8]G1, P[8]G3, P[6]G3, and P[8]G5 and serotype P8[11]G9), and the smaller group (genetic group I) contained HRV strains of subgroup I specificity (genotype P[4]G2). The NSP4 sequence of the rhesus rotavirus vaccine strain was distinct from all other strains and formed the third group (genetic group III). The NSP4 genes of animal rotaviruses UK, NCDV, and SA11 (genetic group I) and YM (genetic group II) and two possible human-animal rotavirus reassortant strains, Brazilian P[8]G5 and Indian P[11]G9 (genetic group II), could also be classified into one of these groups, suggesting a close evolutionary relationship between human and animal NSP4 genes. These results will facilitate studies of the host immune response to NSP4, which may be relevant to future HRV vaccine design. J. Med. Virol. 53:41–50, 1997. Published 1997 Wiley-Liss, Inc. This article was prepared by a group consisting of both United States government employees and non-United States government employees, and as such is subject to 17 U.S.C. Sec. 105.
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