Taniguchi K, Nishikawa K, Urasawa T, Urasawa S, Midthun K, Kapikian A Z, Gorziglia M
Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20892.
J Virol. 1989 Sep;63(9):4101-6. doi: 10.1128/JVI.63.9.4101-4106.1989.
In our previous study (K. Taniguchi, Y. Morita, T. Urasawa, and S. Urasawa, J. Virol. 62:2421-2426, 1987) in which the cross-reactive neutralization epitopes on VP4 of human rotaviruses were analyzed, one strain, K8, was found to bear unique VP4 neutralization epitopes. This strain, which belongs to subgroup II and serotype 1, was not neutralized by any of six anti-VP4 neutralizing monoclonal antibodies which reacted with human rotavirus strains of serotypes 1, 3, and 4 or serotypes 1 through 4. We determined the complete nucleotide sequence of the gene encoding VP4 of strain K8 by primer extension. The VP4 gene is 2,359 base pairs in length, with 5' and 3' noncoding regions of 9 and 25 nucleotides, respectively. The gene contains a long open reading frame of 2,325 bases capable of coding for a protein of 775 amino acids. When compared with those of other human rotaviruses, VP4 of strain K8 had an insertion of one amino acid after residue 135, as found in simian rotavirus strains, and in addition, it had a deletion of one amino acid (residue 575). The amino acid homology of VP4 of strain K8 and those of other virulent human rotaviruses was only 60 to 70%. This was unusual, since over 90% VP4 homology has been found among the other virulent human rotavirus strains. In contrast, the VP7 amino acid sequence of the K8 strain was quite similar (over 98% homology) to those of other serotype 1 human rotaviruses. Thus, the K8 strain appears to have a unique VP4 gene previously not described.
在我们之前的研究中(K. 谷口、森田洋、浦泽彻和浦泽史,《病毒学杂志》62:2421 - 2426,1987年),对人轮状病毒VP4上的交叉反应中和表位进行了分析,发现一株名为K8的病毒带有独特的VP4中和表位。该毒株属于II亚组和1型血清型,不能被六种抗VP4中和单克隆抗体中的任何一种所中和,这些抗体可与人轮状病毒1、3和4型毒株或1至4型毒株发生反应。我们通过引物延伸法确定了K8毒株编码VP4的基因的完整核苷酸序列。VP4基因长度为2359个碱基对,5'和3'非编码区分别为9个和25个核苷酸。该基因包含一个2325个碱基的长开放阅读框,能够编码一个775个氨基酸的蛋白质。与其他人轮状病毒相比,K8毒株的VP4在第135位残基后插入了一个氨基酸,这与猿猴轮状病毒毒株的情况相同,此外,它还缺失了一个氨基酸(第575位残基)。K8毒株的VP4与其他致病性人轮状病毒的氨基酸同源性仅为60%至70%。这很不寻常,因为在其他致病性人轮状病毒毒株中发现的VP4同源性超过90%。相比之下,K8毒株的VP7氨基酸序列与其他1型血清型人轮状病毒的序列非常相似(同源性超过98%)。因此,K8毒株似乎具有一个以前未描述过的独特VP4基因。