Urasawa T, Urasawa S, Chiba Y, Taniguchi K, Kobayashi N, Mutanda L N, Tukei P M
Department of Hygiene, Sapporo Medical College, Japan.
J Clin Microbiol. 1987 Oct;25(10):1891-6. doi: 10.1128/jcm.25.10.1891-1896.1987.
The electropherotypes of human rotavirus RNAs from 100 diarrheic stool specimens collected in two major districts of Kenya from 1982 to 1983 were previously reported (Y. Chiba, C. Miyazaki, Y. Makino, L. N. Mutanda, A. Kibue, E. O. Lichenga, and P. M. Tukei, J. Clin. Microbiol. 19:579-582, 1984). Of these specimens, 25 that contained rotaviruses with different RNA electropherotypes were subjected to a virus isolation experiment with MA-104 cells, and 16 rotavirus strains were isolated. The use of an enzyme-linked immunosorbent assay with subgroup-specific monoclonal antibodies enabled us to successfully subgroup 15 isolates: 4 in subgroup I and 11 in subgroup II. By fluorescent-focus-neutralization test with serotype-specific rabbit antisera, 13 isolates could be serotyped: 7 as serotype 1, 4 as serotype 2, and 2 as serotype 3. Of the remaining three isolates, F153, F247, and G402, the former was doubly neutralizable with serotype 1 and serotype 4 antisera and the latter two were neutralizable with serotype 3 and serotype 4 antisera. Detailed analysis with the antisera against F153 and F247 and four serotype-specific, VP7-directed monoclonal antibodies suggested that F153 is a serotypic mosaic strain with serotype 4-specific VP3 and serotype 1-specific VP7 outer capsid proteins and F247 and G402 are possibly antigenic mosaic strains with serotype 3 and serotype 4 antigens. On the basis of the correspondence of the rotavirus isolate serotypes determined in this study to the electropherotypes reported previously, it was inferred that serotype 1 strains were most prevalent in two districts of Kenya from 1982 to 1983, followed by any type of serotypic mosaic strains.
先前已报道了1982年至1983年在肯尼亚两个主要地区收集的100份腹泻粪便标本中人类轮状病毒RNA的电泳图谱(千叶洋、宫崎彻、牧野洋、穆坦达·L·N、基布埃·A、利琴加·E·O和图凯·P·M,《临床微生物学杂志》19:579 - 582,1984年)。在这些标本中,选取25份含有不同RNA电泳图谱的轮状病毒的标本,用MA - 104细胞进行病毒分离实验,分离出16株轮状病毒。使用具有亚组特异性单克隆抗体的酶联免疫吸附测定法,我们成功地将15株分离株进行了亚组分类:4株属于I亚组,11株属于II亚组。通过用血清型特异性兔抗血清进行荧光灶中和试验,13株分离株可以进行血清型分类:7株为血清型1,4株为血清型2,2株为血清型3。其余三株分离株F153、F247和G402中,前者能用血清型1和血清型4抗血清双重中和,后两者能用血清型3和血清型4抗血清中和。用针对F153和F247的抗血清以及四种血清型特异性、针对VP7的单克隆抗体进行的详细分析表明,F153是一种血清型嵌合株,具有血清型4特异性的VP3和血清型1特异性的VP7外衣壳蛋白,F247和G402可能是具有血清型3和血清型4抗原的抗原嵌合株。根据本研究中确定的轮状病毒分离株血清型与先前报道的电泳图谱的对应关系,推断出1982年至1983年血清型1毒株在肯尼亚两个地区最为普遍,其次是任何类型的血清型嵌合株。