Blomqvist Soile, Bruu Anne-Lise, Stenvik Mirja, Hovi Tapani
Department of Microbiology, Enterovirus Laboratory, National Public Health Institute (KTL), Mannerheimintie 166, 00300 Helsinki, Finland.
National Institute of Public Health, Oslo, Norway.
J Gen Virol. 2003 Mar;84(Pt 3):573-580. doi: 10.1099/vir.0.18708-0.
A Sabin 3/Sabin 2/Sabin 3 (S3/2/3) intertypic recombinant poliovirus was isolated from a faecal specimen from a 2-year-old healthy boy approximately 12 weeks after administration of oral poliovirus vaccine. The first recombination junction was in the genomic region encoding the VP1 capsid protein between nucleotide positions 3274 and 3285 (numbering according to Sabin 3) and the second was in the RNA polymerase region (nucleotide positions 6824 and 6825). The recombination had introduced six Sabin 2-derived amino acids into the Sabin 3 capsid environment in the carboxyl terminus of VP1. The complete genome of the recombinant virus differed from corresponding parental Sabin strains at 33 nucleotide positions, nine of them resulting in an amino acid substitution. Four substitutions were in the capsid proteins and five were in the region encoding the non-structural proteins. One amino acid was changed in the antigenic site 2B and two in site 3B. In addition, the whole antigenic site 3A was replaced by Sabin 2-specific amino acids, but the antigenic characteristics of the S3/2/3 did not show type 2-specific features. Neutralizing antibody titres in sera from Finnish children immunized with the inactivated poliovirus vaccine were not lower against the recombinant virus than against Sabin 3. Our results suggest that the chimeric virus was most likely generated by recombination events in the vaccinee, rather than representing progeny of circulating vaccine-derived virus.
在一名2岁健康男孩口服脊髓灰质炎疫苗约12周后,从其粪便标本中分离出一株萨宾3型/萨宾2型/萨宾3型(S3/2/3)型间重组脊髓灰质炎病毒。第一个重组位点位于编码VP1衣壳蛋白的基因组区域,核苷酸位置在3274和3285之间(根据萨宾3型编号),第二个位于RNA聚合酶区域(核苷酸位置6824和6825)。重组在VP1羧基末端的萨宾3型衣壳环境中引入了6个源自萨宾2型的氨基酸。重组病毒的完整基因组与相应亲本萨宾毒株在33个核苷酸位置存在差异,其中9个导致氨基酸替换。4个替换发生在衣壳蛋白中,5个在编码非结构蛋白的区域。抗原位点2B中有1个氨基酸发生改变,位点3B中有2个。此外,整个抗原位点3A被萨宾2型特异性氨基酸取代,但S3/2/3的抗原特性未显示出2型特异性特征。用灭活脊髓灰质炎疫苗免疫的芬兰儿童血清中针对重组病毒的中和抗体滴度并不低于针对萨宾3型的滴度。我们的结果表明,嵌合病毒很可能是由受种者体内的重组事件产生的,而不是循环疫苗衍生病毒的子代。