Key result
Phylogenetic analysis of 113 rotavirus G1P[8] strains identified three lineages with a mean substitution rate of 7.25 × 10(-4) substitutions/site/year and mutations in neutralization domains.
Observational (n=113)
No
The most prevalent G1P[8] rotavirus lineage strains in Sapporo likely obtained survival advantages by changing the neutralization domains of VP7.
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Many studies indicate that G1P[8] genotypes are the most prevalent rotavirus strains worldwide. Although two vaccines have been licensed and their value proven in many countries, continuous surveillance for genetic evolution of circulating rotavirus strains before and after the introduction of the vaccines is desirable. G and P typing were carried out on all field strains isolated during 1987-2000 in Sapporo, Japan. Phylogenetic analysis for the VP7 gene of rotavirus G1P[8] strains was performed. Amino acid substitutions were mapped on the predicted three-dimensional VP7 protein image. G1P[8] genotype predominated. One hundred thirteen strains with G1P[8] genotype were analyzed. Phylogenetic studies of the VP7 gene classified these strains into three lineages. The mean estimated substitution rate was 7.25 × 10(-4) nucleotide substitutions per site per year. One predominant lineage contained the mutant strains which had VP7 amino acid substitutions at residue 91 and 212 that is in the neutralization domains. They were estimated to locate in or near intersubunit boundary of VP7 trimer. It is suggested that the most prevalent G1P[8] lineage strains in Sapporo obtained some survival advantages by changing the neutralization domains of VP7.
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Rotavirus G1P[8] evolution warrants continued surveillance; leaves open whether neutralization mutations affect current vaccine performance.
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Nagaoka et al. (2012) conducted an observational in Rotavirus infection (n=113). Rotavirus G1P[8] strains was evaluated on Phylogenetic lineages and VP7 gene substitution rate. Phylogenetic analysis of 113 rotavirus G1P[8] strains identified three lineages with a mean substitution rate of 7.25 × 10(-4) substitutions/site/year and mutations in neutralization domains.
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