Molecular characterisation of the NSP4 gene of group A human rotavirus G2P[4] strains circulating in São Paulo, Brazil, from 1994 and 2006 to 2010
Group A human rotaviruses (HuRVA) are causative agents of acute gastroenteritis. Six viral structural proteins (VPs) and six nonstructural proteins (NSPs) are produced in RV-infected cells. NSP4 is a diarrhoea-inducing viral enterotoxin and NSP4 gene analysis revealed at least 15 (E1-E15) genotypes....
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Veröffentlicht in: | Memórias do Instituto Oswaldo Cruz 2015-09, Vol.110 (6), p.786-792 |
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Zusammenfassung: | Group A human rotaviruses (HuRVA) are causative agents of acute
gastroenteritis. Six viral structural proteins (VPs) and six
nonstructural proteins (NSPs) are produced in RV-infected cells. NSP4
is a diarrhoea-inducing viral enterotoxin and NSP4 gene analysis
revealed at least 15 (E1-E15) genotypes. This study analysed the NSP4
genetic diversity of HuRVA G2P[4] strains collected in the state of
São Paulo (SP) from 1994 and 2006-2010 using reverse
transcription-polymerase chain reaction, sequencing and phylogenetic
analysis. Forty (97.6%) G2P[4] strains displayed genotype E2; one
strain (2.4%) displayed genotype E1. These results are consistent with
the proposed linkage between VP4/VP7 (G2P[4]) and the NSP4 (E2)
genotype of HuRVA. NSP4 phylogenetic analysis showed distinct clusters,
with grouping of most strains by their genotype and collection year,
and most strains from SP were clustered together with strains from
other Brazilian states. A deduced amino acid sequence alignment for E2
showed many variations in the C-terminal region, including the
VP4-binding domain. Considering the ability of NSP4 to generate host
immunity, monitoring NSP4 variations, along with those in the VP4 or
VP7 protein, is important for evaluating the circulation and
pathogenesis of RV. Finally, the presence of one G2P[4]E1 strain
reinforces the idea that new genotype combinations emerge through
reassortment and independent segregation. |
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ISSN: | 1678-8060 0074-0276 1678-8060 0074-0276 |
DOI: | 10.1590/0074-02760150199 |