Literature DB >> 12727352

VP7 gene polymorphism of serotype G9 rotavirus strains and its impact on G genotype determination by PCR.

Norma Santos1, Eduardo M Volotão, Caroline C Soares, Maria Carolina M Albuquerque, Fabiano M da Silva, Vladimir Chizhikov, Yasutaka Hoshino.   

Abstract

Rotaviruses are the single most important etiologic agents of severe diarrhea of infants and young children worldwide. Surveillance of rotavirus serotypes/genotypes (both VP7[G] and VP4[P]) is in progress globally in which polymerase chain reaction (PCR) has been the assay of choice. We investigated polymorphism of the VP7 gene of serotype G9 rotavirus strains and its impact on the determination of VP7 gene genotype by PCR assay. By VP7 gene sequence analysis, we and others have previously shown that the G9 rotavirus strains belong to one of three VP7 gene lineages. By PCR assay using three different sets of commonly used primers specific for G1-4, 8 and 9, 23 Brazilian G9 strains and 5 well-characterized prototype G9 strains which collectively represented all three VP7 gene lineages were typed as: (i) G3; (ii) G4; (iii) G9; (iv) G3 and G9; or (v) G9 and G4 depending on a primer pool employed. This phenomenon appeared to be due to: (i) a VP7 gene lineage-specific polymorphism, more specifically mutation(s) in the primer binding region of the VP7 gene of G9 strain; and (ii) the magnitude of difference in nucleotide homology at respective primer binding site between homotypic (G9) and heterotypic (G3 or G4) primers present in a primer pool employed.

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Year:  2003        PMID: 12727352     DOI: 10.1016/s0168-1702(02)00318-0

Source DB:  PubMed          Journal:  Virus Res        ISSN: 0168-1702            Impact factor:   3.303


  6 in total

1.  Predominance of rotavirus genotype G9 during the 1999, 2000, and 2002 seasons among hospitalized children in the city of Salvador, Bahia, Brazil: implications for future vaccine strategies.

Authors:  Norma Santos; Eduardo M Volotão; Caroline C Soares; Gúbio S Campos; Silvia Ines Sardi; Yasutaka Hoshino
Journal:  J Clin Microbiol       Date:  2005-08       Impact factor: 5.948

2.  Development and validation of DNA microarray for genotyping group A rotavirus VP4 (P[4], P[6], P[8], P[9], and P[14]) and VP7 (G1 to G6, G8 to G10, and G12) genes.

Authors:  Shinjiro Honma; Vladimir Chizhikov; Norma Santos; Masatoshi Tatsumi; Maria do Carmo S T Timenetsky; Alexandre C Linhares; Joana D'Arc P Mascarenhas; Hiroshi Ushijima; George E Armah; Jon R Gentsch; Yasutaka Hoshino
Journal:  J Clin Microbiol       Date:  2007-06-13       Impact factor: 5.948

3.  Rotavirus serotype G9 strains belonging to VP7 gene phylogenetic sequence lineage 1 may be more suitable for serotype G9 vaccine candidates than those belonging to lineage 2 or 3.

Authors:  Yasutaka Hoshino; Ronald W Jones; Jerri Ross; Shinjiro Honma; Norma Santos; Jon R Gentsch; Albert Z Kapikian
Journal:  J Virol       Date:  2004-07       Impact factor: 5.103

4.  Characterization of novel VP7, VP4, and VP6 genotypes of a previously untypeable group A rotavirus.

Authors:  Owen D Solberg; Maria Eloisa Hasing; Gabriel Trueba; Joseph N S Eisenberg
Journal:  Virology       Date:  2009-01-08       Impact factor: 3.616

5.  Nucleotide mismatches between the VP7 gene and the primer are associated with genotyping failure of a specific lineage from G1 rotavirus strains.

Authors:  Gabriel I Parra; Emilio E Espinola
Journal:  Virol J       Date:  2006-05-25       Impact factor: 4.099

6.  Inaccurate identification of rotavirus genotype G9 as genotype G3 strains due to primer mismatch.

Authors:  Marcelo Takahiro Mitui; Tga Nilmini Chandrasena; Paul Ks Chan; Shaman Rajindrajith; E Anthony S Nelson; Ting Fan Leung; Akira Nishizono; Kamruddin Ahmed
Journal:  Virol J       Date:  2012-08-03       Impact factor: 4.099

  6 in total

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