South African G4P[6] asymptomatic and symptomatic neonatal rotavirus strains differ in their NSP4, VP8*, and VP7 genes
Cara T. Pager
MRC/MEDUNSA Diarrhoeal Pathogens Research Unit, MEDUNSA, Pretoria, South Africa
Department of Microbiology, University of the Witwatersrand, Johannesburg, South Africa
Search for more papers by this authorJennifer J. Alexander
Department of Microbiology, University of the Witwatersrand, Johannesburg, South Africa
Search for more papers by this authorCorresponding Author
A. Duncan Steele
MRC/MEDUNSA Diarrhoeal Pathogens Research Unit, MEDUNSA, Pretoria, South Africa
MRC/MEDUNSA Diarrhoeal Pathogens Research Unit, PO Box 173, MEDUNSA 0204, South Africa===Search for more papers by this authorCara T. Pager
MRC/MEDUNSA Diarrhoeal Pathogens Research Unit, MEDUNSA, Pretoria, South Africa
Department of Microbiology, University of the Witwatersrand, Johannesburg, South Africa
Search for more papers by this authorJennifer J. Alexander
Department of Microbiology, University of the Witwatersrand, Johannesburg, South Africa
Search for more papers by this authorCorresponding Author
A. Duncan Steele
MRC/MEDUNSA Diarrhoeal Pathogens Research Unit, MEDUNSA, Pretoria, South Africa
MRC/MEDUNSA Diarrhoeal Pathogens Research Unit, PO Box 173, MEDUNSA 0204, South Africa===Search for more papers by this authorAbstract
Over the past decade, a G4P[6] strain has been found to be circulating in different neonatal wards in the Pretoria area. This endemic strain was associated with both asymptomatic and symptomatic infection, providing the opportunity to undertake a molecular study of some of the putative “virulence” genes. The genes encoding NSP4, VP8*, and VP7 of two asymptomatic and two Symptomatic strains were sequenced and compared with ST3. Within each of these genes, amino acid substitutions unique to South African strains were recorded. Four conserved amino acid differences between asymptomatic and symptomatic strains at aa 82 (serine to leucine), aa 114 (aspartic acid to glutamic acid), aa 138 (proline to threonine), and aa 169 (leucine to serine) were identified within the NSP4 gene. The hypervariable region of VP8* exhibited 10 specific amino acid differences (at aa 73, 78, 98, 111, 116, 142, 145, 167, 169, and 188) between asymptomatic and symptomatic strains, while three amino acid substitutions within VP7 were noted. These changes to VP7 occurred within the glycosylation site at aa 70 (leucine to serine), at antigenic region A (aa 96, asparagine to threonine), and at aa 318 (aspartic acid to glycine). It may be speculated that these changes are specific to G4P[6] strains. Furthermore, the observed substitutions may also be particular to South African strains. NSP4, VP8*, and VP7 have been associated with virulence and the amino acid substitutions within these genes correlate with both asymptomatic and symptomatic infection observed in neonates. J. Med. Virol. 62:208–216, 2000. © 2000 Wiley-Liss, Inc.
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