Steele A D, Parker S P, Peenze I, Pager C T, Taylor M B, Cubitt W D
MRC/MEDUNSA Diarrhoeal Pathogens Research Unit, PO Box 173, Medunsa 0204, Pretoria, South Africa1.
Department of Virology, Camelia Botnar Laboratories, Great Ormond Street Hospital, London, UK2.
J Gen Virol. 1999 Nov;80 ( Pt 11):3029-3034. doi: 10.1099/0022-1317-80-11-3029.
Epidemiological studies on the VP7 serotype prevalence of human rotaviruses in South Africa and the United Kingdom identified several strains which could not be serotyped as G1-G4 by monoclonal antibodies. Further analysis of these strains with a G8-specific monoclonal antibody and with probes for human rotaviruses confirmed them as G8 rotaviruses. These G8 strains exhibited a high degree of sequence identity when compared with each other and with other rotavirus G8 strains. Five South African strains were further characterized as VP6 subgroup I, but with a long RNA electropherotype, which is similar to the G8 strains previously isolated in Finland. In the UK strains, one was VP6 subgroup II with a long RNA electropherotype (similar to the Italian G8 strain). The other two were subgroup I with a short RNA electropherotype. None of these strains exhibited the super-short RNA electropherotype described in the prototype G8 strains recovered from Indonesia (69M).