Molecular characterization of serotype G2 and G3 human rotavirus strains that have an apparently identical electropherotype of the short RNA pattern

Archives of Virology - Tập 147 - Trang 2187-2195 - 2002
T. Nakagomi1, J. R. Gentsch2, B. K. Das3, R. Kumar3, M. K. Bhan3, R. I. Glass2, O. Nakagomi1
1Department of Microbiology, Akita University School of Medicine, Akita, Japan, , JP
2Division of Viral and Rickettsial Diseases, Center for Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, U.S.A., , US
3Departments of Pediatrics and Microbiology, Division of Gastroenterology and Enteric Infections, All India Institute of Medical Sciences, New Delhi, India, , IN

Tóm tắt

 The literature is conflicting whether or not rotavirus strains with different G serotype have an identical electropherotype. This is a contentious but an important issue because large parts of molecular epidemiological studies of rotaviruses have been based on the conception that a single strain of rotavirus can be defined by a single electropherotype. Here, we examined in detail by reverse-transcription PCR genotyping, electropherotyping, sequencing, and genogrouping using RNA--RNA hybridization three human rotavirus strains isolated in India that had apparently identical electropherotypes although one strain was typed as P[4], G3 while the other two typed as P[4], G2. These three strains showed an identical electropherotype on 7.5% and 12.5% polyacrylamide gels, but co-electrophoresis on a 10% gel demonstrated that segment 8 of the P[4], G3 strain migrated more slowly than the cognate segment of the P[4], G2 strains. Genogrouping assay and nucleotide sequencing provided evidence for the hypothesis that the P[4], G3 stain was an intergenogroup reassortant in which a P[4], G2 strain of the DS-1 genogroup had acquired the VP7 gene from an yet-unidentified concurrently circulating G3 strain. While electropherotyping remains a valuable asset for molecular epidemiology of rotaviruses, this study underscores the importance of co-electrophoresis under different electrophoretic conditions when pinpointing subtle differences.