Abstract
Between April and December 1993, we determined P and G genotypes of group A rotavirus strains obtained from children admitted to diarrhea treatment centers in five Indian cities. From a total of 63 rotavirus-positive specimens, we identified 10 different strains with five different G genotypes and four distinct P types by using reverse transcription-PCR. The common worldwide strains G1P8, G2P4, G3P8, and G4P8 were underrepresented among Indian children (33%), whereas strains of P type 6 (G1P6, G2P6, G3P6, G4P6, and G9P6), which primarily infect asymptomatic newborns but are rare in children with diarrhea were common in India (43%). Of these, G9P6, a strain not previously reported to be found in children with diarrhea, was the most prevalent (22%). Eleven percent of the strains were nontypeable, and another 11% of the specimens had mixed infections. Using digoxigenin-labeled, genotype-specific hybridization probes, we confirmed all G9 strains and mixed infections tested and identified three nontypeable strains (one G9 and two P8). The epidemiological significance of G9 rotavirus strains, if confirmed in other settings, may have important implications for vaccine development.
Full Text
The Full Text of this article is available as a PDF (286.8 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Ando T., Monroe S. S., Gentsch J. R., Jin Q., Lewis D. C., Glass R. I. Detection and differentiation of antigenically distinct small round-structured viruses (Norwalk-like viruses) by reverse transcription-PCR and southern hybridization. J Clin Microbiol. 1995 Jan;33(1):64–71. doi: 10.1128/jcm.33.1.64-71.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Beards G. M., Desselberger U., Flewett T. H. Temporal and geographical distributions of human rotavirus serotypes, 1983 to 1988. J Clin Microbiol. 1989 Dec;27(12):2827–2833. doi: 10.1128/jcm.27.12.2827-2833.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bern C., Unicomb L., Gentsch J. R., Banul N., Yunus M., Sack R. B., Glass R. I. Rotavirus diarrhea in Bangladeshi children: correlation of disease severity with serotypes. J Clin Microbiol. 1992 Dec;30(12):3234–3238. doi: 10.1128/jcm.30.12.3234-3238.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bishop R. F., Unicomb L. E., Barnes G. L. Epidemiology of rotavirus serotypes in Melbourne, Australia, from 1973 to 1989. J Clin Microbiol. 1991 May;29(5):862–868. doi: 10.1128/jcm.29.5.862-868.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cicirello H. G., Das B. K., Gupta A., Bhan M. K., Gentsch J. R., Kumar R., Glass R. I. High prevalence of rotavirus infection among neonates born at hospitals in Delhi, India: predisposition of newborns for infection with unusual rotavirus. Pediatr Infect Dis J. 1994 Aug;13(8):720–724. doi: 10.1097/00006454-199408000-00008. [DOI] [PubMed] [Google Scholar]
- Das B. K., Gentsch J. R., Cicirello H. G., Woods P. A., Gupta A., Ramachandran M., Kumar R., Bhan M. K., Glass R. I. Characterization of rotavirus strains from newborns in New Delhi, India. J Clin Microbiol. 1994 Jul;32(7):1820–1822. doi: 10.1128/jcm.32.7.1820-1822.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Devereux J., Haeberli P., Smithies O. A comprehensive set of sequence analysis programs for the VAX. Nucleic Acids Res. 1984 Jan 11;12(1 Pt 1):387–395. doi: 10.1093/nar/12.1part1.387. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Estes M. K., Cohen J. Rotavirus gene structure and function. Microbiol Rev. 1989 Dec;53(4):410–449. doi: 10.1128/mr.53.4.410-449.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gentsch J. R., Glass R. I., Woods P., Gouvea V., Gorziglia M., Flores J., Das B. K., Bhan M. K. Identification of group A rotavirus gene 4 types by polymerase chain reaction. J Clin Microbiol. 1992 Jun;30(6):1365–1373. doi: 10.1128/jcm.30.6.1365-1373.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Glass R. I., Keith J., Nakagomi O., Nakagomi T., Askaa J., Kapikian A. Z., Chanock R. M., Flores J. Nucleotide sequence of the structural glycoprotein VP7 gene of Nebraska calf diarrhea virus rotavirus: comparison with homologous genes from four strains of human and animal rotaviruses. Virology. 1985 Mar;141(2):292–298. doi: 10.1016/0042-6822(85)90260-0. [DOI] [PubMed] [Google Scholar]
- Rasool N. B., Larralde G., Gorziglia M. I. Determination of human rotavirus VP4 using serotype-specific cDNA probes. Arch Virol. 1993;133(3-4):275–282. doi: 10.1007/BF01313768. [DOI] [PubMed] [Google Scholar]
- Santos N., Riepenhoff-Talty M., Clark H. F., Offit P., Gouvea V. VP4 genotyping of human rotavirus in the United States. J Clin Microbiol. 1994 Jan;32(1):205–208. doi: 10.1128/jcm.32.1.205-208.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Silberstein I., Shulman L. M., Mendelson E., Shif I. Distribution of both rotavirus VP4 genotypes and VP7 serotypes among hospitalized and nonhospitalized Israeli children. J Clin Microbiol. 1995 May;33(5):1421–1422. doi: 10.1128/jcm.33.5.1421-1422.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Steele A. D., van Niekerk M. C., Mphahlele M. J. Geographic distribution of human rotavirus VP4 genotypes and VP7 serotypes in five South African regions. J Clin Microbiol. 1995 Jun;33(6):1516–1519. doi: 10.1128/jcm.33.6.1516-1519.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Timenetsky M. do C., Santos N., Gouvea V. Survey of rotavirus G and P types associated with human gastroenteritis in São Paulo, Brazil, from 1986 to 1992. J Clin Microbiol. 1994 Oct;32(10):2622–2624. doi: 10.1128/jcm.32.10.2622-2624.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Woods P. A., Gentsch J., Gouvea V., Mata L., Santosham M., Bai Z. S., Urasawa S., Glass R. I. Distribution of serotypes of human rotavirus in different populations. J Clin Microbiol. 1992 Apr;30(4):781–785. doi: 10.1128/jcm.30.4.781-785.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]