Three rare human G12 strains were detected from diarrheic clinical samples of children (<8 months of age) in Calcutta during a routine surveillance study of rotaviral diarrhea in India. The VP7 genes of G12 strains and their products showed maximum homology (97 to 99% at the nucleotide level and 98% at the amino acid level, respectively) with those of two recently reported G12 strains (from the United States and Thailand) but lesser homology with those of prototype G12 strain L26.Rotaviruses are the major cause of acute gastroenteritis in infants and young of a wide variety of mammalian and avian species (11). In developing countries, approximately 130 million infants are infected with rotaviruses and there are 800,000 annual deaths (5, 12). In group A rotaviruses, 15 VP7 G serotypes and 21 VP4 P genotypes have been reported for humans, animals, and birds (17). Though 10 G types and 10 P types from humans have been reported (15), clinically and epidemiologically the most important strains belong to the G1 to G4 serotypes with P[8] and P[4] genotypes (6,14). On the other hand, some unusual types (G5, G8, and G9) and rare combinations of G and P types from different countries have also been reported (1,2,3,4,13,16,20). The human rotavirus G12 strains (L26 and L27) were first detected from Philippines in 1990 (19). After more than a decade, in 2002, human G12 strains Se585 (9) and T152 (15) from the United States and Thailand, respectively, were reported. In this study, we report the detection of three rare G12 strains of human rotaviruses in India.As part of a routine surveillance study for diarrheal diseases, stool samples were collected from children below 4 years of age from B. C. Roy Children's Hospital and also from patients of all age groups admitted to the Infectious Diseases Hospital, Calcutta, India, in 2001. Stool samples were also collected from children with diarrhea from Assam Medical College, Dibrugarh, Assam, India; Capital Hospital and Municipality Hospital, Bhubaneshwar, Orissa, eastern India; and Post-Graduate Institute of Medical Education and Research, Chandigarh, northern India. A total of 454 samples were screened for rotaviruses by RNA electrophoresis as described earlier by Herring et al. (10). The fecal specimens were processed for extraction of rotavirus double-stranded RNA suitable for reverse transcription and amplification of the VP4 and VP7 genes as described previously (4). G and P typing of positive samples was carried out by nested and multiplex PCR with consensus and type-specific primers as described previously (4,7,8,18,21). The amplified products were purified with either the QIAquick gel extraction kit or the PCR purification kit (Qiagen, GmBH) in accordance with the manufacturer's instructions. Direct sequencing was carried out by using ABI PRISM BigDye terminator cycle sequencing kits (Applied Biosystems) with an automated DNA sequencer, the ABI PRISM 310 genetic analyzer (Applied Biosystems). The sequencing of the VP7 genes of all three isolates was repeated three times to...