Group C rotavirus (GCRV) is distributed worldwide as an enteric pathogen in humans and animals. However, to date, whole-genome sequences are available only for a human strain (Bristol) and a porcine strain (Cowden). To investigate the genetic diversity of human GCRVs, nearly full-length sequences of all 11 RNA segments were determined for human GCRVs detected recently in India (v508), Bangladesh (BS347), China (Wu82 and YNR001) and Japan (OH567 and BK0830) and analysed phylogenetically with sequence data for GCRVs published previously. All the RNA segments of human GCRV strains except for the VP3 gene showed high levels of conservation (.93 % nucleotide sequence identity, .92 % amino acid sequence identity), belonging to a single genetic cluster distinct from those of animal GCRVs. In contrast, the VP3 genes of human GCRVs could be discriminated into two clusters, designated M2 and M3, that were distinguished phylogenetically from those of porcine and bovine GCRVs (clusters M1 and M4, respectively). Between M2 and M3, amino acid sequence identity of the VP3 gene was 84.1-84.7 %, whereas high identities were observed within each cluster (92.3-97.6 % for M2, 98.2-99.3 % for M3). Sequence divergence among the four VP3 clusters was observed throughout the amino acid sequence except for conserved motifs, including those possibly related to enzyme functions of VP3. The presence of obvious genetic diversity only in the VP3 gene among human GCRVs suggested that either the M2 or M3 VP3 gene of human GCRVs might have been derived through reassortment from an animal GCRV or from an unidentified human GCRV strain belonging to a novel genogroup.
INTRODUCTIONRotavirus, a member of the family Reoviridae, is the most important viral pathogen that causes gastroenteritis in humans. The rotavirus genome consists of 11 segments of dsRNA, and the viral particle is composed of three concentric layers, the outer capsid, inner capsid and core (Estes & Kapikian, 2007). The outer capsid consists of two structural proteins, VP4 and VP7, which contain neutralization antigens. The inner capsid consists of structural protein VP6. Rotavirus is classified into seven groups, A-G, based on the antigenicity of the inner capsid protein VP6 and genomic characteristics (Kapikian et al., 2001). In humans, groups A, B and C have been detected to date. Group A rotavirus (GARV) is the most prevalent throughout the world and is recognized as the leading viral pathogen of acute gastroenteritis in children. For epidemiological investigations of GARV, a genetic classification system based on the outer capsid proteins VP7 (G type) and VP4 (P type) has been adopted (Santos & Hoshino, 2005). In addition, a full-genome-based genotyping system composed of genotypes of the 11 individual RNA segments has been proposed on the basis of full-The GenBank/EMBL/DDBJ accession numbers for the GCRV sequences determined in this study are HQ185629-HQ185631 (v508), HQ185632-HQ185642 (BS347), HQ185643-HQ185651 (Wu82), HQ185652-HQ185662 (YNR001), HQ185663-HQ185672 (OH567) and ...