Rotavirus VP7 neutralization epitopes of serotype 3 strains☆
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Cited by (98)
Whole-gene analysis of inter-genogroup reassortant rotaviruses from the Dominican Republic: Emergence of equine-like G3 strains and evidence of their reassortment with locally-circulating strains
2019, VirologyCitation Excerpt :In addition, the shared nt and aa sequence identities among strains were calculated for each gene, using distance matrices prepared using the p-distance algorithm in MEGA6. Lastly, the aa sequences within the VP7 antigenic regions (Ciarlet et al., 1997; Dyall-Smith et al., 1986; Nishikawa et al., 1989) were analyzed using the NCBI-based Amino Acid Explorer online tool (https://www.ncbi.nlm.nih.gov/Class/Structure/aa/aa_explorer.cgi?display=0): aa substitutions were categorized as either ‘conservative’, ‘moderate’, or ‘radical’ by referencing the aa substitution matrix BLOSUM62 (Henikoff and Henikoff, 1992) scores and changes in the resulting aa chemistry (e.g. molecular charge; chemical bonds; the addition/removal of side chains). Of the 49 stool specimens submitted from the DOM to the CDC for genotype identification, 47 were confirmed positive for the detection of RVA and 46 were successfully assigned VP7 and VP4 genotypes using at least two of the molecular assays described previously.
Rotavirus Vaccines
2017, Plotkin's VaccinesIdentification, phylogenetic analysis and classification of porcine group C rotavirus VP7 sequences from the United States and Canada
2013, VirologyCitation Excerpt :The porcine strain 134/04–18 was assigned to the G5 genotype, and porcine strains 344-04-7, 43/06–22, 134/04-2, and 43/06–16 constituted the G6 genotype, while the porcine strain 42/05–21 remained unassigned (Abid et al., 2007; Adah et al., 2002; Araujo et al., 2011; Banyai et al., 2006; Castello et al., 2009; Jiang et al., 1995, 1996; Khamrin et al., 2008, Kuzuya et al., 2007; Martella et al., 2007; Medici et al., 2009; Mitui et al., 2009; Moon et al., 2011; Rahman et al., 2005; Schnagl et al., 2004). Sequencing analyses of the human Ehime (G4PX), bovine Shintoku (G2PX) and porcine Cowden (G1PX), WH (G1PX), and HF (G3PX) RVC strains revealed a minimum of 8 variable regions (VR-1 to VR-8) in the RVC VP7 protein, much like it has been demonstrated for the RVA VP7 protein (Ciarlet et al., 1997; Nishikawa et al., 1989; Tsunemitsu et al., 1992, 1996). To date, several hundred RVA genomes have been completely sequenced (Matthijnssens and Van Ranst, 2012).
Detection of substantial porcine group B rotavirus genetic diversity in the United States, resulting in a modified classification proposal for G genotypes
2012, VirologyCitation Excerpt :Since the amino acid residues, which form the epitopes responsible for the serotypes specificity are currently unknown for VP7 of RVB, it is difficult to speculate on the correlation between RVB VP7 serotypes and genotypes, and future serological assays will have to be performed to study these relationships. However, for the majority of the RVB genotypes, the amino acid identity ranges among RVB strains belonging to the same G genotype is also above the 89% cut-off value (Table 2) as previously determined for RVA strains to discriminate serotypes (Nishikawa et al., 1989). For a few RVB genotypes (G6, G7, G12 and G16) the diversity extends below the 89% amino acid cut-off value, which was also observed for a few RVA G genotypes such as G1–G4 and G6 (Matthijnssens et al., 2008a).
Rotavirus vaccines
2012, Vaccines: Sixth EditionMolecular characterization and analysis of equine rotavirus circulating in Japan from 2003 to 2008
2011, Veterinary MicrobiologyCitation Excerpt :Phylogenetic analysis (Fig. 1) showed that all eight viruses were clustered into the G3B subtype together with other G3 viruses, which have been circulating for a long time in Japan. The amino acid (aa) sequences of VP7 antigenic regions A (aa 87–101), B (aa 141–152), C (aa 208–224) and F (aa 235–242) are aligned in Fig. 2 (Ciarlet et al., 1997; Dyall-Smith et al., 1986; Kobayashi et al., 1991; Nishikawa et al., 1989). The antigenic regions of the eight G3 viruses examined in this study were completely matched.
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Sequence data from this article have been deposited with the EMBL/GenBank Data Libraries under Accession No. J04361.