Elsevier

Virology

Volume 171, Issue 2, August 1989, Pages 503-515
Virology

Rotavirus VP7 neutralization epitopes of serotype 3 strains

https://doi.org/10.1016/0042-6822(89)90620-XGet rights and content

Abstract

Sequence analysis of the gene encoding the major neutralization glycoprotein (VP7) was performed on 27 human and animal rotavirus strains of serotype 3 in order to examine genetic variation within srains of identical serotype. Comparisons of the deduced amino acid sequences of the VP7s showed overall sequence identities of 85% or higher. A higher degree of overall VP7 sequence similarity was observed among strains from the same animal species when compared to strains from different animal species, suggesting that there are species-specific sequences in the VP7 protein. Alignment of the amino acid sequences demonstrated that amino acid sequence divergence among serotype 3 strains from different species was located primarily in previously established VP7 serotype-specific regions where genetic variation was identified among strains of different serotype. These regions were highly conserved among serotype 3 strains derived from the same species. The varying reactivities of three anti-VP7 monoclonal antibodies with the 27 strains was consistent with the occurrence of antigenic variation among serotype 3 strains. Moreover the reactivity of monoclonal antibodies correlated with the amino acid sequence found in two serotype-specific regions (VR5 and VR8). A computer-derived predicted phylogenetic tree suggests that rotavirus strains from different animal species belonging to serotype 3 are more closely related to each other than to rotavirus strains of different serotypes.

References (54)

  • C. Ward et al.

    The Hong Kong hemagglutinin. Structural relationships between the human (H3) hemagglutinins and the hemagglutinin from the putative progenitor strain A/Duck/Ukraine/1/63 (HAV7)

  • L.M. Bell et al.

    Gastroenteritis caused by human rotaviruses (serotype three) in a suckling mouse model

  • D.A. Benfield et al.

    A monoclonal antibody to the Gottfried strain of porcine rotavirus which neutralizes rotavirus serotype 3, 4, and 6

  • C.J. Birch et al.

    Isolation of feline rotaviruses and their relationship to human and simian isolates by electropherotype and serotype

    J. Gen. Virol.

    (1985)
  • J. Caust et al.

    Glycosylation, an important modifier of rotavirus antigenicity

    Arch. Virol.

    (1987)
  • H.F. Clark et al.

    Protective effect of WC3 vaccine against rotavirus diarrhea in infants during a predominantly serotype 1 rotavirus season

    J. Infect. Dis.

    (1988)
  • H.F. Clark et al.

    Rotavirus isolate WI61 representing a presumptive new human serotype

    J. Clin. Microbiol.

    (1987)
  • M.L. Dyall-Smith et al.

    Location of the major antigenic sites involved in rotavirus serotype-specific neutralization

  • W.M. Fitch et al.

    Construction of phylogenetic trees

    Science

    (1967)
  • J. Flores et al.

    In vitro transcription of two human rotaviruses

    J. Virol.

    (1982)
  • M. Gorziglia et al.

    VP7 serotype-specific glycoprotein of OSU porcine rotavirus: Coding assignment and gene sequence

    J. Gen. Virol.

    (1986)
  • M. Gorziglia et al.

    Conservation of amino acid sequence of VP8 and cleavage region of 84-kDa outer capsid protein among rotaviruses recovered from asymptomatic neonatal infection

  • H.B. Greenberg et al.

    Gene coding assignments for growth restriction, neutralization and subgroup specificities of the W and DS-1 strains of human rotavirus

    J. Gen. Virol.

    (1983)
  • H.B. Greenberg et al.

    Production and preliminary characterization of monoclonal antibodies directed at two surface proteins of rhesus rotavirus

    J. Virol.

    (1983)
  • H.B. Greenberg et al.

    Cultivation and characterization of three strains of murine rotavirus

    J. Virol.

    (1986)
  • H.B. Greenberg et al.

    Rescue and serotypic characterization of noncultivable human rotavirus by gene reassortment

    Infect. Immun.

    (1982)
  • Y. Hoshino et al.

    Serotypic similarity and diversity of rotaviruses of mammalian and avian origin as studied by plaque-reduction neutralization

    J. Infect. Dis.

    (1984)
  • 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, Virology
      Citation 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 Vaccines
    • Identification, phylogenetic analysis and classification of porcine group C rotavirus VP7 sequences from the United States and Canada

      2013, Virology
      Citation 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, Virology
      Citation 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 Edition
    • Molecular characterization and analysis of equine rotavirus circulating in Japan from 2003 to 2008

      2011, Veterinary Microbiology
      Citation 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.

    View all citing articles on Scopus

    Sequence data from this article have been deposited with the EMBL/GenBank Data Libraries under Accession No. J04361.

    View full text