Mapping the hemagglutination domain of rotaviruses
- PMID: 7884915
- PMCID: PMC188943
- DOI: 10.1128/JVI.69.4.2629-2632.1995
Mapping the hemagglutination domain of rotaviruses
Abstract
Most strains of animal rotaviruses are able to agglutinate erythrocytes, and the surface protein VP4 is the virus hemagglutinin. To map the hemagglutination domain on VP4 while preserving the conformation of the protein, we constructed full-length chimeras between the VP4 genes of hemagglutinating (YM) and nonhemagglutinating (KU) rotavirus strains. The parental and chimeric genes were expressed in insect cells, and the recombinant VP4 proteins were evaluated for their capacity to agglutinate human type O erythrocytes. Three chimeric genes, encoding amino acids 1 to 208 (QKU), 93 to 208 (QC), and 93 to 776 (QYM) of the YM VP4 protein in a KU VP4 background, were constructed. YM VP4 and chimeras QKU and QC were shown to specifically hemagglutinate, indicating that the region between amino acids 93 and 208 of YM VP4 is sufficient to determine the hemagglutination activity of the protein.
Similar articles
-
The rhesus rotavirus outer capsid protein VP4 functions as a hemagglutinin and is antigenically conserved when expressed by a baculovirus recombinant.J Virol. 1989 Apr;63(4):1661-8. doi: 10.1128/JVI.63.4.1661-1668.1989. J Virol. 1989. PMID: 2538649 Free PMC article.
-
Antigenic relationships among human rotaviruses as determined by outer capsid protein VP4.Proc Natl Acad Sci U S A. 1990 Sep;87(18):7155-9. doi: 10.1073/pnas.87.18.7155. Proc Natl Acad Sci U S A. 1990. PMID: 1698292 Free PMC article.
-
The amino-terminal half of rotavirus SA114fM VP4 protein contains a hemagglutination domain and primes for neutralizing antibodies to the virus.J Virol. 1991 Mar;65(3):1383-91. doi: 10.1128/JVI.65.3.1383-1391.1991. J Virol. 1991. PMID: 1847459 Free PMC article.
-
Haemagglutination by rotaviruses in relation to VP4 genotypes.Res Virol. 1995 Sep-Oct;146(5):371-4. doi: 10.1016/0923-2516(96)80600-5. Res Virol. 1995. PMID: 8578011 No abstract available.
-
The VP8 fragment of VP4 is the rhesus rotavirus hemagglutinin.Virology. 1991 Apr;181(2):553-63. doi: 10.1016/0042-6822(91)90888-i. Virology. 1991. PMID: 1849677
Cited by
-
Characterization of the interaction between VP8 of bovine rotavirus C486 and cellular components on MA-104 cells and erythrocytes.Can J Vet Res. 1998 Jan;62(1):56-62. Can J Vet Res. 1998. PMID: 9442941 Free PMC article.
-
Gangliosides have a functional role during rotavirus cell entry.J Virol. 2013 Jan;87(2):1115-22. doi: 10.1128/JVI.01964-12. Epub 2012 Nov 7. J Virol. 2013. PMID: 23135722 Free PMC article.
-
Proteolysis of monomeric recombinant rotavirus VP4 yields an oligomeric VP5* core.J Virol. 2001 Aug;75(16):7339-50. doi: 10.1128/JVI.75.16.7339-7350.2001. J Virol. 2001. PMID: 11462006 Free PMC article.
-
Sialic acids in molecular and cellular interactions.Int Rev Cytol. 1997;175:137-240. doi: 10.1016/s0074-7696(08)62127-0. Int Rev Cytol. 1997. PMID: 9203358 Free PMC article. Review.
-
Evolutionary changes between pre- and post-vaccine South African group A G2P[4] rotavirus strains, 2003-2017.Microb Genom. 2022 Apr;8(4):000809. doi: 10.1099/mgen.0.000809. Microb Genom. 2022. PMID: 35446251 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources