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Antigenic Diversity of Human Sapoviruses
Sapovirus (SaV) is a causative agent of gastroenteritis. On the basis of capsid protein (VP1) nucleotide sequences, SaV can be divided into 5 genogroups (GI–GV), of which the GI, GII, GIV, and GV strains infect humans. SaV is uncultivable, but expression of recombinant VP1 in insect cells results in...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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Centers for Disease Control and Prevention
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2851512/ https://www.ncbi.nlm.nih.gov/pubmed/18258001 http://dx.doi.org/10.3201/eid1310.070402 |
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author | Hansman, Grant S. Oka, Tomoichiro Sakon, Naomi Takeda, Naokazu |
author_facet | Hansman, Grant S. Oka, Tomoichiro Sakon, Naomi Takeda, Naokazu |
author_sort | Hansman, Grant S. |
collection | PubMed |
description | Sapovirus (SaV) is a causative agent of gastroenteritis. On the basis of capsid protein (VP1) nucleotide sequences, SaV can be divided into 5 genogroups (GI–GV), of which the GI, GII, GIV, and GV strains infect humans. SaV is uncultivable, but expression of recombinant VP1 in insect cells results in formation of viruslike particles (VLPs) that are antigenically similar to native SaV. In this study, we newly expressed SaV GII and GIV VLPs to compare genetic and antigenic relationships among all human SaV genogroups. Hyperimmune antiserum samples against VLPs reacted strongly with homologous VLPs. However, several antiserum samples weakly cross-reacted against heterologous VLPs in an antibody ELISA. Conversely, an antigen ELISA showed that VLPs of SaV in all human genogroups were antigenically distinct. These findings indicate a likely correspondence between SaV antigenicity and VP1 genogrouping and genotyping. |
format | Text |
id | pubmed-2851512 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Centers for Disease Control and Prevention |
record_format | MEDLINE/PubMed |
spelling | pubmed-28515122010-04-15 Antigenic Diversity of Human Sapoviruses Hansman, Grant S. Oka, Tomoichiro Sakon, Naomi Takeda, Naokazu Emerg Infect Dis Research Sapovirus (SaV) is a causative agent of gastroenteritis. On the basis of capsid protein (VP1) nucleotide sequences, SaV can be divided into 5 genogroups (GI–GV), of which the GI, GII, GIV, and GV strains infect humans. SaV is uncultivable, but expression of recombinant VP1 in insect cells results in formation of viruslike particles (VLPs) that are antigenically similar to native SaV. In this study, we newly expressed SaV GII and GIV VLPs to compare genetic and antigenic relationships among all human SaV genogroups. Hyperimmune antiserum samples against VLPs reacted strongly with homologous VLPs. However, several antiserum samples weakly cross-reacted against heterologous VLPs in an antibody ELISA. Conversely, an antigen ELISA showed that VLPs of SaV in all human genogroups were antigenically distinct. These findings indicate a likely correspondence between SaV antigenicity and VP1 genogrouping and genotyping. Centers for Disease Control and Prevention 2007-10 /pmc/articles/PMC2851512/ /pubmed/18258001 http://dx.doi.org/10.3201/eid1310.070402 Text en https://creativecommons.org/licenses/by/4.0/This is a publication of the U.S. Government. This publication is in the public domain and is therefore without copyright. All text from this work may be reprinted freely. Use of these materials should be properly cited. |
spellingShingle | Research Hansman, Grant S. Oka, Tomoichiro Sakon, Naomi Takeda, Naokazu Antigenic Diversity of Human Sapoviruses |
title | Antigenic Diversity of Human Sapoviruses |
title_full | Antigenic Diversity of Human Sapoviruses |
title_fullStr | Antigenic Diversity of Human Sapoviruses |
title_full_unstemmed | Antigenic Diversity of Human Sapoviruses |
title_short | Antigenic Diversity of Human Sapoviruses |
title_sort | antigenic diversity of human sapoviruses |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2851512/ https://www.ncbi.nlm.nih.gov/pubmed/18258001 http://dx.doi.org/10.3201/eid1310.070402 |
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