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Norovirus Binding to Ligands Beyond Histo-Blood Group Antigens

Histo-blood group antigens (HBGAs) are commonly accepted as the cellular receptors for human norovirus. However, some human noroviruses have been found not to bind any HBGA ligand, suggesting potential additional co-factors. Some ligands have been found to bind noroviruses and have the potential to...

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Autores principales: Almand, Erin A., Moore, Matthew D., Jaykus, Lee-Ann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5742575/
https://www.ncbi.nlm.nih.gov/pubmed/29312233
http://dx.doi.org/10.3389/fmicb.2017.02549
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author Almand, Erin A.
Moore, Matthew D.
Jaykus, Lee-Ann
author_facet Almand, Erin A.
Moore, Matthew D.
Jaykus, Lee-Ann
author_sort Almand, Erin A.
collection PubMed
description Histo-blood group antigens (HBGAs) are commonly accepted as the cellular receptors for human norovirus. However, some human noroviruses have been found not to bind any HBGA ligand, suggesting potential additional co-factors. Some ligands have been found to bind noroviruses and have the potential to be additional cellular receptors/attachment factors for human norovirus or inhibitors of the HBGA interaction. The studies identifying these mostly characterize different chemical, human, food, or bacterial components and their effect on norovirus binding and infection, although the mechanism of interaction is unknown in many cases. This review seeks to supplement the already well-covered HBGA-norovirus literature by covering non-HBGA human norovirus ligands and inhibitors to provide investigators with a more comprehensive view of norovirus ligands.
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spelling pubmed-57425752018-01-08 Norovirus Binding to Ligands Beyond Histo-Blood Group Antigens Almand, Erin A. Moore, Matthew D. Jaykus, Lee-Ann Front Microbiol Microbiology Histo-blood group antigens (HBGAs) are commonly accepted as the cellular receptors for human norovirus. However, some human noroviruses have been found not to bind any HBGA ligand, suggesting potential additional co-factors. Some ligands have been found to bind noroviruses and have the potential to be additional cellular receptors/attachment factors for human norovirus or inhibitors of the HBGA interaction. The studies identifying these mostly characterize different chemical, human, food, or bacterial components and their effect on norovirus binding and infection, although the mechanism of interaction is unknown in many cases. This review seeks to supplement the already well-covered HBGA-norovirus literature by covering non-HBGA human norovirus ligands and inhibitors to provide investigators with a more comprehensive view of norovirus ligands. Frontiers Media S.A. 2017-12-21 /pmc/articles/PMC5742575/ /pubmed/29312233 http://dx.doi.org/10.3389/fmicb.2017.02549 Text en Copyright © 2017 Almand, Moore and Jaykus. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Almand, Erin A.
Moore, Matthew D.
Jaykus, Lee-Ann
Norovirus Binding to Ligands Beyond Histo-Blood Group Antigens
title Norovirus Binding to Ligands Beyond Histo-Blood Group Antigens
title_full Norovirus Binding to Ligands Beyond Histo-Blood Group Antigens
title_fullStr Norovirus Binding to Ligands Beyond Histo-Blood Group Antigens
title_full_unstemmed Norovirus Binding to Ligands Beyond Histo-Blood Group Antigens
title_short Norovirus Binding to Ligands Beyond Histo-Blood Group Antigens
title_sort norovirus binding to ligands beyond histo-blood group antigens
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5742575/
https://www.ncbi.nlm.nih.gov/pubmed/29312233
http://dx.doi.org/10.3389/fmicb.2017.02549
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