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Mechanism of human rhinovirus infections
About 150 human rhinovirus serotypes are responsible for more than 50 % of recurrent upper respiratory infections. Despite having similar 3D structures, some bind members of the low-density lipoprotein receptor family, some ICAM-1, and some use CDHR3 for host cell infection. This is also reflected i...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4889530/ https://www.ncbi.nlm.nih.gov/pubmed/27251607 http://dx.doi.org/10.1186/s40348-016-0049-3 |
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author | Blaas, Dieter Fuchs, Renate |
author_facet | Blaas, Dieter Fuchs, Renate |
author_sort | Blaas, Dieter |
collection | PubMed |
description | About 150 human rhinovirus serotypes are responsible for more than 50 % of recurrent upper respiratory infections. Despite having similar 3D structures, some bind members of the low-density lipoprotein receptor family, some ICAM-1, and some use CDHR3 for host cell infection. This is also reflected in the pathways exploited for cellular entry. We found that even rhinovirus serotypes binding the same receptor can travel along different endocytic pathways and release their RNA genome into the cytosol at different locations. How this may account for distinct immune responses elicited by various rhinoviruses and the observed symptoms of the common cold is briefly discussed. |
format | Online Article Text |
id | pubmed-4889530 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-48895302016-06-17 Mechanism of human rhinovirus infections Blaas, Dieter Fuchs, Renate Mol Cell Pediatr Mini Review About 150 human rhinovirus serotypes are responsible for more than 50 % of recurrent upper respiratory infections. Despite having similar 3D structures, some bind members of the low-density lipoprotein receptor family, some ICAM-1, and some use CDHR3 for host cell infection. This is also reflected in the pathways exploited for cellular entry. We found that even rhinovirus serotypes binding the same receptor can travel along different endocytic pathways and release their RNA genome into the cytosol at different locations. How this may account for distinct immune responses elicited by various rhinoviruses and the observed symptoms of the common cold is briefly discussed. Springer Berlin Heidelberg 2016-06-01 /pmc/articles/PMC4889530/ /pubmed/27251607 http://dx.doi.org/10.1186/s40348-016-0049-3 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Mini Review Blaas, Dieter Fuchs, Renate Mechanism of human rhinovirus infections |
title | Mechanism of human rhinovirus infections |
title_full | Mechanism of human rhinovirus infections |
title_fullStr | Mechanism of human rhinovirus infections |
title_full_unstemmed | Mechanism of human rhinovirus infections |
title_short | Mechanism of human rhinovirus infections |
title_sort | mechanism of human rhinovirus infections |
topic | Mini Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4889530/ https://www.ncbi.nlm.nih.gov/pubmed/27251607 http://dx.doi.org/10.1186/s40348-016-0049-3 |
work_keys_str_mv | AT blaasdieter mechanismofhumanrhinovirusinfections AT fuchsrenate mechanismofhumanrhinovirusinfections |