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Pollens destroy respiratory epithelial cell anchors and drive alphaherpesvirus infection

Pollens are well-known triggers of respiratory allergies and asthma. The pollen burden in today’s ambient air is constantly increasing due to rising climate change and air pollution. How pollens interact with the respiratory mucosa remains largely unknown due to a lack of representative model system...

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Autores principales: Van Cleemput, Jolien, Poelaert, Katrien C. K., Laval, Kathlyn, Impens, Francis, Van den Broeck, Wim, Gevaert, Kris, Nauwynck, Hans. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6423322/
https://www.ncbi.nlm.nih.gov/pubmed/30886217
http://dx.doi.org/10.1038/s41598-019-41305-y
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author Van Cleemput, Jolien
Poelaert, Katrien C. K.
Laval, Kathlyn
Impens, Francis
Van den Broeck, Wim
Gevaert, Kris
Nauwynck, Hans. J.
author_facet Van Cleemput, Jolien
Poelaert, Katrien C. K.
Laval, Kathlyn
Impens, Francis
Van den Broeck, Wim
Gevaert, Kris
Nauwynck, Hans. J.
author_sort Van Cleemput, Jolien
collection PubMed
description Pollens are well-known triggers of respiratory allergies and asthma. The pollen burden in today’s ambient air is constantly increasing due to rising climate change and air pollution. How pollens interact with the respiratory mucosa remains largely unknown due to a lack of representative model systems. We here demonstrate how pollen proteases of Kentucky bluegrass, white birch and hazel selectively destroy integrity and anchorage of columnar respiratory epithelial cells, but not of basal cells, in both ex vivo respiratory mucosal explants and in vitro primary equine respiratory epithelial cells (EREC). In turn, this pollen protease-induced damage to respiratory epithelial cell anchorage resulted in increased infection by the host-specific and ancestral alphaherpesvirus equine herpesvirus type 1 (EHV1). Pollen proteases of all three plant species were characterized by zymography and those of white birch were fully identified for the first time as serine proteases of the subtilase family and meiotic prophase aminopeptidase 1 using mass spectrometry-based proteomics. Together, our findings demonstrate that pollen proteases selectively and irreversibly damage integrity and anchorage of columnar respiratory epithelial cells. In turn, alphaherpesviruses benefit from this partial loss-of-barrier function, resulting in increased infection of the respiratory epithelium.
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spelling pubmed-64233222019-03-26 Pollens destroy respiratory epithelial cell anchors and drive alphaherpesvirus infection Van Cleemput, Jolien Poelaert, Katrien C. K. Laval, Kathlyn Impens, Francis Van den Broeck, Wim Gevaert, Kris Nauwynck, Hans. J. Sci Rep Article Pollens are well-known triggers of respiratory allergies and asthma. The pollen burden in today’s ambient air is constantly increasing due to rising climate change and air pollution. How pollens interact with the respiratory mucosa remains largely unknown due to a lack of representative model systems. We here demonstrate how pollen proteases of Kentucky bluegrass, white birch and hazel selectively destroy integrity and anchorage of columnar respiratory epithelial cells, but not of basal cells, in both ex vivo respiratory mucosal explants and in vitro primary equine respiratory epithelial cells (EREC). In turn, this pollen protease-induced damage to respiratory epithelial cell anchorage resulted in increased infection by the host-specific and ancestral alphaherpesvirus equine herpesvirus type 1 (EHV1). Pollen proteases of all three plant species were characterized by zymography and those of white birch were fully identified for the first time as serine proteases of the subtilase family and meiotic prophase aminopeptidase 1 using mass spectrometry-based proteomics. Together, our findings demonstrate that pollen proteases selectively and irreversibly damage integrity and anchorage of columnar respiratory epithelial cells. In turn, alphaherpesviruses benefit from this partial loss-of-barrier function, resulting in increased infection of the respiratory epithelium. Nature Publishing Group UK 2019-03-18 /pmc/articles/PMC6423322/ /pubmed/30886217 http://dx.doi.org/10.1038/s41598-019-41305-y Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Van Cleemput, Jolien
Poelaert, Katrien C. K.
Laval, Kathlyn
Impens, Francis
Van den Broeck, Wim
Gevaert, Kris
Nauwynck, Hans. J.
Pollens destroy respiratory epithelial cell anchors and drive alphaherpesvirus infection
title Pollens destroy respiratory epithelial cell anchors and drive alphaherpesvirus infection
title_full Pollens destroy respiratory epithelial cell anchors and drive alphaherpesvirus infection
title_fullStr Pollens destroy respiratory epithelial cell anchors and drive alphaherpesvirus infection
title_full_unstemmed Pollens destroy respiratory epithelial cell anchors and drive alphaherpesvirus infection
title_short Pollens destroy respiratory epithelial cell anchors and drive alphaherpesvirus infection
title_sort pollens destroy respiratory epithelial cell anchors and drive alphaherpesvirus infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6423322/
https://www.ncbi.nlm.nih.gov/pubmed/30886217
http://dx.doi.org/10.1038/s41598-019-41305-y
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