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Infection of polarized bovine respiratory epithelial cells by bovine viral diarrhea virus (BVDV)

Bovine viral diarrhea virus (BVDV) is affecting cattle populations all over the world causing acute disease, immunosuppressive effects, respiratory diseases, gastrointestinal, and reproductive failure in cattle. The virus is taken up via the oronasal route and infection of epithelial and immune cell...

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Autores principales: Su, Ang, Fu, Yuguang, Meens, Jochen, Yang, Wei, Meng, Fandan, Herrler, Georg, Becher, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801128/
https://www.ncbi.nlm.nih.gov/pubmed/33300445
http://dx.doi.org/10.1080/21505594.2020.1854539
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author Su, Ang
Fu, Yuguang
Meens, Jochen
Yang, Wei
Meng, Fandan
Herrler, Georg
Becher, Paul
author_facet Su, Ang
Fu, Yuguang
Meens, Jochen
Yang, Wei
Meng, Fandan
Herrler, Georg
Becher, Paul
author_sort Su, Ang
collection PubMed
description Bovine viral diarrhea virus (BVDV) is affecting cattle populations all over the world causing acute disease, immunosuppressive effects, respiratory diseases, gastrointestinal, and reproductive failure in cattle. The virus is taken up via the oronasal route and infection of epithelial and immune cells contributes to the dissemination of the virus throughout the body. However, it is not known how the virus gets across the barrier of epithelial cells encountered in the airways. Here, we analyzed the infection of polarized primary bovine airway epithelial cells (BAEC). Infection of BAEC by a non-cytopathogenic BVDV was possible via both the apical and the basolateral plasma membrane, but the infection was most efficient when the virus was applied to the basolateral plasma membrane. Irrespective of the site of infection, BVDV was efficiently released to the apical site, while only minor amounts of virus were detected in the basal medium. This indicates that the respiratory epithelium can release large amounts of BVDV to the environment and susceptible animals via respiratory fluids and aerosols, but BVDV cannot cross the airway epithelial cells to infect subepithelial cells and establish systemic infection. Further experiments showed that the receptor, bovine CD46, for BVDV is expressed predominantly on the apical membrane domain of the polarized epithelial cells. In a CD46 blocking experiment, the addition of an antibody directed against CD46 almost completely inhibited apical infection, whereas basolateral infection was not affected. While CD46 serves as a receptor for apical infection of BAEC by BVDV, the receptor for basolateral infection remains to be elucidated.
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spelling pubmed-78011282021-01-21 Infection of polarized bovine respiratory epithelial cells by bovine viral diarrhea virus (BVDV) Su, Ang Fu, Yuguang Meens, Jochen Yang, Wei Meng, Fandan Herrler, Georg Becher, Paul Virulence Research Paper Bovine viral diarrhea virus (BVDV) is affecting cattle populations all over the world causing acute disease, immunosuppressive effects, respiratory diseases, gastrointestinal, and reproductive failure in cattle. The virus is taken up via the oronasal route and infection of epithelial and immune cells contributes to the dissemination of the virus throughout the body. However, it is not known how the virus gets across the barrier of epithelial cells encountered in the airways. Here, we analyzed the infection of polarized primary bovine airway epithelial cells (BAEC). Infection of BAEC by a non-cytopathogenic BVDV was possible via both the apical and the basolateral plasma membrane, but the infection was most efficient when the virus was applied to the basolateral plasma membrane. Irrespective of the site of infection, BVDV was efficiently released to the apical site, while only minor amounts of virus were detected in the basal medium. This indicates that the respiratory epithelium can release large amounts of BVDV to the environment and susceptible animals via respiratory fluids and aerosols, but BVDV cannot cross the airway epithelial cells to infect subepithelial cells and establish systemic infection. Further experiments showed that the receptor, bovine CD46, for BVDV is expressed predominantly on the apical membrane domain of the polarized epithelial cells. In a CD46 blocking experiment, the addition of an antibody directed against CD46 almost completely inhibited apical infection, whereas basolateral infection was not affected. While CD46 serves as a receptor for apical infection of BAEC by BVDV, the receptor for basolateral infection remains to be elucidated. Taylor & Francis 2021-01-04 /pmc/articles/PMC7801128/ /pubmed/33300445 http://dx.doi.org/10.1080/21505594.2020.1854539 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Su, Ang
Fu, Yuguang
Meens, Jochen
Yang, Wei
Meng, Fandan
Herrler, Georg
Becher, Paul
Infection of polarized bovine respiratory epithelial cells by bovine viral diarrhea virus (BVDV)
title Infection of polarized bovine respiratory epithelial cells by bovine viral diarrhea virus (BVDV)
title_full Infection of polarized bovine respiratory epithelial cells by bovine viral diarrhea virus (BVDV)
title_fullStr Infection of polarized bovine respiratory epithelial cells by bovine viral diarrhea virus (BVDV)
title_full_unstemmed Infection of polarized bovine respiratory epithelial cells by bovine viral diarrhea virus (BVDV)
title_short Infection of polarized bovine respiratory epithelial cells by bovine viral diarrhea virus (BVDV)
title_sort infection of polarized bovine respiratory epithelial cells by bovine viral diarrhea virus (bvdv)
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7801128/
https://www.ncbi.nlm.nih.gov/pubmed/33300445
http://dx.doi.org/10.1080/21505594.2020.1854539
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