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Adenylate cyclase toxin of Bordetella parapertussis disrupts the epithelial barrier granting the bacterial access to the intracellular space of epithelial cells
B. parapertussis is one of the etiological agents of whooping cough. Once inhaled, the bacteria bind to the respiratory epithelium and start the infection. Little is known about this first step of host colonization and the role of the human airway epithelial barrier on B. parapertussis infection. We...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10681170/ https://www.ncbi.nlm.nih.gov/pubmed/38011105 http://dx.doi.org/10.1371/journal.pone.0291331 |
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author | Gorgojo, Juan Pablo Carrica, Mariela del Carmen Baroli, Carlos Manuel Valdez, Hugo Alberto Alvarez Hayes, Jimena Rodriguez, Maria Eugenia |
author_facet | Gorgojo, Juan Pablo Carrica, Mariela del Carmen Baroli, Carlos Manuel Valdez, Hugo Alberto Alvarez Hayes, Jimena Rodriguez, Maria Eugenia |
author_sort | Gorgojo, Juan Pablo |
collection | PubMed |
description | B. parapertussis is one of the etiological agents of whooping cough. Once inhaled, the bacteria bind to the respiratory epithelium and start the infection. Little is known about this first step of host colonization and the role of the human airway epithelial barrier on B. parapertussis infection. We here investigated the outcome of the interaction of B. parapertussis with a polarized monolayer of respiratory epithelial cells. Our results show that B. parapertussis preferentially attaches to the intercellular boundaries, and causes the disruption of the tight junction integrity through the action of adenylate cyclase toxin (CyaA). We further found evidence indicating that this disruption enables the bacterial access to components of the basolateral membrane of epithelial cells to which B. parapertussis efficiently attaches and gains access to the intracellular location, where it can survive and eventually spread back into the extracellular environment. Altogether, these results suggest that the adenylate cyclase toxin enables B. parapertussis to overcome the epithelial barrier and eventually establish a niche of persistence within the respiratory epithelial cells. |
format | Online Article Text |
id | pubmed-10681170 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-106811702023-11-27 Adenylate cyclase toxin of Bordetella parapertussis disrupts the epithelial barrier granting the bacterial access to the intracellular space of epithelial cells Gorgojo, Juan Pablo Carrica, Mariela del Carmen Baroli, Carlos Manuel Valdez, Hugo Alberto Alvarez Hayes, Jimena Rodriguez, Maria Eugenia PLoS One Research Article B. parapertussis is one of the etiological agents of whooping cough. Once inhaled, the bacteria bind to the respiratory epithelium and start the infection. Little is known about this first step of host colonization and the role of the human airway epithelial barrier on B. parapertussis infection. We here investigated the outcome of the interaction of B. parapertussis with a polarized monolayer of respiratory epithelial cells. Our results show that B. parapertussis preferentially attaches to the intercellular boundaries, and causes the disruption of the tight junction integrity through the action of adenylate cyclase toxin (CyaA). We further found evidence indicating that this disruption enables the bacterial access to components of the basolateral membrane of epithelial cells to which B. parapertussis efficiently attaches and gains access to the intracellular location, where it can survive and eventually spread back into the extracellular environment. Altogether, these results suggest that the adenylate cyclase toxin enables B. parapertussis to overcome the epithelial barrier and eventually establish a niche of persistence within the respiratory epithelial cells. Public Library of Science 2023-11-27 /pmc/articles/PMC10681170/ /pubmed/38011105 http://dx.doi.org/10.1371/journal.pone.0291331 Text en © 2023 Gorgojo et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Gorgojo, Juan Pablo Carrica, Mariela del Carmen Baroli, Carlos Manuel Valdez, Hugo Alberto Alvarez Hayes, Jimena Rodriguez, Maria Eugenia Adenylate cyclase toxin of Bordetella parapertussis disrupts the epithelial barrier granting the bacterial access to the intracellular space of epithelial cells |
title | Adenylate cyclase toxin of Bordetella parapertussis disrupts the epithelial barrier granting the bacterial access to the intracellular space of epithelial cells |
title_full | Adenylate cyclase toxin of Bordetella parapertussis disrupts the epithelial barrier granting the bacterial access to the intracellular space of epithelial cells |
title_fullStr | Adenylate cyclase toxin of Bordetella parapertussis disrupts the epithelial barrier granting the bacterial access to the intracellular space of epithelial cells |
title_full_unstemmed | Adenylate cyclase toxin of Bordetella parapertussis disrupts the epithelial barrier granting the bacterial access to the intracellular space of epithelial cells |
title_short | Adenylate cyclase toxin of Bordetella parapertussis disrupts the epithelial barrier granting the bacterial access to the intracellular space of epithelial cells |
title_sort | adenylate cyclase toxin of bordetella parapertussis disrupts the epithelial barrier granting the bacterial access to the intracellular space of epithelial cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10681170/ https://www.ncbi.nlm.nih.gov/pubmed/38011105 http://dx.doi.org/10.1371/journal.pone.0291331 |
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