Pseudomonas aeruginosa Exolysin promotes bacterial growth in lungs, alveolar damage and bacterial dissemination
Abstract Exolysin (ExlA) is a recently-identified pore-forming toxin secreted by a subset of Pseudomonas aeruginosa strains identified worldwide and devoid of Type III secretion system (T3SS), a major virulence factor. Here, we characterized at the ultrastructural level the lesions caused by an ExlA...
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2017-05-01
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doaj-4f0fdf56379345839d8f59e1a599bd972020-12-08T02:50:14ZengNature Publishing GroupScientific Reports2045-23222017-05-017111110.1038/s41598-017-02349-0Pseudomonas aeruginosa Exolysin promotes bacterial growth in lungs, alveolar damage and bacterial disseminationStéphanie Bouillot0Patrick Munro1Benoit Gallet2Emeline Reboud3François Cretin4Guillaume Golovkine5Guy Schoehn6Ina Attrée7Emmanuel Lemichez8Philippe Huber9Université Grenoble AlpesINSERM, U1065Université Grenoble AlpesUniversité Grenoble AlpesUniversité Grenoble AlpesUniversité Grenoble AlpesUniversité Grenoble AlpesUniversité Grenoble AlpesINSERM, U1065Université Grenoble AlpesAbstract Exolysin (ExlA) is a recently-identified pore-forming toxin secreted by a subset of Pseudomonas aeruginosa strains identified worldwide and devoid of Type III secretion system (T3SS), a major virulence factor. Here, we characterized at the ultrastructural level the lesions caused by an ExlA-secreting strain, CLJ1, in mouse infected lungs. CLJ1 induced necrotic lesions in pneumocytes and endothelial cells, resulting in alveolo-vascular barrier breakdown. Ectopic expression of ExlA in an exlA-negative strain induced similar tissue injuries. In addition, ExlA conferred on bacteria the capacity to proliferate in lungs and to disseminate in secondary organs, similar to bacteria possessing a functional T3SS. CLJ1 did not promote a strong neutrophil infiltration in the alveoli, owing to the weak pro-inflammatory cytokine reaction engendered by the strain. However, CLJ1 was rapidly eliminated from the blood in a bacteremia model, suggesting that it can be promptly phagocytosed by immune cells. Together, our study ascribes to ExlA-secreting bacteria the capacity to proliferate in the lung and to damage pulmonary tissues, thereby promoting metastatic infections, in absence of substantial immune response exacerbation.https://doi.org/10.1038/s41598-017-02349-0 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Stéphanie Bouillot Patrick Munro Benoit Gallet Emeline Reboud François Cretin Guillaume Golovkine Guy Schoehn Ina Attrée Emmanuel Lemichez Philippe Huber |
spellingShingle |
Stéphanie Bouillot Patrick Munro Benoit Gallet Emeline Reboud François Cretin Guillaume Golovkine Guy Schoehn Ina Attrée Emmanuel Lemichez Philippe Huber Pseudomonas aeruginosa Exolysin promotes bacterial growth in lungs, alveolar damage and bacterial dissemination Scientific Reports |
author_facet |
Stéphanie Bouillot Patrick Munro Benoit Gallet Emeline Reboud François Cretin Guillaume Golovkine Guy Schoehn Ina Attrée Emmanuel Lemichez Philippe Huber |
author_sort |
Stéphanie Bouillot |
title |
Pseudomonas aeruginosa Exolysin promotes bacterial growth in lungs, alveolar damage and bacterial dissemination |
title_short |
Pseudomonas aeruginosa Exolysin promotes bacterial growth in lungs, alveolar damage and bacterial dissemination |
title_full |
Pseudomonas aeruginosa Exolysin promotes bacterial growth in lungs, alveolar damage and bacterial dissemination |
title_fullStr |
Pseudomonas aeruginosa Exolysin promotes bacterial growth in lungs, alveolar damage and bacterial dissemination |
title_full_unstemmed |
Pseudomonas aeruginosa Exolysin promotes bacterial growth in lungs, alveolar damage and bacterial dissemination |
title_sort |
pseudomonas aeruginosa exolysin promotes bacterial growth in lungs, alveolar damage and bacterial dissemination |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2017-05-01 |
description |
Abstract Exolysin (ExlA) is a recently-identified pore-forming toxin secreted by a subset of Pseudomonas aeruginosa strains identified worldwide and devoid of Type III secretion system (T3SS), a major virulence factor. Here, we characterized at the ultrastructural level the lesions caused by an ExlA-secreting strain, CLJ1, in mouse infected lungs. CLJ1 induced necrotic lesions in pneumocytes and endothelial cells, resulting in alveolo-vascular barrier breakdown. Ectopic expression of ExlA in an exlA-negative strain induced similar tissue injuries. In addition, ExlA conferred on bacteria the capacity to proliferate in lungs and to disseminate in secondary organs, similar to bacteria possessing a functional T3SS. CLJ1 did not promote a strong neutrophil infiltration in the alveoli, owing to the weak pro-inflammatory cytokine reaction engendered by the strain. However, CLJ1 was rapidly eliminated from the blood in a bacteremia model, suggesting that it can be promptly phagocytosed by immune cells. Together, our study ascribes to ExlA-secreting bacteria the capacity to proliferate in the lung and to damage pulmonary tissues, thereby promoting metastatic infections, in absence of substantial immune response exacerbation. |
url |
https://doi.org/10.1038/s41598-017-02349-0 |
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