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Vibrio pore-forming leukocidin activates pyroptotic cell death via the NLRP3 inflammasome
Cell death mechanisms are central to combat infections and to drive inflammation. The inflammasome controls infection through activation of caspase-1 leading to either IL-1β dependent inflammation, or pyroptotic cell death in infected cells. Hemolysins, which are pore-forming toxins (PFTs), alter th...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7034064/ https://www.ncbi.nlm.nih.gov/pubmed/32013758 http://dx.doi.org/10.1080/22221751.2020.1720526 |
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author | Cohen, Hadar Baram, Noam Edry-Botzer, Liat Munitz, Ariel Salomon, Dor Gerlic, Motti |
author_facet | Cohen, Hadar Baram, Noam Edry-Botzer, Liat Munitz, Ariel Salomon, Dor Gerlic, Motti |
author_sort | Cohen, Hadar |
collection | PubMed |
description | Cell death mechanisms are central to combat infections and to drive inflammation. The inflammasome controls infection through activation of caspase-1 leading to either IL-1β dependent inflammation, or pyroptotic cell death in infected cells. Hemolysins, which are pore-forming toxins (PFTs), alter the permeability of the host target membrane, often leading to cell death. We previously discovered a leukocidin domain-containing PFT produced by the Gram-negative bacterium Vibrio proteolyticus, named VPRH. VPRH constitutes a distinct, understudied class within the leukocidin superfamily, which is distributed among several photogenic Vibrios. Since PFTs of other pathogens were shown to activate the inflammasome pathway, we hypothesized that VPRH-induced cell death is mediated by direct activation of the inflammasome in mammalian immune host cells. Indeed, we found that VPRH induced a two-step cell death in macrophages. The first, a rapid step, was mediated by activating the NLRP3 inflammasome, leading to caspase-1 activation that resulted in IL-1β secretion and pyroptosis. The second step was independent of the inflammasome; however, its mechanism remains unknown. This study sets the foundation for better understanding the immunological consequences of inflammasome activation by a new leukocidin class of toxins, which may be shared between marine bacteria and give rise to new pathogenic isolates. |
format | Online Article Text |
id | pubmed-7034064 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-70340642020-03-03 Vibrio pore-forming leukocidin activates pyroptotic cell death via the NLRP3 inflammasome Cohen, Hadar Baram, Noam Edry-Botzer, Liat Munitz, Ariel Salomon, Dor Gerlic, Motti Emerg Microbes Infect Article Cell death mechanisms are central to combat infections and to drive inflammation. The inflammasome controls infection through activation of caspase-1 leading to either IL-1β dependent inflammation, or pyroptotic cell death in infected cells. Hemolysins, which are pore-forming toxins (PFTs), alter the permeability of the host target membrane, often leading to cell death. We previously discovered a leukocidin domain-containing PFT produced by the Gram-negative bacterium Vibrio proteolyticus, named VPRH. VPRH constitutes a distinct, understudied class within the leukocidin superfamily, which is distributed among several photogenic Vibrios. Since PFTs of other pathogens were shown to activate the inflammasome pathway, we hypothesized that VPRH-induced cell death is mediated by direct activation of the inflammasome in mammalian immune host cells. Indeed, we found that VPRH induced a two-step cell death in macrophages. The first, a rapid step, was mediated by activating the NLRP3 inflammasome, leading to caspase-1 activation that resulted in IL-1β secretion and pyroptosis. The second step was independent of the inflammasome; however, its mechanism remains unknown. This study sets the foundation for better understanding the immunological consequences of inflammasome activation by a new leukocidin class of toxins, which may be shared between marine bacteria and give rise to new pathogenic isolates. Taylor & Francis 2020-02-04 /pmc/articles/PMC7034064/ /pubmed/32013758 http://dx.doi.org/10.1080/22221751.2020.1720526 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group, on behalf of Shanghai Shangyixun Cultural Communication Co., Ltd 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 | Article Cohen, Hadar Baram, Noam Edry-Botzer, Liat Munitz, Ariel Salomon, Dor Gerlic, Motti Vibrio pore-forming leukocidin activates pyroptotic cell death via the NLRP3 inflammasome |
title | Vibrio pore-forming leukocidin activates pyroptotic cell death via the NLRP3 inflammasome |
title_full | Vibrio pore-forming leukocidin activates pyroptotic cell death via the NLRP3 inflammasome |
title_fullStr | Vibrio pore-forming leukocidin activates pyroptotic cell death via the NLRP3 inflammasome |
title_full_unstemmed | Vibrio pore-forming leukocidin activates pyroptotic cell death via the NLRP3 inflammasome |
title_short | Vibrio pore-forming leukocidin activates pyroptotic cell death via the NLRP3 inflammasome |
title_sort | vibrio pore-forming leukocidin activates pyroptotic cell death via the nlrp3 inflammasome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7034064/ https://www.ncbi.nlm.nih.gov/pubmed/32013758 http://dx.doi.org/10.1080/22221751.2020.1720526 |
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