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Clostridium perfringens α-Toxin Impairs Innate Immunity via Inhibition of Neutrophil Differentiation
Although granulopoiesis is accelerated to suppress bacteria during infection, some bacteria can still cause life-threatening infections, but the mechanism behind this remains unclear. In this study, we found that mature neutrophils in bone marrow cells (BMCs) were decreased in C. perfringens-infecte...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4910053/ https://www.ncbi.nlm.nih.gov/pubmed/27306065 http://dx.doi.org/10.1038/srep28192 |
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author | Takehara, Masaya Takagishi, Teruhisa Seike, Soshi Ohtani, Kaori Kobayashi, Keiko Miyamoto, Kazuaki Shimizu, Tohru Nagahama, Masahiro |
author_facet | Takehara, Masaya Takagishi, Teruhisa Seike, Soshi Ohtani, Kaori Kobayashi, Keiko Miyamoto, Kazuaki Shimizu, Tohru Nagahama, Masahiro |
author_sort | Takehara, Masaya |
collection | PubMed |
description | Although granulopoiesis is accelerated to suppress bacteria during infection, some bacteria can still cause life-threatening infections, but the mechanism behind this remains unclear. In this study, we found that mature neutrophils in bone marrow cells (BMCs) were decreased in C. perfringens-infected mice and also after injection of virulence factor α-toxin. C. perfringens infection interfered with the replenishment of mature neutrophils in the peripheral circulation and the accumulation of neutrophils at C. perfringens-infected sites in an α-toxin-dependent manner. Measurements of bacterial colony-forming units in C. perfringens-infected muscle revealed that α-toxin inhibited a reduction in the load of C. perfringens. In vitro treatment of isolated BMCs with α-toxin (phospholipase C) revealed that α-toxin directly decreased mature neutrophils. α-Toxin did not influence the viability of isolated mature neutrophils, while simultaneous treatment of BMCs with granulocyte colony-stimulating factor attenuated the reduction of mature neutrophils by α-toxin. Together, our results illustrate that impairment of the innate immune system by the inhibition of neutrophil differentiation is crucial for the pathogenesis of C. perfringens to promote disease to a life-threatening infection, which provides new insight to understand how pathogenic bacteria evade the host immune system. |
format | Online Article Text |
id | pubmed-4910053 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49100532016-06-16 Clostridium perfringens α-Toxin Impairs Innate Immunity via Inhibition of Neutrophil Differentiation Takehara, Masaya Takagishi, Teruhisa Seike, Soshi Ohtani, Kaori Kobayashi, Keiko Miyamoto, Kazuaki Shimizu, Tohru Nagahama, Masahiro Sci Rep Article Although granulopoiesis is accelerated to suppress bacteria during infection, some bacteria can still cause life-threatening infections, but the mechanism behind this remains unclear. In this study, we found that mature neutrophils in bone marrow cells (BMCs) were decreased in C. perfringens-infected mice and also after injection of virulence factor α-toxin. C. perfringens infection interfered with the replenishment of mature neutrophils in the peripheral circulation and the accumulation of neutrophils at C. perfringens-infected sites in an α-toxin-dependent manner. Measurements of bacterial colony-forming units in C. perfringens-infected muscle revealed that α-toxin inhibited a reduction in the load of C. perfringens. In vitro treatment of isolated BMCs with α-toxin (phospholipase C) revealed that α-toxin directly decreased mature neutrophils. α-Toxin did not influence the viability of isolated mature neutrophils, while simultaneous treatment of BMCs with granulocyte colony-stimulating factor attenuated the reduction of mature neutrophils by α-toxin. Together, our results illustrate that impairment of the innate immune system by the inhibition of neutrophil differentiation is crucial for the pathogenesis of C. perfringens to promote disease to a life-threatening infection, which provides new insight to understand how pathogenic bacteria evade the host immune system. Nature Publishing Group 2016-06-16 /pmc/articles/PMC4910053/ /pubmed/27306065 http://dx.doi.org/10.1038/srep28192 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Takehara, Masaya Takagishi, Teruhisa Seike, Soshi Ohtani, Kaori Kobayashi, Keiko Miyamoto, Kazuaki Shimizu, Tohru Nagahama, Masahiro Clostridium perfringens α-Toxin Impairs Innate Immunity via Inhibition of Neutrophil Differentiation |
title | Clostridium perfringens α-Toxin Impairs Innate Immunity via Inhibition of Neutrophil Differentiation |
title_full | Clostridium perfringens α-Toxin Impairs Innate Immunity via Inhibition of Neutrophil Differentiation |
title_fullStr | Clostridium perfringens α-Toxin Impairs Innate Immunity via Inhibition of Neutrophil Differentiation |
title_full_unstemmed | Clostridium perfringens α-Toxin Impairs Innate Immunity via Inhibition of Neutrophil Differentiation |
title_short | Clostridium perfringens α-Toxin Impairs Innate Immunity via Inhibition of Neutrophil Differentiation |
title_sort | clostridium perfringens α-toxin impairs innate immunity via inhibition of neutrophil differentiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4910053/ https://www.ncbi.nlm.nih.gov/pubmed/27306065 http://dx.doi.org/10.1038/srep28192 |
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