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The Achromobacter type 3 secretion system drives pyroptosis and immunopathology via independent activation of NLRC4 and NLRP3 inflammasomes
How the opportunistic Gram-negative pathogens of the genus Achromobacter interact with the innate immune system is poorly understood. Using three Achromobacter clinical isolates from two species, we show that the type 3 secretion system (T3SS) is required to induce cell death in human macrophages by...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7614980/ https://www.ncbi.nlm.nih.gov/pubmed/37598340 http://dx.doi.org/10.1016/j.celrep.2023.113012 |
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author | Turton, Keren Parks, Hannah J. Zarodkiewicz, Paulina Hamad, Mohamad A. Dwane, Rachel Parau, Georgiana Ingram, Rebecca J. Coll, Rebecca C. Bryant, Clare E. Valvano, Miguel A. |
author_facet | Turton, Keren Parks, Hannah J. Zarodkiewicz, Paulina Hamad, Mohamad A. Dwane, Rachel Parau, Georgiana Ingram, Rebecca J. Coll, Rebecca C. Bryant, Clare E. Valvano, Miguel A. |
author_sort | Turton, Keren |
collection | PubMed |
description | How the opportunistic Gram-negative pathogens of the genus Achromobacter interact with the innate immune system is poorly understood. Using three Achromobacter clinical isolates from two species, we show that the type 3 secretion system (T3SS) is required to induce cell death in human macrophages by inflammasome-dependent pyroptosis. Macrophages deficient in the inflammasome sensors NLRC4 or NLRP3 undergo pyroptosis upon bacterial internalization, but those deficient in both NLRC4 and NLRP3 do not, suggesting either sensor mediates pyroptosis in a T3SS-dependent manner. Detailed analysis of the intracellular trafficking of one isolate indicates that the intracellular bacteria reside in a late phagolysosome. Using an intranasal mouse infection model, we observe that Achromobacter damages lung structure and causes severe illness, contingent on a functional T3SS. Together, we demonstrate that Achromobacter species can survive phagocytosis by promoting macrophage cell death and inflammation by redundant mechanisms of pyroptosis induction in a T3SS-dependent manner. |
format | Online Article Text |
id | pubmed-7614980 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
record_format | MEDLINE/PubMed |
spelling | pubmed-76149802023-08-25 The Achromobacter type 3 secretion system drives pyroptosis and immunopathology via independent activation of NLRC4 and NLRP3 inflammasomes Turton, Keren Parks, Hannah J. Zarodkiewicz, Paulina Hamad, Mohamad A. Dwane, Rachel Parau, Georgiana Ingram, Rebecca J. Coll, Rebecca C. Bryant, Clare E. Valvano, Miguel A. Cell Rep Article How the opportunistic Gram-negative pathogens of the genus Achromobacter interact with the innate immune system is poorly understood. Using three Achromobacter clinical isolates from two species, we show that the type 3 secretion system (T3SS) is required to induce cell death in human macrophages by inflammasome-dependent pyroptosis. Macrophages deficient in the inflammasome sensors NLRC4 or NLRP3 undergo pyroptosis upon bacterial internalization, but those deficient in both NLRC4 and NLRP3 do not, suggesting either sensor mediates pyroptosis in a T3SS-dependent manner. Detailed analysis of the intracellular trafficking of one isolate indicates that the intracellular bacteria reside in a late phagolysosome. Using an intranasal mouse infection model, we observe that Achromobacter damages lung structure and causes severe illness, contingent on a functional T3SS. Together, we demonstrate that Achromobacter species can survive phagocytosis by promoting macrophage cell death and inflammation by redundant mechanisms of pyroptosis induction in a T3SS-dependent manner. 2023-08-19 2023-08-19 /pmc/articles/PMC7614980/ /pubmed/37598340 http://dx.doi.org/10.1016/j.celrep.2023.113012 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a BY 4.0 (https://creativecommons.org/licenses/by/4.0/) International license. |
spellingShingle | Article Turton, Keren Parks, Hannah J. Zarodkiewicz, Paulina Hamad, Mohamad A. Dwane, Rachel Parau, Georgiana Ingram, Rebecca J. Coll, Rebecca C. Bryant, Clare E. Valvano, Miguel A. The Achromobacter type 3 secretion system drives pyroptosis and immunopathology via independent activation of NLRC4 and NLRP3 inflammasomes |
title | The Achromobacter type 3 secretion system drives pyroptosis and immunopathology via independent activation of NLRC4 and NLRP3 inflammasomes |
title_full | The Achromobacter type 3 secretion system drives pyroptosis and immunopathology via independent activation of NLRC4 and NLRP3 inflammasomes |
title_fullStr | The Achromobacter type 3 secretion system drives pyroptosis and immunopathology via independent activation of NLRC4 and NLRP3 inflammasomes |
title_full_unstemmed | The Achromobacter type 3 secretion system drives pyroptosis and immunopathology via independent activation of NLRC4 and NLRP3 inflammasomes |
title_short | The Achromobacter type 3 secretion system drives pyroptosis and immunopathology via independent activation of NLRC4 and NLRP3 inflammasomes |
title_sort | achromobacter type 3 secretion system drives pyroptosis and immunopathology via independent activation of nlrc4 and nlrp3 inflammasomes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7614980/ https://www.ncbi.nlm.nih.gov/pubmed/37598340 http://dx.doi.org/10.1016/j.celrep.2023.113012 |
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