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Cytoplasmic contractile injection systems mediate cell death in Streptomyces
Contractile injection systems (CIS) are bacteriophage tail-like structures that mediate bacterial cell–cell interactions. While CIS are highly abundant across diverse bacterial phyla, representative gene clusters in Gram-positive organisms remain poorly studied. Here we characterize a CIS in the Gra...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10066040/ https://www.ncbi.nlm.nih.gov/pubmed/36894633 http://dx.doi.org/10.1038/s41564-023-01341-x |
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author | Casu, Bastien Sallmen, Joseph W. Schlimpert, Susan Pilhofer, Martin |
author_facet | Casu, Bastien Sallmen, Joseph W. Schlimpert, Susan Pilhofer, Martin |
author_sort | Casu, Bastien |
collection | PubMed |
description | Contractile injection systems (CIS) are bacteriophage tail-like structures that mediate bacterial cell–cell interactions. While CIS are highly abundant across diverse bacterial phyla, representative gene clusters in Gram-positive organisms remain poorly studied. Here we characterize a CIS in the Gram-positive multicellular model organism Streptomyces coelicolor and show that, in contrast to most other CIS, S. coelicolor CIS (CIS(Sc)) mediate cell death in response to stress and impact cellular development. CIS(Sc) are expressed in the cytoplasm of vegetative hyphae and are not released into the medium. Our cryo-electron microscopy structure enabled the engineering of non-contractile and fluorescently tagged CIS(Sc) assemblies. Cryo-electron tomography showed that CIS(Sc) contraction is linked to reduced cellular integrity. Fluorescence light microscopy furthermore revealed that functional CIS(Sc) mediate cell death upon encountering different types of stress. The absence of functional CIS(Sc) had an impact on hyphal differentiation and secondary metabolite production. Finally, we identified three putative effector proteins, which when absent, phenocopied other CIS(Sc) mutants. Our results provide new functional insights into CIS in Gram-positive organisms and a framework for studying novel intracellular roles, including regulated cell death and life-cycle progression in multicellular bacteria. |
format | Online Article Text |
id | pubmed-10066040 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100660402023-04-02 Cytoplasmic contractile injection systems mediate cell death in Streptomyces Casu, Bastien Sallmen, Joseph W. Schlimpert, Susan Pilhofer, Martin Nat Microbiol Article Contractile injection systems (CIS) are bacteriophage tail-like structures that mediate bacterial cell–cell interactions. While CIS are highly abundant across diverse bacterial phyla, representative gene clusters in Gram-positive organisms remain poorly studied. Here we characterize a CIS in the Gram-positive multicellular model organism Streptomyces coelicolor and show that, in contrast to most other CIS, S. coelicolor CIS (CIS(Sc)) mediate cell death in response to stress and impact cellular development. CIS(Sc) are expressed in the cytoplasm of vegetative hyphae and are not released into the medium. Our cryo-electron microscopy structure enabled the engineering of non-contractile and fluorescently tagged CIS(Sc) assemblies. Cryo-electron tomography showed that CIS(Sc) contraction is linked to reduced cellular integrity. Fluorescence light microscopy furthermore revealed that functional CIS(Sc) mediate cell death upon encountering different types of stress. The absence of functional CIS(Sc) had an impact on hyphal differentiation and secondary metabolite production. Finally, we identified three putative effector proteins, which when absent, phenocopied other CIS(Sc) mutants. Our results provide new functional insights into CIS in Gram-positive organisms and a framework for studying novel intracellular roles, including regulated cell death and life-cycle progression in multicellular bacteria. Nature Publishing Group UK 2023-03-09 2023 /pmc/articles/PMC10066040/ /pubmed/36894633 http://dx.doi.org/10.1038/s41564-023-01341-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Casu, Bastien Sallmen, Joseph W. Schlimpert, Susan Pilhofer, Martin Cytoplasmic contractile injection systems mediate cell death in Streptomyces |
title | Cytoplasmic contractile injection systems mediate cell death in Streptomyces |
title_full | Cytoplasmic contractile injection systems mediate cell death in Streptomyces |
title_fullStr | Cytoplasmic contractile injection systems mediate cell death in Streptomyces |
title_full_unstemmed | Cytoplasmic contractile injection systems mediate cell death in Streptomyces |
title_short | Cytoplasmic contractile injection systems mediate cell death in Streptomyces |
title_sort | cytoplasmic contractile injection systems mediate cell death in streptomyces |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10066040/ https://www.ncbi.nlm.nih.gov/pubmed/36894633 http://dx.doi.org/10.1038/s41564-023-01341-x |
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