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Identification and structure of an extracellular contractile injection system from the marine bacterium Algoriphagus machipongonensis

Contractile injection systems (CISs) are phage tail-like nanomachines, mediating bacterial cell–cell interactions as either type VI secretion systems (T6SSs) or extracellular CISs (eCISs). Bioinformatic studies uncovered a phylogenetic group of hundreds of putative CIS gene clusters that are highly...

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Autores principales: Xu, Jingwei, Ericson, Charles F., Lien, Yun-Wei, Rutaganira, Florentine U. N., Eisenstein, Fabian, Feldmüller, Miki, King, Nicole, Pilhofer, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8894135/
https://www.ncbi.nlm.nih.gov/pubmed/35165385
http://dx.doi.org/10.1038/s41564-022-01059-2
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author Xu, Jingwei
Ericson, Charles F.
Lien, Yun-Wei
Rutaganira, Florentine U. N.
Eisenstein, Fabian
Feldmüller, Miki
King, Nicole
Pilhofer, Martin
author_facet Xu, Jingwei
Ericson, Charles F.
Lien, Yun-Wei
Rutaganira, Florentine U. N.
Eisenstein, Fabian
Feldmüller, Miki
King, Nicole
Pilhofer, Martin
author_sort Xu, Jingwei
collection PubMed
description Contractile injection systems (CISs) are phage tail-like nanomachines, mediating bacterial cell–cell interactions as either type VI secretion systems (T6SSs) or extracellular CISs (eCISs). Bioinformatic studies uncovered a phylogenetic group of hundreds of putative CIS gene clusters that are highly diverse and widespread; however, only four systems have been characterized. Here we studied a putative CIS gene cluster in the marine bacterium Algoriphagus machipongonensis. Using an integrative approach, we show that the system is compatible with an eCIS mode of action. Our cryo-electron microscopy structure revealed several features that differ from those seen in other CISs: a ‘cap adaptor’ located at the distal end, a ‘plug’ exposed to the tube lumen, and a ‘cage’ formed by massive extensions of the baseplate. These elements are conserved in other CISs, and our genetic tools identified that they are required for assembly, cargo loading and function. Furthermore, our atomic model highlights specific evolutionary hotspots and will serve as a framework for understanding and re−engineering CISs.
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spelling pubmed-88941352022-03-22 Identification and structure of an extracellular contractile injection system from the marine bacterium Algoriphagus machipongonensis Xu, Jingwei Ericson, Charles F. Lien, Yun-Wei Rutaganira, Florentine U. N. Eisenstein, Fabian Feldmüller, Miki King, Nicole Pilhofer, Martin Nat Microbiol Article Contractile injection systems (CISs) are phage tail-like nanomachines, mediating bacterial cell–cell interactions as either type VI secretion systems (T6SSs) or extracellular CISs (eCISs). Bioinformatic studies uncovered a phylogenetic group of hundreds of putative CIS gene clusters that are highly diverse and widespread; however, only four systems have been characterized. Here we studied a putative CIS gene cluster in the marine bacterium Algoriphagus machipongonensis. Using an integrative approach, we show that the system is compatible with an eCIS mode of action. Our cryo-electron microscopy structure revealed several features that differ from those seen in other CISs: a ‘cap adaptor’ located at the distal end, a ‘plug’ exposed to the tube lumen, and a ‘cage’ formed by massive extensions of the baseplate. These elements are conserved in other CISs, and our genetic tools identified that they are required for assembly, cargo loading and function. Furthermore, our atomic model highlights specific evolutionary hotspots and will serve as a framework for understanding and re−engineering CISs. Nature Publishing Group UK 2022-02-14 2022 /pmc/articles/PMC8894135/ /pubmed/35165385 http://dx.doi.org/10.1038/s41564-022-01059-2 Text en © The Author(s) 2022, corrected publication 2022 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
Xu, Jingwei
Ericson, Charles F.
Lien, Yun-Wei
Rutaganira, Florentine U. N.
Eisenstein, Fabian
Feldmüller, Miki
King, Nicole
Pilhofer, Martin
Identification and structure of an extracellular contractile injection system from the marine bacterium Algoriphagus machipongonensis
title Identification and structure of an extracellular contractile injection system from the marine bacterium Algoriphagus machipongonensis
title_full Identification and structure of an extracellular contractile injection system from the marine bacterium Algoriphagus machipongonensis
title_fullStr Identification and structure of an extracellular contractile injection system from the marine bacterium Algoriphagus machipongonensis
title_full_unstemmed Identification and structure of an extracellular contractile injection system from the marine bacterium Algoriphagus machipongonensis
title_short Identification and structure of an extracellular contractile injection system from the marine bacterium Algoriphagus machipongonensis
title_sort identification and structure of an extracellular contractile injection system from the marine bacterium algoriphagus machipongonensis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8894135/
https://www.ncbi.nlm.nih.gov/pubmed/35165385
http://dx.doi.org/10.1038/s41564-022-01059-2
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