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The VgrG Proteins Are “à la Carte” Delivery Systems for Bacterial Type VI Effectors

The bacterial type VI secretion system (T6SS) is a supra-molecular complex akin to bacteriophage tails, with VgrG proteins acting as a puncturing device. The Pseudomonas aeruginosa H1-T6SS has been extensively characterized. It is involved in bacterial killing and in the delivery of three toxins, Ts...

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Autores principales: Hachani, Abderrahman, Allsopp, Luke P., Oduko, Yewande, Filloux, Alain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4067218/
https://www.ncbi.nlm.nih.gov/pubmed/24794869
http://dx.doi.org/10.1074/jbc.M114.563429
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author Hachani, Abderrahman
Allsopp, Luke P.
Oduko, Yewande
Filloux, Alain
author_facet Hachani, Abderrahman
Allsopp, Luke P.
Oduko, Yewande
Filloux, Alain
author_sort Hachani, Abderrahman
collection PubMed
description The bacterial type VI secretion system (T6SS) is a supra-molecular complex akin to bacteriophage tails, with VgrG proteins acting as a puncturing device. The Pseudomonas aeruginosa H1-T6SS has been extensively characterized. It is involved in bacterial killing and in the delivery of three toxins, Tse1–3. Here, we demonstrate the independent contribution of the three H1-T6SS co-regulated vgrG genes, vgrG1abc, to bacterial killing. A putative toxin is encoded in the vicinity of each vgrG gene, supporting the concept of specific VgrG/toxin couples. In this respect, VgrG1c is involved in the delivery of an Rhs protein, RhsP1. The RhsP1 C terminus carries a toxic activity, from which the producing bacterium is protected by a cognate immunity. Similarly, VgrG1a-dependent toxicity is associated with the PA0093 gene encoding a two-domain protein with a putative toxin domain (Toxin_61) at the C terminus. Finally, VgrG1b-dependent killing is detectable upon complementation of a triple vgrG1abc mutant. The VgrG1b-dependent killing is mediated by PA0099, which presents the characteristics of the superfamily nuclease 2 toxin members. Overall, these data develop the concept that VgrGs are indispensable components for the specific delivery of effectors. Several additional vgrG genes are encoded on the P. aeruginosa genome and are not linked genetically to other T6SS genes. A closer inspection of these clusters reveals that they also encode putative toxins. Overall, these associations further support the notion of an original form of secretion system, in which VgrG acts as the carrier.
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spelling pubmed-40672182014-06-25 The VgrG Proteins Are “à la Carte” Delivery Systems for Bacterial Type VI Effectors Hachani, Abderrahman Allsopp, Luke P. Oduko, Yewande Filloux, Alain J Biol Chem Microbiology The bacterial type VI secretion system (T6SS) is a supra-molecular complex akin to bacteriophage tails, with VgrG proteins acting as a puncturing device. The Pseudomonas aeruginosa H1-T6SS has been extensively characterized. It is involved in bacterial killing and in the delivery of three toxins, Tse1–3. Here, we demonstrate the independent contribution of the three H1-T6SS co-regulated vgrG genes, vgrG1abc, to bacterial killing. A putative toxin is encoded in the vicinity of each vgrG gene, supporting the concept of specific VgrG/toxin couples. In this respect, VgrG1c is involved in the delivery of an Rhs protein, RhsP1. The RhsP1 C terminus carries a toxic activity, from which the producing bacterium is protected by a cognate immunity. Similarly, VgrG1a-dependent toxicity is associated with the PA0093 gene encoding a two-domain protein with a putative toxin domain (Toxin_61) at the C terminus. Finally, VgrG1b-dependent killing is detectable upon complementation of a triple vgrG1abc mutant. The VgrG1b-dependent killing is mediated by PA0099, which presents the characteristics of the superfamily nuclease 2 toxin members. Overall, these data develop the concept that VgrGs are indispensable components for the specific delivery of effectors. Several additional vgrG genes are encoded on the P. aeruginosa genome and are not linked genetically to other T6SS genes. A closer inspection of these clusters reveals that they also encode putative toxins. Overall, these associations further support the notion of an original form of secretion system, in which VgrG acts as the carrier. American Society for Biochemistry and Molecular Biology 2014-06-20 2014-05-02 /pmc/articles/PMC4067218/ /pubmed/24794869 http://dx.doi.org/10.1074/jbc.M114.563429 Text en © 2014 by The American Society for Biochemistry and Molecular Biology, Inc. Author's Choice—Final version full access. Creative Commons Attribution Unported License (http://creativecommons.org/licenses/by/3.0/) applies to Author Choice Articles
spellingShingle Microbiology
Hachani, Abderrahman
Allsopp, Luke P.
Oduko, Yewande
Filloux, Alain
The VgrG Proteins Are “à la Carte” Delivery Systems for Bacterial Type VI Effectors
title The VgrG Proteins Are “à la Carte” Delivery Systems for Bacterial Type VI Effectors
title_full The VgrG Proteins Are “à la Carte” Delivery Systems for Bacterial Type VI Effectors
title_fullStr The VgrG Proteins Are “à la Carte” Delivery Systems for Bacterial Type VI Effectors
title_full_unstemmed The VgrG Proteins Are “à la Carte” Delivery Systems for Bacterial Type VI Effectors
title_short The VgrG Proteins Are “à la Carte” Delivery Systems for Bacterial Type VI Effectors
title_sort vgrg proteins are “à la carte” delivery systems for bacterial type vi effectors
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4067218/
https://www.ncbi.nlm.nih.gov/pubmed/24794869
http://dx.doi.org/10.1074/jbc.M114.563429
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