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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Biochemistry and Molecular Biology
2014
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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. |
format | Online Article Text |
id | pubmed-4067218 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
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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