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Vibrio parahaemolyticus RhsP represents a widespread group of pro-effectors for type VI secretion systems
Type VI secretion systems (T6SSs) translocate effector proteins, such as Rhs toxins, to eukaryotic cells or prokaryotic competitors. All T6SS Rhs-type effectors characterized thus far contain a PAAR motif or a similar structure. Here, we describe a T6SS-dependent delivery mechanism for a subset of R...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156420/ https://www.ncbi.nlm.nih.gov/pubmed/30254227 http://dx.doi.org/10.1038/s41467-018-06201-5 |
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author | Jiang, Nan Tang, Le Xie, Ruiqiang Li, Zhi Burkinshaw, Brianne Liang, Xiaoye Sosa, Dylan Aravind, L. Dong, Tao Zhang, Dapeng Zheng, Jun |
author_facet | Jiang, Nan Tang, Le Xie, Ruiqiang Li, Zhi Burkinshaw, Brianne Liang, Xiaoye Sosa, Dylan Aravind, L. Dong, Tao Zhang, Dapeng Zheng, Jun |
author_sort | Jiang, Nan |
collection | PubMed |
description | Type VI secretion systems (T6SSs) translocate effector proteins, such as Rhs toxins, to eukaryotic cells or prokaryotic competitors. All T6SS Rhs-type effectors characterized thus far contain a PAAR motif or a similar structure. Here, we describe a T6SS-dependent delivery mechanism for a subset of Rhs proteins that lack a PAAR motif. We show that the N-terminal Rhs domain of protein RhsP (or VP1517) from Vibrio parahaemolyticus inhibits the activity of the C-terminal DNase domain. Upon auto-proteolysis, the Rhs fragment remains inside the cells, and the C-terminal region interacts with PAAR2 and is secreted by T6SS2; therefore, RhsP acts as a pro-effector. Furthermore, we show that RhsP contributes to the control of certain “social cheaters” (opaR mutants). Genes encoding proteins with similar Rhs and PAAR-interacting domains, but diverse C-terminal regions, are widely distributed among Vibrio species. |
format | Online Article Text |
id | pubmed-6156420 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61564202018-09-27 Vibrio parahaemolyticus RhsP represents a widespread group of pro-effectors for type VI secretion systems Jiang, Nan Tang, Le Xie, Ruiqiang Li, Zhi Burkinshaw, Brianne Liang, Xiaoye Sosa, Dylan Aravind, L. Dong, Tao Zhang, Dapeng Zheng, Jun Nat Commun Article Type VI secretion systems (T6SSs) translocate effector proteins, such as Rhs toxins, to eukaryotic cells or prokaryotic competitors. All T6SS Rhs-type effectors characterized thus far contain a PAAR motif or a similar structure. Here, we describe a T6SS-dependent delivery mechanism for a subset of Rhs proteins that lack a PAAR motif. We show that the N-terminal Rhs domain of protein RhsP (or VP1517) from Vibrio parahaemolyticus inhibits the activity of the C-terminal DNase domain. Upon auto-proteolysis, the Rhs fragment remains inside the cells, and the C-terminal region interacts with PAAR2 and is secreted by T6SS2; therefore, RhsP acts as a pro-effector. Furthermore, we show that RhsP contributes to the control of certain “social cheaters” (opaR mutants). Genes encoding proteins with similar Rhs and PAAR-interacting domains, but diverse C-terminal regions, are widely distributed among Vibrio species. Nature Publishing Group UK 2018-09-25 /pmc/articles/PMC6156420/ /pubmed/30254227 http://dx.doi.org/10.1038/s41467-018-06201-5 Text en © The Author(s) 2018 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/. |
spellingShingle | Article Jiang, Nan Tang, Le Xie, Ruiqiang Li, Zhi Burkinshaw, Brianne Liang, Xiaoye Sosa, Dylan Aravind, L. Dong, Tao Zhang, Dapeng Zheng, Jun Vibrio parahaemolyticus RhsP represents a widespread group of pro-effectors for type VI secretion systems |
title | Vibrio parahaemolyticus RhsP represents a widespread group of pro-effectors for type VI secretion systems |
title_full | Vibrio parahaemolyticus RhsP represents a widespread group of pro-effectors for type VI secretion systems |
title_fullStr | Vibrio parahaemolyticus RhsP represents a widespread group of pro-effectors for type VI secretion systems |
title_full_unstemmed | Vibrio parahaemolyticus RhsP represents a widespread group of pro-effectors for type VI secretion systems |
title_short | Vibrio parahaemolyticus RhsP represents a widespread group of pro-effectors for type VI secretion systems |
title_sort | vibrio parahaemolyticus rhsp represents a widespread group of pro-effectors for type vi secretion systems |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156420/ https://www.ncbi.nlm.nih.gov/pubmed/30254227 http://dx.doi.org/10.1038/s41467-018-06201-5 |
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