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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...

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Autores principales: Jiang, Nan, Tang, Le, Xie, Ruiqiang, Li, Zhi, Burkinshaw, Brianne, Liang, Xiaoye, Sosa, Dylan, Aravind, L., Dong, Tao, Zhang, Dapeng, Zheng, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
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.
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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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