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Actin activates Pseudomonas aeruginosa ExoY nucleotidyl cyclase toxin and ExoY-like effector domains from MARTX toxins
The nucleotidyl cyclase toxin ExoY is one of the virulence factors injected by the Pseudomonas aeruginosa type III secretion system into host cells. Inside cells, it is activated by an unknown eukaryotic cofactor to synthesize various cyclic nucleotide monophosphates. ExoY-like adenylate cyclases ar...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5150216/ https://www.ncbi.nlm.nih.gov/pubmed/27917880 http://dx.doi.org/10.1038/ncomms13582 |
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author | Belyy, Alexander Raoux-Barbot, Dorothée Saveanu, Cosmin Namane, Abdelkader Ogryzko, Vasily Worpenberg, Lina David, Violaine Henriot, Veronique Fellous, Souad Merrifield, Christien Assayag, Elodie Ladant, Daniel Renault, Louis Mechold, Undine |
author_facet | Belyy, Alexander Raoux-Barbot, Dorothée Saveanu, Cosmin Namane, Abdelkader Ogryzko, Vasily Worpenberg, Lina David, Violaine Henriot, Veronique Fellous, Souad Merrifield, Christien Assayag, Elodie Ladant, Daniel Renault, Louis Mechold, Undine |
author_sort | Belyy, Alexander |
collection | PubMed |
description | The nucleotidyl cyclase toxin ExoY is one of the virulence factors injected by the Pseudomonas aeruginosa type III secretion system into host cells. Inside cells, it is activated by an unknown eukaryotic cofactor to synthesize various cyclic nucleotide monophosphates. ExoY-like adenylate cyclases are also found in Multifunctional-Autoprocessing Repeats-in-ToXin (MARTX) toxins produced by various Gram-negative pathogens. Here we demonstrate that filamentous actin (F-actin) is the hitherto unknown cofactor of ExoY. Association with F-actin stimulates ExoY activity more than 10,000 fold in vitro and results in stabilization of actin filaments. ExoY is recruited to actin filaments in transfected cells and alters F-actin turnover. Actin also activates an ExoY-like adenylate cyclase MARTX effector domain from Vibrio nigripulchritudo. Finally, using a yeast genetic screen, we identify actin mutants that no longer activate ExoY. Our results thus reveal a new sub-group within the class II adenylyl cyclase family, namely actin-activated nucleotidyl cyclase (AA-NC) toxins. |
format | Online Article Text |
id | pubmed-5150216 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51502162016-12-21 Actin activates Pseudomonas aeruginosa ExoY nucleotidyl cyclase toxin and ExoY-like effector domains from MARTX toxins Belyy, Alexander Raoux-Barbot, Dorothée Saveanu, Cosmin Namane, Abdelkader Ogryzko, Vasily Worpenberg, Lina David, Violaine Henriot, Veronique Fellous, Souad Merrifield, Christien Assayag, Elodie Ladant, Daniel Renault, Louis Mechold, Undine Nat Commun Article The nucleotidyl cyclase toxin ExoY is one of the virulence factors injected by the Pseudomonas aeruginosa type III secretion system into host cells. Inside cells, it is activated by an unknown eukaryotic cofactor to synthesize various cyclic nucleotide monophosphates. ExoY-like adenylate cyclases are also found in Multifunctional-Autoprocessing Repeats-in-ToXin (MARTX) toxins produced by various Gram-negative pathogens. Here we demonstrate that filamentous actin (F-actin) is the hitherto unknown cofactor of ExoY. Association with F-actin stimulates ExoY activity more than 10,000 fold in vitro and results in stabilization of actin filaments. ExoY is recruited to actin filaments in transfected cells and alters F-actin turnover. Actin also activates an ExoY-like adenylate cyclase MARTX effector domain from Vibrio nigripulchritudo. Finally, using a yeast genetic screen, we identify actin mutants that no longer activate ExoY. Our results thus reveal a new sub-group within the class II adenylyl cyclase family, namely actin-activated nucleotidyl cyclase (AA-NC) toxins. Nature Publishing Group 2016-12-05 /pmc/articles/PMC5150216/ /pubmed/27917880 http://dx.doi.org/10.1038/ncomms13582 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Belyy, Alexander Raoux-Barbot, Dorothée Saveanu, Cosmin Namane, Abdelkader Ogryzko, Vasily Worpenberg, Lina David, Violaine Henriot, Veronique Fellous, Souad Merrifield, Christien Assayag, Elodie Ladant, Daniel Renault, Louis Mechold, Undine Actin activates Pseudomonas aeruginosa ExoY nucleotidyl cyclase toxin and ExoY-like effector domains from MARTX toxins |
title | Actin activates Pseudomonas aeruginosa ExoY nucleotidyl cyclase toxin and ExoY-like effector domains from MARTX toxins |
title_full | Actin activates Pseudomonas aeruginosa ExoY nucleotidyl cyclase toxin and ExoY-like effector domains from MARTX toxins |
title_fullStr | Actin activates Pseudomonas aeruginosa ExoY nucleotidyl cyclase toxin and ExoY-like effector domains from MARTX toxins |
title_full_unstemmed | Actin activates Pseudomonas aeruginosa ExoY nucleotidyl cyclase toxin and ExoY-like effector domains from MARTX toxins |
title_short | Actin activates Pseudomonas aeruginosa ExoY nucleotidyl cyclase toxin and ExoY-like effector domains from MARTX toxins |
title_sort | actin activates pseudomonas aeruginosa exoy nucleotidyl cyclase toxin and exoy-like effector domains from martx toxins |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5150216/ https://www.ncbi.nlm.nih.gov/pubmed/27917880 http://dx.doi.org/10.1038/ncomms13582 |
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