The Pseudomonas aeruginosa Type VI Secretion PGAP1-like Effector Induces Host Autophagy by Activating Endoplasmic Reticulum Stress

Pseudomonas aeruginosa is an opportunistic pathogen that regularly causes nosocomial infections in hospitalized patients. The type VI secretion system (T6SS) is responsible for the secretion of numerous virulence effector proteins that can both interfere with competing microbes and manipulate host c...

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Main Authors: Feng Jiang, Xia Wang, Bei Wang, Lihong Chen, Zhendong Zhao, Nicholas R. Waterfield, Guowei Yang, Qi Jin
Format: Article
Language:English
Published: Elsevier 2016-08-01
Series:Cell Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124716308981
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spelling doaj-c800018f557b440b8c0ffcec036be36d2020-11-25T01:52:32ZengElsevierCell Reports2211-12472016-08-011661502150910.1016/j.celrep.2016.07.012The Pseudomonas aeruginosa Type VI Secretion PGAP1-like Effector Induces Host Autophagy by Activating Endoplasmic Reticulum StressFeng Jiang0Xia Wang1Bei Wang2Lihong Chen3Zhendong Zhao4Nicholas R. Waterfield5Guowei Yang6Qi Jin7MOH Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, 6 Rong Jing Dong Jie, Beijing 100176, P.R. ChinaMOH Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, 6 Rong Jing Dong Jie, Beijing 100176, P.R. ChinaMOH Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, 6 Rong Jing Dong Jie, Beijing 100176, P.R. ChinaMOH Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, 6 Rong Jing Dong Jie, Beijing 100176, P.R. ChinaMOH Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, 6 Rong Jing Dong Jie, Beijing 100176, P.R. ChinaDivision of Biomedical Science, Warwick Medical School, Warwick University, Coventry CV4 7AL, UKMOH Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, 6 Rong Jing Dong Jie, Beijing 100176, P.R. ChinaMOH Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, 6 Rong Jing Dong Jie, Beijing 100176, P.R. ChinaPseudomonas aeruginosa is an opportunistic pathogen that regularly causes nosocomial infections in hospitalized patients. The type VI secretion system (T6SS) is responsible for the secretion of numerous virulence effector proteins that can both interfere with competing microbes and manipulate host cells. Here, we report a detailed investigation of a P. aeruginosa H2-T6SS-dependent phospholipase effector, TplE, which acts as a trans-kingdom toxin. Delivery of TplE to the periplasmic space of rival bacteria leads to growth inhibition. Importantly, TplE, also contains a eukaryotic PGAP1-like domain, which targets the host ER apparatus, ultimately leading to disruption of the ER. TplE activity leads to the activation of the unfolded protein response (UPR) through the IRE1α-XBP1 pathway, enhancing autophagic flux. These findings indicate that this T6SS-delivered phospholipase effector is active against both prokaryotic and eukaryotic cellular targets, highlighting the T6SS as a versatile weapon in the Pseudomonas arsenal.http://www.sciencedirect.com/science/article/pii/S2211124716308981
collection DOAJ
language English
format Article
sources DOAJ
author Feng Jiang
Xia Wang
Bei Wang
Lihong Chen
Zhendong Zhao
Nicholas R. Waterfield
Guowei Yang
Qi Jin
spellingShingle Feng Jiang
Xia Wang
Bei Wang
Lihong Chen
Zhendong Zhao
Nicholas R. Waterfield
Guowei Yang
Qi Jin
The Pseudomonas aeruginosa Type VI Secretion PGAP1-like Effector Induces Host Autophagy by Activating Endoplasmic Reticulum Stress
Cell Reports
author_facet Feng Jiang
Xia Wang
Bei Wang
Lihong Chen
Zhendong Zhao
Nicholas R. Waterfield
Guowei Yang
Qi Jin
author_sort Feng Jiang
title The Pseudomonas aeruginosa Type VI Secretion PGAP1-like Effector Induces Host Autophagy by Activating Endoplasmic Reticulum Stress
title_short The Pseudomonas aeruginosa Type VI Secretion PGAP1-like Effector Induces Host Autophagy by Activating Endoplasmic Reticulum Stress
title_full The Pseudomonas aeruginosa Type VI Secretion PGAP1-like Effector Induces Host Autophagy by Activating Endoplasmic Reticulum Stress
title_fullStr The Pseudomonas aeruginosa Type VI Secretion PGAP1-like Effector Induces Host Autophagy by Activating Endoplasmic Reticulum Stress
title_full_unstemmed The Pseudomonas aeruginosa Type VI Secretion PGAP1-like Effector Induces Host Autophagy by Activating Endoplasmic Reticulum Stress
title_sort pseudomonas aeruginosa type vi secretion pgap1-like effector induces host autophagy by activating endoplasmic reticulum stress
publisher Elsevier
series Cell Reports
issn 2211-1247
publishDate 2016-08-01
description Pseudomonas aeruginosa is an opportunistic pathogen that regularly causes nosocomial infections in hospitalized patients. The type VI secretion system (T6SS) is responsible for the secretion of numerous virulence effector proteins that can both interfere with competing microbes and manipulate host cells. Here, we report a detailed investigation of a P. aeruginosa H2-T6SS-dependent phospholipase effector, TplE, which acts as a trans-kingdom toxin. Delivery of TplE to the periplasmic space of rival bacteria leads to growth inhibition. Importantly, TplE, also contains a eukaryotic PGAP1-like domain, which targets the host ER apparatus, ultimately leading to disruption of the ER. TplE activity leads to the activation of the unfolded protein response (UPR) through the IRE1α-XBP1 pathway, enhancing autophagic flux. These findings indicate that this T6SS-delivered phospholipase effector is active against both prokaryotic and eukaryotic cellular targets, highlighting the T6SS as a versatile weapon in the Pseudomonas arsenal.
url http://www.sciencedirect.com/science/article/pii/S2211124716308981
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