Cargando…

The E3 ubiquitin ligase NEDD4 enhances killing of membrane-perturbing intracellular bacteria by promoting autophagy

The E3 ubiquitin ligase NEDD4 has been intensively studied in processes involved in viral infections, such as virus budding. However, little is known about its functions in bacterial infections. Our investigations into the role of NEDD4 in intracellular bacterial infections demonstrate that Mycobact...

Descripción completa

Detalles Bibliográficos
Autores principales: Pei, Gang, Buijze, Hellen, Liu, Haipeng, Moura-Alves, Pedro, Goosmann, Christian, Brinkmann, Volker, Kawabe, Hiroshi, Dorhoi, Anca, Kaufmann, Stefan H. E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5788543/
https://www.ncbi.nlm.nih.gov/pubmed/29251248
http://dx.doi.org/10.1080/15548627.2017.1376160
_version_ 1783296097063534592
author Pei, Gang
Buijze, Hellen
Liu, Haipeng
Moura-Alves, Pedro
Goosmann, Christian
Brinkmann, Volker
Kawabe, Hiroshi
Dorhoi, Anca
Kaufmann, Stefan H. E.
author_facet Pei, Gang
Buijze, Hellen
Liu, Haipeng
Moura-Alves, Pedro
Goosmann, Christian
Brinkmann, Volker
Kawabe, Hiroshi
Dorhoi, Anca
Kaufmann, Stefan H. E.
author_sort Pei, Gang
collection PubMed
description The E3 ubiquitin ligase NEDD4 has been intensively studied in processes involved in viral infections, such as virus budding. However, little is known about its functions in bacterial infections. Our investigations into the role of NEDD4 in intracellular bacterial infections demonstrate that Mycobacterium tuberculosis and Listeria monocytogenes, but not Mycobacterium bovis BCG, replicate more efficiently in NEDD4 knockdown macrophages. In parallel, NEDD4 knockdown or knockout impaired basal macroautophagy/autophagy, as well as infection-induced autophagy. Conversely, NEDD4 expression promoted autophagy in an E3 catalytic activity-dependent manner, thereby restricting intracellular Listeria replication. Mechanistic studies uncovered that endogenous NEDD4 interacted with BECN1/Beclin 1 and this interaction increased during Listeria infection. Deficiency of NEDD4 resulted in elevated K48-linkage ubiquitination of endogenous BECN1. Further, NEDD4 mediated K6- and K27- linkage ubiquitination of BECN1, leading to elevated stability of BECN1 and increased autophagy. Thus, NEDD4 participates in killing of intracellular bacterial pathogens via autophagy by sustaining the stability of BECN1.
format Online
Article
Text
id pubmed-5788543
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Taylor & Francis
record_format MEDLINE/PubMed
spelling pubmed-57885432018-02-01 The E3 ubiquitin ligase NEDD4 enhances killing of membrane-perturbing intracellular bacteria by promoting autophagy Pei, Gang Buijze, Hellen Liu, Haipeng Moura-Alves, Pedro Goosmann, Christian Brinkmann, Volker Kawabe, Hiroshi Dorhoi, Anca Kaufmann, Stefan H. E. Autophagy Research Paper-Basic Science The E3 ubiquitin ligase NEDD4 has been intensively studied in processes involved in viral infections, such as virus budding. However, little is known about its functions in bacterial infections. Our investigations into the role of NEDD4 in intracellular bacterial infections demonstrate that Mycobacterium tuberculosis and Listeria monocytogenes, but not Mycobacterium bovis BCG, replicate more efficiently in NEDD4 knockdown macrophages. In parallel, NEDD4 knockdown or knockout impaired basal macroautophagy/autophagy, as well as infection-induced autophagy. Conversely, NEDD4 expression promoted autophagy in an E3 catalytic activity-dependent manner, thereby restricting intracellular Listeria replication. Mechanistic studies uncovered that endogenous NEDD4 interacted with BECN1/Beclin 1 and this interaction increased during Listeria infection. Deficiency of NEDD4 resulted in elevated K48-linkage ubiquitination of endogenous BECN1. Further, NEDD4 mediated K6- and K27- linkage ubiquitination of BECN1, leading to elevated stability of BECN1 and increased autophagy. Thus, NEDD4 participates in killing of intracellular bacterial pathogens via autophagy by sustaining the stability of BECN1. Taylor & Francis 2017-12-17 /pmc/articles/PMC5788543/ /pubmed/29251248 http://dx.doi.org/10.1080/15548627.2017.1376160 Text en © 2017 Max Planck Institute for Infection Biology http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Research Paper-Basic Science
Pei, Gang
Buijze, Hellen
Liu, Haipeng
Moura-Alves, Pedro
Goosmann, Christian
Brinkmann, Volker
Kawabe, Hiroshi
Dorhoi, Anca
Kaufmann, Stefan H. E.
The E3 ubiquitin ligase NEDD4 enhances killing of membrane-perturbing intracellular bacteria by promoting autophagy
title The E3 ubiquitin ligase NEDD4 enhances killing of membrane-perturbing intracellular bacteria by promoting autophagy
title_full The E3 ubiquitin ligase NEDD4 enhances killing of membrane-perturbing intracellular bacteria by promoting autophagy
title_fullStr The E3 ubiquitin ligase NEDD4 enhances killing of membrane-perturbing intracellular bacteria by promoting autophagy
title_full_unstemmed The E3 ubiquitin ligase NEDD4 enhances killing of membrane-perturbing intracellular bacteria by promoting autophagy
title_short The E3 ubiquitin ligase NEDD4 enhances killing of membrane-perturbing intracellular bacteria by promoting autophagy
title_sort e3 ubiquitin ligase nedd4 enhances killing of membrane-perturbing intracellular bacteria by promoting autophagy
topic Research Paper-Basic Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5788543/
https://www.ncbi.nlm.nih.gov/pubmed/29251248
http://dx.doi.org/10.1080/15548627.2017.1376160
work_keys_str_mv AT peigang thee3ubiquitinligasenedd4enhanceskillingofmembraneperturbingintracellularbacteriabypromotingautophagy
AT buijzehellen thee3ubiquitinligasenedd4enhanceskillingofmembraneperturbingintracellularbacteriabypromotingautophagy
AT liuhaipeng thee3ubiquitinligasenedd4enhanceskillingofmembraneperturbingintracellularbacteriabypromotingautophagy
AT mouraalvespedro thee3ubiquitinligasenedd4enhanceskillingofmembraneperturbingintracellularbacteriabypromotingautophagy
AT goosmannchristian thee3ubiquitinligasenedd4enhanceskillingofmembraneperturbingintracellularbacteriabypromotingautophagy
AT brinkmannvolker thee3ubiquitinligasenedd4enhanceskillingofmembraneperturbingintracellularbacteriabypromotingautophagy
AT kawabehiroshi thee3ubiquitinligasenedd4enhanceskillingofmembraneperturbingintracellularbacteriabypromotingautophagy
AT dorhoianca thee3ubiquitinligasenedd4enhanceskillingofmembraneperturbingintracellularbacteriabypromotingautophagy
AT kaufmannstefanhe thee3ubiquitinligasenedd4enhanceskillingofmembraneperturbingintracellularbacteriabypromotingautophagy
AT peigang e3ubiquitinligasenedd4enhanceskillingofmembraneperturbingintracellularbacteriabypromotingautophagy
AT buijzehellen e3ubiquitinligasenedd4enhanceskillingofmembraneperturbingintracellularbacteriabypromotingautophagy
AT liuhaipeng e3ubiquitinligasenedd4enhanceskillingofmembraneperturbingintracellularbacteriabypromotingautophagy
AT mouraalvespedro e3ubiquitinligasenedd4enhanceskillingofmembraneperturbingintracellularbacteriabypromotingautophagy
AT goosmannchristian e3ubiquitinligasenedd4enhanceskillingofmembraneperturbingintracellularbacteriabypromotingautophagy
AT brinkmannvolker e3ubiquitinligasenedd4enhanceskillingofmembraneperturbingintracellularbacteriabypromotingautophagy
AT kawabehiroshi e3ubiquitinligasenedd4enhanceskillingofmembraneperturbingintracellularbacteriabypromotingautophagy
AT dorhoianca e3ubiquitinligasenedd4enhanceskillingofmembraneperturbingintracellularbacteriabypromotingautophagy
AT kaufmannstefanhe e3ubiquitinligasenedd4enhanceskillingofmembraneperturbingintracellularbacteriabypromotingautophagy