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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Taylor & Francis
2017
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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 |
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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 |
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