Cargando…

Chlamydia trachomatis inhibits apoptosis in infected cells by targeting the pro-apoptotic proteins Bax and Bak

Apoptosis acts in defense against microbial infection, and many infectious agents have developed strategies to inhibit host cell apoptosis. The human pathogen Chlamydia trachomatis (Ctr) is an obligate intracellular bacterium that strongly inhibits mitochondrial apoptosis of its human host cell but...

Descripción completa

Detalles Bibliográficos
Autores principales: Waguia Kontchou, Collins, Gentle, Ian E., Weber, Arnim, Schoeniger, Axel, Edlich, Frank, Häcker, Georg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9525694/
https://www.ncbi.nlm.nih.gov/pubmed/35397654
http://dx.doi.org/10.1038/s41418-022-00995-0
_version_ 1784800735855116288
author Waguia Kontchou, Collins
Gentle, Ian E.
Weber, Arnim
Schoeniger, Axel
Edlich, Frank
Häcker, Georg
author_facet Waguia Kontchou, Collins
Gentle, Ian E.
Weber, Arnim
Schoeniger, Axel
Edlich, Frank
Häcker, Georg
author_sort Waguia Kontchou, Collins
collection PubMed
description Apoptosis acts in defense against microbial infection, and many infectious agents have developed strategies to inhibit host cell apoptosis. The human pathogen Chlamydia trachomatis (Ctr) is an obligate intracellular bacterium that strongly inhibits mitochondrial apoptosis of its human host cell but there is no agreement how the bacteria achieve this. We here provide a molecular analysis of chlamydial apoptosis-inhibition in infected human cells and demonstrate that the block of apoptosis occurs during the activation of the effectors of mitochondrial apoptosis, Bak and Bax. We use small-molecule Bcl-2-family inhibitors and gene targeting to show that previous models cannot explain the anti-apoptotic effect of chlamydial infection. Although the anti-apoptotic Bcl-2-family protein Mcl-1 was strongly upregulated upon infection, Mcl-1-deficient cells and cells where Mcl-1 was pharmacologically inactivated were still protected. Ctr-infection could inhibit both Bax- and Bak-induced apoptosis. Apoptotic Bax-oligomerization and association with the outer mitochondrial membrane was reduced upon chlamydial infection. Infection further inhibited apoptosis induced conformational changes of Bak, as evidenced by changes to protease sensitivity, oligomerization and release from the mitochondrial porin VDAC2. Mitochondria isolated from Ctr-infected cells were protected against the pro-apoptotic Bcl-2-family proteins Bim and tBid but this protection was lost upon protease digestion. However, the protective effect of Ctr-infection was reduced in cells lacking the Bax/Bak-regulator VDAC2. We further found that OmpA, a porin of the outer membrane of Ctr, associated upon experimental expression with mitochondria and inhibited apoptosis, phenocopying the effect of the infection. These results identify a novel way of apoptosis inhibition, involving only the most downstream modulator of mitochondrial apoptosis and suggest that Chlamydia has a protein dedicated to the inhibition of apoptosis to secure its survival in human cells.
format Online
Article
Text
id pubmed-9525694
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-95256942022-10-02 Chlamydia trachomatis inhibits apoptosis in infected cells by targeting the pro-apoptotic proteins Bax and Bak Waguia Kontchou, Collins Gentle, Ian E. Weber, Arnim Schoeniger, Axel Edlich, Frank Häcker, Georg Cell Death Differ Article Apoptosis acts in defense against microbial infection, and many infectious agents have developed strategies to inhibit host cell apoptosis. The human pathogen Chlamydia trachomatis (Ctr) is an obligate intracellular bacterium that strongly inhibits mitochondrial apoptosis of its human host cell but there is no agreement how the bacteria achieve this. We here provide a molecular analysis of chlamydial apoptosis-inhibition in infected human cells and demonstrate that the block of apoptosis occurs during the activation of the effectors of mitochondrial apoptosis, Bak and Bax. We use small-molecule Bcl-2-family inhibitors and gene targeting to show that previous models cannot explain the anti-apoptotic effect of chlamydial infection. Although the anti-apoptotic Bcl-2-family protein Mcl-1 was strongly upregulated upon infection, Mcl-1-deficient cells and cells where Mcl-1 was pharmacologically inactivated were still protected. Ctr-infection could inhibit both Bax- and Bak-induced apoptosis. Apoptotic Bax-oligomerization and association with the outer mitochondrial membrane was reduced upon chlamydial infection. Infection further inhibited apoptosis induced conformational changes of Bak, as evidenced by changes to protease sensitivity, oligomerization and release from the mitochondrial porin VDAC2. Mitochondria isolated from Ctr-infected cells were protected against the pro-apoptotic Bcl-2-family proteins Bim and tBid but this protection was lost upon protease digestion. However, the protective effect of Ctr-infection was reduced in cells lacking the Bax/Bak-regulator VDAC2. We further found that OmpA, a porin of the outer membrane of Ctr, associated upon experimental expression with mitochondria and inhibited apoptosis, phenocopying the effect of the infection. These results identify a novel way of apoptosis inhibition, involving only the most downstream modulator of mitochondrial apoptosis and suggest that Chlamydia has a protein dedicated to the inhibition of apoptosis to secure its survival in human cells. Nature Publishing Group UK 2022-04-09 2022-10 /pmc/articles/PMC9525694/ /pubmed/35397654 http://dx.doi.org/10.1038/s41418-022-00995-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. (https://creativecommons.org/licenses/by/4.0/)
spellingShingle Article
Waguia Kontchou, Collins
Gentle, Ian E.
Weber, Arnim
Schoeniger, Axel
Edlich, Frank
Häcker, Georg
Chlamydia trachomatis inhibits apoptosis in infected cells by targeting the pro-apoptotic proteins Bax and Bak
title Chlamydia trachomatis inhibits apoptosis in infected cells by targeting the pro-apoptotic proteins Bax and Bak
title_full Chlamydia trachomatis inhibits apoptosis in infected cells by targeting the pro-apoptotic proteins Bax and Bak
title_fullStr Chlamydia trachomatis inhibits apoptosis in infected cells by targeting the pro-apoptotic proteins Bax and Bak
title_full_unstemmed Chlamydia trachomatis inhibits apoptosis in infected cells by targeting the pro-apoptotic proteins Bax and Bak
title_short Chlamydia trachomatis inhibits apoptosis in infected cells by targeting the pro-apoptotic proteins Bax and Bak
title_sort chlamydia trachomatis inhibits apoptosis in infected cells by targeting the pro-apoptotic proteins bax and bak
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9525694/
https://www.ncbi.nlm.nih.gov/pubmed/35397654
http://dx.doi.org/10.1038/s41418-022-00995-0
work_keys_str_mv AT waguiakontchoucollins chlamydiatrachomatisinhibitsapoptosisininfectedcellsbytargetingtheproapoptoticproteinsbaxandbak
AT gentleiane chlamydiatrachomatisinhibitsapoptosisininfectedcellsbytargetingtheproapoptoticproteinsbaxandbak
AT weberarnim chlamydiatrachomatisinhibitsapoptosisininfectedcellsbytargetingtheproapoptoticproteinsbaxandbak
AT schoenigeraxel chlamydiatrachomatisinhibitsapoptosisininfectedcellsbytargetingtheproapoptoticproteinsbaxandbak
AT edlichfrank chlamydiatrachomatisinhibitsapoptosisininfectedcellsbytargetingtheproapoptoticproteinsbaxandbak
AT hackergeorg chlamydiatrachomatisinhibitsapoptosisininfectedcellsbytargetingtheproapoptoticproteinsbaxandbak