Cargando…

Intracellular bacteria engage a STING-TBK1-MVB12b pathway to enable paracrine cGAS-STING signaling

The innate immune system is crucial for eventual control of infections, but may also contribute to pathology. Listeria monocytogenes is an intracellular gram-positive bacteria and a major cause of food-borne disease. However, important knowledge on the interactions between L. monocytogenes and the i...

Descripción completa

Detalles Bibliográficos
Autores principales: Nandakumar, Ramya, Tschismarov, Roland, Meissner, Felix, Prabakaran, Thaneas, Krissanaprasit, Abhichart, Farahani, Ensieh, Zhang, Bao-cun, Assil, Sonia, Martin, Amandine, Bertrams, Wilhelm, Holm, Christian K, Ablasser, Andrea, Klause, Tanja, Thomsen, Martin K, Schmeck, Bernd, Howard, Kenneth A, Henry, Thomas, Gothelf, Kurt V, Decker, Thomas, Paludan, Søren R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6433288/
https://www.ncbi.nlm.nih.gov/pubmed/30804548
http://dx.doi.org/10.1038/s41564-019-0367-z
_version_ 1783406275308027904
author Nandakumar, Ramya
Tschismarov, Roland
Meissner, Felix
Prabakaran, Thaneas
Krissanaprasit, Abhichart
Farahani, Ensieh
Zhang, Bao-cun
Assil, Sonia
Martin, Amandine
Bertrams, Wilhelm
Holm, Christian K
Ablasser, Andrea
Klause, Tanja
Thomsen, Martin K
Schmeck, Bernd
Howard, Kenneth A
Henry, Thomas
Gothelf, Kurt V
Decker, Thomas
Paludan, Søren R
author_facet Nandakumar, Ramya
Tschismarov, Roland
Meissner, Felix
Prabakaran, Thaneas
Krissanaprasit, Abhichart
Farahani, Ensieh
Zhang, Bao-cun
Assil, Sonia
Martin, Amandine
Bertrams, Wilhelm
Holm, Christian K
Ablasser, Andrea
Klause, Tanja
Thomsen, Martin K
Schmeck, Bernd
Howard, Kenneth A
Henry, Thomas
Gothelf, Kurt V
Decker, Thomas
Paludan, Søren R
author_sort Nandakumar, Ramya
collection PubMed
description The innate immune system is crucial for eventual control of infections, but may also contribute to pathology. Listeria monocytogenes is an intracellular gram-positive bacteria and a major cause of food-borne disease. However, important knowledge on the interactions between L. monocytogenes and the immune system is still missing. Here we report that Listeria DNA is sorted into extracellular vesicles (EV)s in infected cells and delivered to bystander cells to stimulate the cGAS-STING pathway. This was also observed during infections with Francisella tularensis and Legionella pneumophila. We identify the multivesicular body protein MVB12b as a target for TBK1 phosphorylation, which is essential for sorting of DNA into EVs and stimulation of bystander cells. EVs from Listeria-infected cells inhibited T cell proliferation, and primed T cells for apoptosis. Collectively, we describe a pathway for EV-mediated delivery of foreign DNA to bystander cells, and suggest that intracellular bacteria exploit this pathway to impair anti-bacterial defense.
format Online
Article
Text
id pubmed-6433288
institution National Center for Biotechnology Information
language English
publishDate 2019
record_format MEDLINE/PubMed
spelling pubmed-64332882019-08-25 Intracellular bacteria engage a STING-TBK1-MVB12b pathway to enable paracrine cGAS-STING signaling Nandakumar, Ramya Tschismarov, Roland Meissner, Felix Prabakaran, Thaneas Krissanaprasit, Abhichart Farahani, Ensieh Zhang, Bao-cun Assil, Sonia Martin, Amandine Bertrams, Wilhelm Holm, Christian K Ablasser, Andrea Klause, Tanja Thomsen, Martin K Schmeck, Bernd Howard, Kenneth A Henry, Thomas Gothelf, Kurt V Decker, Thomas Paludan, Søren R Nat Microbiol Article The innate immune system is crucial for eventual control of infections, but may also contribute to pathology. Listeria monocytogenes is an intracellular gram-positive bacteria and a major cause of food-borne disease. However, important knowledge on the interactions between L. monocytogenes and the immune system is still missing. Here we report that Listeria DNA is sorted into extracellular vesicles (EV)s in infected cells and delivered to bystander cells to stimulate the cGAS-STING pathway. This was also observed during infections with Francisella tularensis and Legionella pneumophila. We identify the multivesicular body protein MVB12b as a target for TBK1 phosphorylation, which is essential for sorting of DNA into EVs and stimulation of bystander cells. EVs from Listeria-infected cells inhibited T cell proliferation, and primed T cells for apoptosis. Collectively, we describe a pathway for EV-mediated delivery of foreign DNA to bystander cells, and suggest that intracellular bacteria exploit this pathway to impair anti-bacterial defense. 2019-02-25 2019-04 /pmc/articles/PMC6433288/ /pubmed/30804548 http://dx.doi.org/10.1038/s41564-019-0367-z Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Nandakumar, Ramya
Tschismarov, Roland
Meissner, Felix
Prabakaran, Thaneas
Krissanaprasit, Abhichart
Farahani, Ensieh
Zhang, Bao-cun
Assil, Sonia
Martin, Amandine
Bertrams, Wilhelm
Holm, Christian K
Ablasser, Andrea
Klause, Tanja
Thomsen, Martin K
Schmeck, Bernd
Howard, Kenneth A
Henry, Thomas
Gothelf, Kurt V
Decker, Thomas
Paludan, Søren R
Intracellular bacteria engage a STING-TBK1-MVB12b pathway to enable paracrine cGAS-STING signaling
title Intracellular bacteria engage a STING-TBK1-MVB12b pathway to enable paracrine cGAS-STING signaling
title_full Intracellular bacteria engage a STING-TBK1-MVB12b pathway to enable paracrine cGAS-STING signaling
title_fullStr Intracellular bacteria engage a STING-TBK1-MVB12b pathway to enable paracrine cGAS-STING signaling
title_full_unstemmed Intracellular bacteria engage a STING-TBK1-MVB12b pathway to enable paracrine cGAS-STING signaling
title_short Intracellular bacteria engage a STING-TBK1-MVB12b pathway to enable paracrine cGAS-STING signaling
title_sort intracellular bacteria engage a sting-tbk1-mvb12b pathway to enable paracrine cgas-sting signaling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6433288/
https://www.ncbi.nlm.nih.gov/pubmed/30804548
http://dx.doi.org/10.1038/s41564-019-0367-z
work_keys_str_mv AT nandakumarramya intracellularbacteriaengageastingtbk1mvb12bpathwaytoenableparacrinecgasstingsignaling
AT tschismarovroland intracellularbacteriaengageastingtbk1mvb12bpathwaytoenableparacrinecgasstingsignaling
AT meissnerfelix intracellularbacteriaengageastingtbk1mvb12bpathwaytoenableparacrinecgasstingsignaling
AT prabakaranthaneas intracellularbacteriaengageastingtbk1mvb12bpathwaytoenableparacrinecgasstingsignaling
AT krissanaprasitabhichart intracellularbacteriaengageastingtbk1mvb12bpathwaytoenableparacrinecgasstingsignaling
AT farahaniensieh intracellularbacteriaengageastingtbk1mvb12bpathwaytoenableparacrinecgasstingsignaling
AT zhangbaocun intracellularbacteriaengageastingtbk1mvb12bpathwaytoenableparacrinecgasstingsignaling
AT assilsonia intracellularbacteriaengageastingtbk1mvb12bpathwaytoenableparacrinecgasstingsignaling
AT martinamandine intracellularbacteriaengageastingtbk1mvb12bpathwaytoenableparacrinecgasstingsignaling
AT bertramswilhelm intracellularbacteriaengageastingtbk1mvb12bpathwaytoenableparacrinecgasstingsignaling
AT holmchristiank intracellularbacteriaengageastingtbk1mvb12bpathwaytoenableparacrinecgasstingsignaling
AT ablasserandrea intracellularbacteriaengageastingtbk1mvb12bpathwaytoenableparacrinecgasstingsignaling
AT klausetanja intracellularbacteriaengageastingtbk1mvb12bpathwaytoenableparacrinecgasstingsignaling
AT thomsenmartink intracellularbacteriaengageastingtbk1mvb12bpathwaytoenableparacrinecgasstingsignaling
AT schmeckbernd intracellularbacteriaengageastingtbk1mvb12bpathwaytoenableparacrinecgasstingsignaling
AT howardkennetha intracellularbacteriaengageastingtbk1mvb12bpathwaytoenableparacrinecgasstingsignaling
AT henrythomas intracellularbacteriaengageastingtbk1mvb12bpathwaytoenableparacrinecgasstingsignaling
AT gothelfkurtv intracellularbacteriaengageastingtbk1mvb12bpathwaytoenableparacrinecgasstingsignaling
AT deckerthomas intracellularbacteriaengageastingtbk1mvb12bpathwaytoenableparacrinecgasstingsignaling
AT paludansørenr intracellularbacteriaengageastingtbk1mvb12bpathwaytoenableparacrinecgasstingsignaling