Cargando…

Bacillus cereus non-haemolytic enterotoxin activates the NLRP3 inflammasome

Inflammasomes are important for host defence against pathogens and homeostasis with commensal microbes. Here, we show non-haemolytic enterotoxin (NHE) from the neglected human foodborne pathogen Bacillus cereus is an activator of the NLRP3 inflammasome and pyroptosis. NHE is a non-redundant toxin to...

Descripción completa

Detalles Bibliográficos
Autores principales: Fox, Daniel, Mathur, Anukriti, Xue, Yansong, Liu, Yunqi, Tan, Wei Hong, Feng, Shouya, Pandey, Abhimanu, Ngo, Chinh, Hayward, Jenni A., Atmosukarto, Ines I., Price, Jason D., Johnson, Matthew D., Jessberger, Nadja, Robertson, Avril A. B., Burgio, Gaetan, Tscharke, David C., Fox, Edward M., Leyton, Denisse L., Kaakoush, Nadeem O., Märtlbauer, Erwin, Leppla, Stephen H., Man, Si Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005308/
https://www.ncbi.nlm.nih.gov/pubmed/32029733
http://dx.doi.org/10.1038/s41467-020-14534-3
_version_ 1783494908579938304
author Fox, Daniel
Mathur, Anukriti
Xue, Yansong
Liu, Yunqi
Tan, Wei Hong
Feng, Shouya
Pandey, Abhimanu
Ngo, Chinh
Hayward, Jenni A.
Atmosukarto, Ines I.
Price, Jason D.
Johnson, Matthew D.
Jessberger, Nadja
Robertson, Avril A. B.
Burgio, Gaetan
Tscharke, David C.
Fox, Edward M.
Leyton, Denisse L.
Kaakoush, Nadeem O.
Märtlbauer, Erwin
Leppla, Stephen H.
Man, Si Ming
author_facet Fox, Daniel
Mathur, Anukriti
Xue, Yansong
Liu, Yunqi
Tan, Wei Hong
Feng, Shouya
Pandey, Abhimanu
Ngo, Chinh
Hayward, Jenni A.
Atmosukarto, Ines I.
Price, Jason D.
Johnson, Matthew D.
Jessberger, Nadja
Robertson, Avril A. B.
Burgio, Gaetan
Tscharke, David C.
Fox, Edward M.
Leyton, Denisse L.
Kaakoush, Nadeem O.
Märtlbauer, Erwin
Leppla, Stephen H.
Man, Si Ming
author_sort Fox, Daniel
collection PubMed
description Inflammasomes are important for host defence against pathogens and homeostasis with commensal microbes. Here, we show non-haemolytic enterotoxin (NHE) from the neglected human foodborne pathogen Bacillus cereus is an activator of the NLRP3 inflammasome and pyroptosis. NHE is a non-redundant toxin to haemolysin BL (HBL) despite having a similar mechanism of action. Via a putative transmembrane region, subunit C of NHE initiates binding to the plasma membrane, leading to the recruitment of subunit B and subunit A, thus forming a tripartite lytic pore that is permissive to efflux of potassium. NHE mediates killing of cells from multiple lineages and hosts, highlighting a versatile functional repertoire in different host species. These data indicate that NHE and HBL operate synergistically to induce inflammation and show that multiple virulence factors from the same pathogen with conserved function and mechanism of action can be exploited for sensing by a single inflammasome.
format Online
Article
Text
id pubmed-7005308
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-70053082020-02-10 Bacillus cereus non-haemolytic enterotoxin activates the NLRP3 inflammasome Fox, Daniel Mathur, Anukriti Xue, Yansong Liu, Yunqi Tan, Wei Hong Feng, Shouya Pandey, Abhimanu Ngo, Chinh Hayward, Jenni A. Atmosukarto, Ines I. Price, Jason D. Johnson, Matthew D. Jessberger, Nadja Robertson, Avril A. B. Burgio, Gaetan Tscharke, David C. Fox, Edward M. Leyton, Denisse L. Kaakoush, Nadeem O. Märtlbauer, Erwin Leppla, Stephen H. Man, Si Ming Nat Commun Article Inflammasomes are important for host defence against pathogens and homeostasis with commensal microbes. Here, we show non-haemolytic enterotoxin (NHE) from the neglected human foodborne pathogen Bacillus cereus is an activator of the NLRP3 inflammasome and pyroptosis. NHE is a non-redundant toxin to haemolysin BL (HBL) despite having a similar mechanism of action. Via a putative transmembrane region, subunit C of NHE initiates binding to the plasma membrane, leading to the recruitment of subunit B and subunit A, thus forming a tripartite lytic pore that is permissive to efflux of potassium. NHE mediates killing of cells from multiple lineages and hosts, highlighting a versatile functional repertoire in different host species. These data indicate that NHE and HBL operate synergistically to induce inflammation and show that multiple virulence factors from the same pathogen with conserved function and mechanism of action can be exploited for sensing by a single inflammasome. Nature Publishing Group UK 2020-02-06 /pmc/articles/PMC7005308/ /pubmed/32029733 http://dx.doi.org/10.1038/s41467-020-14534-3 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Fox, Daniel
Mathur, Anukriti
Xue, Yansong
Liu, Yunqi
Tan, Wei Hong
Feng, Shouya
Pandey, Abhimanu
Ngo, Chinh
Hayward, Jenni A.
Atmosukarto, Ines I.
Price, Jason D.
Johnson, Matthew D.
Jessberger, Nadja
Robertson, Avril A. B.
Burgio, Gaetan
Tscharke, David C.
Fox, Edward M.
Leyton, Denisse L.
Kaakoush, Nadeem O.
Märtlbauer, Erwin
Leppla, Stephen H.
Man, Si Ming
Bacillus cereus non-haemolytic enterotoxin activates the NLRP3 inflammasome
title Bacillus cereus non-haemolytic enterotoxin activates the NLRP3 inflammasome
title_full Bacillus cereus non-haemolytic enterotoxin activates the NLRP3 inflammasome
title_fullStr Bacillus cereus non-haemolytic enterotoxin activates the NLRP3 inflammasome
title_full_unstemmed Bacillus cereus non-haemolytic enterotoxin activates the NLRP3 inflammasome
title_short Bacillus cereus non-haemolytic enterotoxin activates the NLRP3 inflammasome
title_sort bacillus cereus non-haemolytic enterotoxin activates the nlrp3 inflammasome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005308/
https://www.ncbi.nlm.nih.gov/pubmed/32029733
http://dx.doi.org/10.1038/s41467-020-14534-3
work_keys_str_mv AT foxdaniel bacilluscereusnonhaemolyticenterotoxinactivatesthenlrp3inflammasome
AT mathuranukriti bacilluscereusnonhaemolyticenterotoxinactivatesthenlrp3inflammasome
AT xueyansong bacilluscereusnonhaemolyticenterotoxinactivatesthenlrp3inflammasome
AT liuyunqi bacilluscereusnonhaemolyticenterotoxinactivatesthenlrp3inflammasome
AT tanweihong bacilluscereusnonhaemolyticenterotoxinactivatesthenlrp3inflammasome
AT fengshouya bacilluscereusnonhaemolyticenterotoxinactivatesthenlrp3inflammasome
AT pandeyabhimanu bacilluscereusnonhaemolyticenterotoxinactivatesthenlrp3inflammasome
AT ngochinh bacilluscereusnonhaemolyticenterotoxinactivatesthenlrp3inflammasome
AT haywardjennia bacilluscereusnonhaemolyticenterotoxinactivatesthenlrp3inflammasome
AT atmosukartoinesi bacilluscereusnonhaemolyticenterotoxinactivatesthenlrp3inflammasome
AT pricejasond bacilluscereusnonhaemolyticenterotoxinactivatesthenlrp3inflammasome
AT johnsonmatthewd bacilluscereusnonhaemolyticenterotoxinactivatesthenlrp3inflammasome
AT jessbergernadja bacilluscereusnonhaemolyticenterotoxinactivatesthenlrp3inflammasome
AT robertsonavrilab bacilluscereusnonhaemolyticenterotoxinactivatesthenlrp3inflammasome
AT burgiogaetan bacilluscereusnonhaemolyticenterotoxinactivatesthenlrp3inflammasome
AT tscharkedavidc bacilluscereusnonhaemolyticenterotoxinactivatesthenlrp3inflammasome
AT foxedwardm bacilluscereusnonhaemolyticenterotoxinactivatesthenlrp3inflammasome
AT leytondenissel bacilluscereusnonhaemolyticenterotoxinactivatesthenlrp3inflammasome
AT kaakoushnadeemo bacilluscereusnonhaemolyticenterotoxinactivatesthenlrp3inflammasome
AT martlbauererwin bacilluscereusnonhaemolyticenterotoxinactivatesthenlrp3inflammasome
AT lepplastephenh bacilluscereusnonhaemolyticenterotoxinactivatesthenlrp3inflammasome
AT mansiming bacilluscereusnonhaemolyticenterotoxinactivatesthenlrp3inflammasome