Cargando…

Nitrate Is an Environmental Cue in the Gut for Salmonella enterica Serovar Typhimurium Biofilm Dispersal through Curli Repression and Flagellum Activation via Cyclic-di-GMP Signaling

Curli, a major component of the bacterial biofilms in the intestinal tract, activates pattern recognition receptors and triggers joint inflammation after infection with Salmonella enterica serovar Typhimurium. The factors that allow S. Typhimurium to disperse from biofilms and invade the epithelium...

Descripción completa

Detalles Bibliográficos
Autores principales: Miller, Amanda L., Nicastro, Lauren K., Bessho, Shingo, Grando, Kaitlyn, White, Aaron P., Zhang, Yi, Queisser, Gillian, Buttaro, Bettina A., Tükel, Çagla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8822344/
https://www.ncbi.nlm.nih.gov/pubmed/35130730
http://dx.doi.org/10.1128/mbio.02886-21
_version_ 1784646588225814528
author Miller, Amanda L.
Nicastro, Lauren K.
Bessho, Shingo
Grando, Kaitlyn
White, Aaron P.
Zhang, Yi
Queisser, Gillian
Buttaro, Bettina A.
Tükel, Çagla
author_facet Miller, Amanda L.
Nicastro, Lauren K.
Bessho, Shingo
Grando, Kaitlyn
White, Aaron P.
Zhang, Yi
Queisser, Gillian
Buttaro, Bettina A.
Tükel, Çagla
author_sort Miller, Amanda L.
collection PubMed
description Curli, a major component of the bacterial biofilms in the intestinal tract, activates pattern recognition receptors and triggers joint inflammation after infection with Salmonella enterica serovar Typhimurium. The factors that allow S. Typhimurium to disperse from biofilms and invade the epithelium to establish a successful infection during acute inflammation remain unknown. Here, we studied S. Typhimurium biofilms in vitro and in vivo to understand how the inflammatory environment regulates the switch between multicellular and motile S. Typhimurium in the gut. We discovered that nitrate generated by the host is an environmental cue that induces S. Typhimurium to disperse from the biofilm. Nitrate represses production of an important biofilm component, curli, and activates flagella via the modulation of intracellular cyclic-di-GMP levels. We conclude that nitrate plays a central role in pathogen fitness by regulating the sessile-to-motile lifestyle switch during infection.
format Online
Article
Text
id pubmed-8822344
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-88223442022-02-17 Nitrate Is an Environmental Cue in the Gut for Salmonella enterica Serovar Typhimurium Biofilm Dispersal through Curli Repression and Flagellum Activation via Cyclic-di-GMP Signaling Miller, Amanda L. Nicastro, Lauren K. Bessho, Shingo Grando, Kaitlyn White, Aaron P. Zhang, Yi Queisser, Gillian Buttaro, Bettina A. Tükel, Çagla mBio Research Article Curli, a major component of the bacterial biofilms in the intestinal tract, activates pattern recognition receptors and triggers joint inflammation after infection with Salmonella enterica serovar Typhimurium. The factors that allow S. Typhimurium to disperse from biofilms and invade the epithelium to establish a successful infection during acute inflammation remain unknown. Here, we studied S. Typhimurium biofilms in vitro and in vivo to understand how the inflammatory environment regulates the switch between multicellular and motile S. Typhimurium in the gut. We discovered that nitrate generated by the host is an environmental cue that induces S. Typhimurium to disperse from the biofilm. Nitrate represses production of an important biofilm component, curli, and activates flagella via the modulation of intracellular cyclic-di-GMP levels. We conclude that nitrate plays a central role in pathogen fitness by regulating the sessile-to-motile lifestyle switch during infection. American Society for Microbiology 2022-02-08 /pmc/articles/PMC8822344/ /pubmed/35130730 http://dx.doi.org/10.1128/mbio.02886-21 Text en Copyright © 2022 Miller et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Miller, Amanda L.
Nicastro, Lauren K.
Bessho, Shingo
Grando, Kaitlyn
White, Aaron P.
Zhang, Yi
Queisser, Gillian
Buttaro, Bettina A.
Tükel, Çagla
Nitrate Is an Environmental Cue in the Gut for Salmonella enterica Serovar Typhimurium Biofilm Dispersal through Curli Repression and Flagellum Activation via Cyclic-di-GMP Signaling
title Nitrate Is an Environmental Cue in the Gut for Salmonella enterica Serovar Typhimurium Biofilm Dispersal through Curli Repression and Flagellum Activation via Cyclic-di-GMP Signaling
title_full Nitrate Is an Environmental Cue in the Gut for Salmonella enterica Serovar Typhimurium Biofilm Dispersal through Curli Repression and Flagellum Activation via Cyclic-di-GMP Signaling
title_fullStr Nitrate Is an Environmental Cue in the Gut for Salmonella enterica Serovar Typhimurium Biofilm Dispersal through Curli Repression and Flagellum Activation via Cyclic-di-GMP Signaling
title_full_unstemmed Nitrate Is an Environmental Cue in the Gut for Salmonella enterica Serovar Typhimurium Biofilm Dispersal through Curli Repression and Flagellum Activation via Cyclic-di-GMP Signaling
title_short Nitrate Is an Environmental Cue in the Gut for Salmonella enterica Serovar Typhimurium Biofilm Dispersal through Curli Repression and Flagellum Activation via Cyclic-di-GMP Signaling
title_sort nitrate is an environmental cue in the gut for salmonella enterica serovar typhimurium biofilm dispersal through curli repression and flagellum activation via cyclic-di-gmp signaling
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8822344/
https://www.ncbi.nlm.nih.gov/pubmed/35130730
http://dx.doi.org/10.1128/mbio.02886-21
work_keys_str_mv AT milleramandal nitrateisanenvironmentalcueinthegutforsalmonellaentericaserovartyphimuriumbiofilmdispersalthroughcurlirepressionandflagellumactivationviacyclicdigmpsignaling
AT nicastrolaurenk nitrateisanenvironmentalcueinthegutforsalmonellaentericaserovartyphimuriumbiofilmdispersalthroughcurlirepressionandflagellumactivationviacyclicdigmpsignaling
AT besshoshingo nitrateisanenvironmentalcueinthegutforsalmonellaentericaserovartyphimuriumbiofilmdispersalthroughcurlirepressionandflagellumactivationviacyclicdigmpsignaling
AT grandokaitlyn nitrateisanenvironmentalcueinthegutforsalmonellaentericaserovartyphimuriumbiofilmdispersalthroughcurlirepressionandflagellumactivationviacyclicdigmpsignaling
AT whiteaaronp nitrateisanenvironmentalcueinthegutforsalmonellaentericaserovartyphimuriumbiofilmdispersalthroughcurlirepressionandflagellumactivationviacyclicdigmpsignaling
AT zhangyi nitrateisanenvironmentalcueinthegutforsalmonellaentericaserovartyphimuriumbiofilmdispersalthroughcurlirepressionandflagellumactivationviacyclicdigmpsignaling
AT queissergillian nitrateisanenvironmentalcueinthegutforsalmonellaentericaserovartyphimuriumbiofilmdispersalthroughcurlirepressionandflagellumactivationviacyclicdigmpsignaling
AT buttarobettinaa nitrateisanenvironmentalcueinthegutforsalmonellaentericaserovartyphimuriumbiofilmdispersalthroughcurlirepressionandflagellumactivationviacyclicdigmpsignaling
AT tukelcagla nitrateisanenvironmentalcueinthegutforsalmonellaentericaserovartyphimuriumbiofilmdispersalthroughcurlirepressionandflagellumactivationviacyclicdigmpsignaling