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Flagellar Motility Is Critical for Salmonella enterica Serovar Typhimurium Biofilm Development

The food-borne pathogen Salmonella enterica serovar Typhimurium (S. Typhimurium) causes self-limiting gastroenteritis in humans and is not easily eradicated because it often attaches to suitable surfaces to form biofilms that have high resistance to disinfectants and antimicrobials. To develop an al...

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Autores principales: Wang, Feiying, Deng, Le, Huang, Fangfang, Wang, Zefeng, Lu, Qiujun, Xu, Chenran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7509047/
https://www.ncbi.nlm.nih.gov/pubmed/33013719
http://dx.doi.org/10.3389/fmicb.2020.01695
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author Wang, Feiying
Deng, Le
Huang, Fangfang
Wang, Zefeng
Lu, Qiujun
Xu, Chenran
author_facet Wang, Feiying
Deng, Le
Huang, Fangfang
Wang, Zefeng
Lu, Qiujun
Xu, Chenran
author_sort Wang, Feiying
collection PubMed
description The food-borne pathogen Salmonella enterica serovar Typhimurium (S. Typhimurium) causes self-limiting gastroenteritis in humans and is not easily eradicated because it often attaches to suitable surfaces to form biofilms that have high resistance to disinfectants and antimicrobials. To develop an alternative strategy for the treatment of biofilms, it is necessary to further explore the effects of flagellar motility on the development process of Salmonella biofilms. Here, we constructed flagella mutants (ΔflgE and ΔfliC) to systematically study this process. By comparing them with wild-type strains, we found that these mutants lacking flagellar motility form fewer biofilms in the early stage, and the formed mature biofilms contain more cells and extracellular polymeric substances (EPS). In addition, fewer mutant cells adhered to glass plates compared with wild-type cells even after 6 h of incubation, suggesting that flagellar motility plays a significant role in preliminary cell-surface interactions. More importantly, the motility of wild-type strain was greatly decreased when they were treated with carbonyl cyanide m-chlorophenylhydrazone, which inhibited flagellar motility and reduced biofilm formation, as in the case of the ΔflgE mutant. Overall, these findings suggest that flagellar motility plays an important role in Salmonella biofilm initiation and maturation, which can help us to counteract the mechanisms involved in biofilm formation and to develop more rational control strategies.
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spelling pubmed-75090472020-10-02 Flagellar Motility Is Critical for Salmonella enterica Serovar Typhimurium Biofilm Development Wang, Feiying Deng, Le Huang, Fangfang Wang, Zefeng Lu, Qiujun Xu, Chenran Front Microbiol Microbiology The food-borne pathogen Salmonella enterica serovar Typhimurium (S. Typhimurium) causes self-limiting gastroenteritis in humans and is not easily eradicated because it often attaches to suitable surfaces to form biofilms that have high resistance to disinfectants and antimicrobials. To develop an alternative strategy for the treatment of biofilms, it is necessary to further explore the effects of flagellar motility on the development process of Salmonella biofilms. Here, we constructed flagella mutants (ΔflgE and ΔfliC) to systematically study this process. By comparing them with wild-type strains, we found that these mutants lacking flagellar motility form fewer biofilms in the early stage, and the formed mature biofilms contain more cells and extracellular polymeric substances (EPS). In addition, fewer mutant cells adhered to glass plates compared with wild-type cells even after 6 h of incubation, suggesting that flagellar motility plays a significant role in preliminary cell-surface interactions. More importantly, the motility of wild-type strain was greatly decreased when they were treated with carbonyl cyanide m-chlorophenylhydrazone, which inhibited flagellar motility and reduced biofilm formation, as in the case of the ΔflgE mutant. Overall, these findings suggest that flagellar motility plays an important role in Salmonella biofilm initiation and maturation, which can help us to counteract the mechanisms involved in biofilm formation and to develop more rational control strategies. Frontiers Media S.A. 2020-09-09 /pmc/articles/PMC7509047/ /pubmed/33013719 http://dx.doi.org/10.3389/fmicb.2020.01695 Text en Copyright © 2020 Wang, Deng, Huang, Wang, Lu and Xu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Wang, Feiying
Deng, Le
Huang, Fangfang
Wang, Zefeng
Lu, Qiujun
Xu, Chenran
Flagellar Motility Is Critical for Salmonella enterica Serovar Typhimurium Biofilm Development
title Flagellar Motility Is Critical for Salmonella enterica Serovar Typhimurium Biofilm Development
title_full Flagellar Motility Is Critical for Salmonella enterica Serovar Typhimurium Biofilm Development
title_fullStr Flagellar Motility Is Critical for Salmonella enterica Serovar Typhimurium Biofilm Development
title_full_unstemmed Flagellar Motility Is Critical for Salmonella enterica Serovar Typhimurium Biofilm Development
title_short Flagellar Motility Is Critical for Salmonella enterica Serovar Typhimurium Biofilm Development
title_sort flagellar motility is critical for salmonella enterica serovar typhimurium biofilm development
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7509047/
https://www.ncbi.nlm.nih.gov/pubmed/33013719
http://dx.doi.org/10.3389/fmicb.2020.01695
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