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Molecular Characterization of Three Tandemly Located Flagellin Genes of Stenotrophomonas maltophilia

Stenotrophomonas maltophilia is a motile, opportunistic pathogen. The flagellum, which is involved in swimming, swarming, adhesion, and biofilm formation, is considered a virulence factor for motile pathogens. Three flagellin genes, fliC1, fliC2, and fliC3, were identified from the sequenced S. malt...

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Autores principales: Wu, Cheng-Mu, Huang, Hsin-Hui, Li, Li-Hua, Lin, Yi-Tsung, Yang, Tsuey-Ching
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8998449/
https://www.ncbi.nlm.nih.gov/pubmed/35409223
http://dx.doi.org/10.3390/ijms23073863
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author Wu, Cheng-Mu
Huang, Hsin-Hui
Li, Li-Hua
Lin, Yi-Tsung
Yang, Tsuey-Ching
author_facet Wu, Cheng-Mu
Huang, Hsin-Hui
Li, Li-Hua
Lin, Yi-Tsung
Yang, Tsuey-Ching
author_sort Wu, Cheng-Mu
collection PubMed
description Stenotrophomonas maltophilia is a motile, opportunistic pathogen. The flagellum, which is involved in swimming, swarming, adhesion, and biofilm formation, is considered a virulence factor for motile pathogens. Three flagellin genes, fliC1, fliC2, and fliC3, were identified from the sequenced S. maltophilia genome. FliC1, fliC2, and fliC3 formed an operon, and their encoding proteins shared 67–82% identity. Members of the fliC1C2C3 operon were deleted individually or in combination to generate single mutants, double mutants, and a triple mutant. The contributions of the three flagellins to swimming, swarming, flagellum morphology, adhesion, and biofilm formation were assessed. The single mutants generally had a compromise in swimming and no significant defects in swarming, adhesion on biotic surfaces, and biofilm formation on abiotic surfaces. The double mutants displayed obvious defects in swimming and adhesion on abiotic and biotic surfaces. The flagellin-null mutant lost swimming ability and was compromised in adhesion and biofilm formation. All tested mutants demonstrated substantial but different flagellar morphologies, supporting that flagellin composition affects filament morphology. Bacterial swimming motility was significantly compromised under an oxidative stress condition, irrespective of flagellin composition. Collectively, the utilization of these three flagellins for filament assembly equips S. maltophilia with flagella adapted to provide better ability in swimming, adhesion, and biofilm formation for its pathogenesis.
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spelling pubmed-89984492022-04-12 Molecular Characterization of Three Tandemly Located Flagellin Genes of Stenotrophomonas maltophilia Wu, Cheng-Mu Huang, Hsin-Hui Li, Li-Hua Lin, Yi-Tsung Yang, Tsuey-Ching Int J Mol Sci Article Stenotrophomonas maltophilia is a motile, opportunistic pathogen. The flagellum, which is involved in swimming, swarming, adhesion, and biofilm formation, is considered a virulence factor for motile pathogens. Three flagellin genes, fliC1, fliC2, and fliC3, were identified from the sequenced S. maltophilia genome. FliC1, fliC2, and fliC3 formed an operon, and their encoding proteins shared 67–82% identity. Members of the fliC1C2C3 operon were deleted individually or in combination to generate single mutants, double mutants, and a triple mutant. The contributions of the three flagellins to swimming, swarming, flagellum morphology, adhesion, and biofilm formation were assessed. The single mutants generally had a compromise in swimming and no significant defects in swarming, adhesion on biotic surfaces, and biofilm formation on abiotic surfaces. The double mutants displayed obvious defects in swimming and adhesion on abiotic and biotic surfaces. The flagellin-null mutant lost swimming ability and was compromised in adhesion and biofilm formation. All tested mutants demonstrated substantial but different flagellar morphologies, supporting that flagellin composition affects filament morphology. Bacterial swimming motility was significantly compromised under an oxidative stress condition, irrespective of flagellin composition. Collectively, the utilization of these three flagellins for filament assembly equips S. maltophilia with flagella adapted to provide better ability in swimming, adhesion, and biofilm formation for its pathogenesis. MDPI 2022-03-31 /pmc/articles/PMC8998449/ /pubmed/35409223 http://dx.doi.org/10.3390/ijms23073863 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wu, Cheng-Mu
Huang, Hsin-Hui
Li, Li-Hua
Lin, Yi-Tsung
Yang, Tsuey-Ching
Molecular Characterization of Three Tandemly Located Flagellin Genes of Stenotrophomonas maltophilia
title Molecular Characterization of Three Tandemly Located Flagellin Genes of Stenotrophomonas maltophilia
title_full Molecular Characterization of Three Tandemly Located Flagellin Genes of Stenotrophomonas maltophilia
title_fullStr Molecular Characterization of Three Tandemly Located Flagellin Genes of Stenotrophomonas maltophilia
title_full_unstemmed Molecular Characterization of Three Tandemly Located Flagellin Genes of Stenotrophomonas maltophilia
title_short Molecular Characterization of Three Tandemly Located Flagellin Genes of Stenotrophomonas maltophilia
title_sort molecular characterization of three tandemly located flagellin genes of stenotrophomonas maltophilia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8998449/
https://www.ncbi.nlm.nih.gov/pubmed/35409223
http://dx.doi.org/10.3390/ijms23073863
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