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Rho factor mediates flagellum and toxin phase variation and impacts virulence in Clostridioides difficile
The intestinal pathogen Clostridioides difficile exhibits heterogeneity in motility and toxin production. This phenotypic heterogeneity is achieved through phase variation by site-specific recombination via the DNA recombinase RecV, which reversibly inverts the “flagellar switch” upstream of the flg...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7446863/ https://www.ncbi.nlm.nih.gov/pubmed/32785266 http://dx.doi.org/10.1371/journal.ppat.1008708 |
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author | Trzilova, Dominika Anjuwon-Foster, Brandon R. Torres Rivera, Dariana Tamayo, Rita |
author_facet | Trzilova, Dominika Anjuwon-Foster, Brandon R. Torres Rivera, Dariana Tamayo, Rita |
author_sort | Trzilova, Dominika |
collection | PubMed |
description | The intestinal pathogen Clostridioides difficile exhibits heterogeneity in motility and toxin production. This phenotypic heterogeneity is achieved through phase variation by site-specific recombination via the DNA recombinase RecV, which reversibly inverts the “flagellar switch” upstream of the flgB operon. A recV mutation prevents flagellar switch inversion and results in phenotypically locked strains. The orientation of the flagellar switch influences expression of the flgB operon post-transcription initiation, but the specific molecular mechanism is unknown. Here, we report the isolation and characterization of spontaneous suppressor mutants in the non-motile, non-toxigenic recV flg OFF background that regained motility and toxin production. The restored phenotypes corresponded with increased expression of flagellum and toxin genes. The motile suppressor mutants contained single-nucleotide polymorphisms (SNPs) in rho, which encodes the bacterial transcription terminator Rho factor. Analyses using transcriptional reporters indicate that Rho contributes to heterogeneity in flagellar gene expression by preferentially terminating transcription of flg OFF mRNA within the 5’ leader sequence. Additionally, Rho is important for initial colonization of the intestine in a mouse model of infection, which may in part be due to the sporulation and growth defects observed in the rho mutants. Together these data implicate Rho factor as a regulator of gene expression affecting phase variation of important virulence factors of C. difficile. |
format | Online Article Text |
id | pubmed-7446863 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-74468632020-08-26 Rho factor mediates flagellum and toxin phase variation and impacts virulence in Clostridioides difficile Trzilova, Dominika Anjuwon-Foster, Brandon R. Torres Rivera, Dariana Tamayo, Rita PLoS Pathog Research Article The intestinal pathogen Clostridioides difficile exhibits heterogeneity in motility and toxin production. This phenotypic heterogeneity is achieved through phase variation by site-specific recombination via the DNA recombinase RecV, which reversibly inverts the “flagellar switch” upstream of the flgB operon. A recV mutation prevents flagellar switch inversion and results in phenotypically locked strains. The orientation of the flagellar switch influences expression of the flgB operon post-transcription initiation, but the specific molecular mechanism is unknown. Here, we report the isolation and characterization of spontaneous suppressor mutants in the non-motile, non-toxigenic recV flg OFF background that regained motility and toxin production. The restored phenotypes corresponded with increased expression of flagellum and toxin genes. The motile suppressor mutants contained single-nucleotide polymorphisms (SNPs) in rho, which encodes the bacterial transcription terminator Rho factor. Analyses using transcriptional reporters indicate that Rho contributes to heterogeneity in flagellar gene expression by preferentially terminating transcription of flg OFF mRNA within the 5’ leader sequence. Additionally, Rho is important for initial colonization of the intestine in a mouse model of infection, which may in part be due to the sporulation and growth defects observed in the rho mutants. Together these data implicate Rho factor as a regulator of gene expression affecting phase variation of important virulence factors of C. difficile. Public Library of Science 2020-08-12 /pmc/articles/PMC7446863/ /pubmed/32785266 http://dx.doi.org/10.1371/journal.ppat.1008708 Text en © 2020 Trzilova et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Trzilova, Dominika Anjuwon-Foster, Brandon R. Torres Rivera, Dariana Tamayo, Rita Rho factor mediates flagellum and toxin phase variation and impacts virulence in Clostridioides difficile |
title | Rho factor mediates flagellum and toxin phase variation and impacts virulence in Clostridioides difficile |
title_full | Rho factor mediates flagellum and toxin phase variation and impacts virulence in Clostridioides difficile |
title_fullStr | Rho factor mediates flagellum and toxin phase variation and impacts virulence in Clostridioides difficile |
title_full_unstemmed | Rho factor mediates flagellum and toxin phase variation and impacts virulence in Clostridioides difficile |
title_short | Rho factor mediates flagellum and toxin phase variation and impacts virulence in Clostridioides difficile |
title_sort | rho factor mediates flagellum and toxin phase variation and impacts virulence in clostridioides difficile |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7446863/ https://www.ncbi.nlm.nih.gov/pubmed/32785266 http://dx.doi.org/10.1371/journal.ppat.1008708 |
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