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...
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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. |
doi_str_mv | 10.1371/journal.ppat.1008708 |
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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.</description><identifier>ISSN: 1553-7374</identifier><identifier>ISSN: 1553-7366</identifier><identifier>EISSN: 1553-7374</identifier><identifier>DOI: 10.1371/journal.ppat.1008708</identifier><identifier>PMID: 32785266</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>5' Untranslated Regions ; Animals ; Bacteria ; Bacterial Proteins - genetics ; Bacterial Proteins - metabolism ; Bacterial Toxins - genetics ; Bacterial Toxins - metabolism ; Biology and Life Sciences ; Clostridioides difficile - genetics ; Clostridioides difficile - metabolism ; Clostridioides difficile - pathogenicity ; Clostridium ; Clostridium Infections - microbiology ; Colonization ; Deoxyribonucleic acid ; DNA ; DNA recombinase ; Female ; Filaggrin Proteins ; Flagella ; Flagella - genetics ; Flagella - metabolism ; Gene expression ; Gene Expression Regulation, Bacterial ; Genetic aspects ; Heterogeneity ; Humans ; Immunology ; Intestine ; Male ; Medicine ; Medicine and Health Sciences ; Mice ; Mice, Inbred C57BL ; Motility ; Mutation ; Nosocomial infections ; Nucleotides ; Operon ; Phase variations ; Phenotypes ; Post-transcription ; Properties ; Recombinase ; Recombinases ; Recombination ; Rho Factor - genetics ; Rho Factor - metabolism ; Single-nucleotide polymorphism ; Sporulation ; Suppressor mutant ; Toxins ; Transcription factors ; Transcription termination factor RHO ; Virulence ; Virulence (Microbiology) ; Virulence factors</subject><ispartof>PLoS pathogens, 2020-08, Vol.16 (8), p.e1008708</ispartof><rights>COPYRIGHT 2020 Public Library of Science</rights><rights>2020 Trzilova et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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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.</description><subject>5' Untranslated Regions</subject><subject>Animals</subject><subject>Bacteria</subject><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - metabolism</subject><subject>Bacterial Toxins - genetics</subject><subject>Bacterial Toxins - metabolism</subject><subject>Biology and Life Sciences</subject><subject>Clostridioides difficile - genetics</subject><subject>Clostridioides difficile - metabolism</subject><subject>Clostridioides difficile - pathogenicity</subject><subject>Clostridium</subject><subject>Clostridium Infections - microbiology</subject><subject>Colonization</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA recombinase</subject><subject>Female</subject><subject>Filaggrin Proteins</subject><subject>Flagella</subject><subject>Flagella - genetics</subject><subject>Flagella - metabolism</subject><subject>Gene expression</subject><subject>Gene Expression Regulation, Bacterial</subject><subject>Genetic aspects</subject><subject>Heterogeneity</subject><subject>Humans</subject><subject>Immunology</subject><subject>Intestine</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine and Health Sciences</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Motility</subject><subject>Mutation</subject><subject>Nosocomial infections</subject><subject>Nucleotides</subject><subject>Operon</subject><subject>Phase variations</subject><subject>Phenotypes</subject><subject>Post-transcription</subject><subject>Properties</subject><subject>Recombinase</subject><subject>Recombinases</subject><subject>Recombination</subject><subject>Rho Factor - genetics</subject><subject>Rho Factor - metabolism</subject><subject>Single-nucleotide polymorphism</subject><subject>Sporulation</subject><subject>Suppressor mutant</subject><subject>Toxins</subject><subject>Transcription factors</subject><subject>Transcription termination factor RHO</subject><subject>Virulence</subject><subject>Virulence (Microbiology)</subject><subject>Virulence factors</subject><issn>1553-7374</issn><issn>1553-7366</issn><issn>1553-7374</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNqVkktv1DAUhSMEoqXwDxBEYgOLGfy2s6lUjXiMVIFUYG3dOPaMR0kc7KQq_x5PJ606qBuUhSP7O8f3Ht-ieI3RElOJP-7CFHtol8MA4xIjpCRST4pTzDldSCrZ0wf_J8WLlHYIMUyxeF6cUCIVJ0KcFv5qG0oHZgyx7GzjYbSpdC1sbNtOXQl9U47hxvflsIVky2uIGfGhvz3x3ZCVqbz2cWptb2yZwVUb0hh944NvslfjnfPGt_Zl8cxBm-yreT0rfn3-9HP1dXH5_ct6dXG5MFwKtWDgOK8cKOuQaaiTSrlG1Ax4U1NeEYwoohhILYmoLdQ1EFNhqiRwRirF6Vnx9uA75EL0nFLShDEqsKCYZmJ9IJoAOz1E30H8owN4fbsR4kZDHL1prSaEc2dEZZ1EzNqqBsEZlsBqTpHBNnudz7dNdc7P2H6M0B6ZHp_0fqs34VpLxoQS-2LezwYx_J5sGnXnk8npQ2_DtK-bMiQwliSj7_5BH-9upjaQG_C9C_leszfVF4Ky7EeRytTyESp_je28Cb11-cmOBR-OBJkZ7c24gSklvf5x9R_st2OWHVgTQ0rRuvvsMNL7Qb9rUu8HXc-DnmVvHuZ-L7qbbPoXyDr5wQ</recordid><startdate>20200812</startdate><enddate>20200812</enddate><creator>Trzilova, Dominika</creator><creator>Anjuwon-Foster, Brandon R</creator><creator>Torres Rivera, Dariana</creator><creator>Tamayo, Rita</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISN</scope><scope>ISR</scope><scope>3V.</scope><scope>7QL</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-3745-3316</orcidid><orcidid>https://orcid.org/0000-0003-3165-6443</orcidid></search><sort><creationdate>20200812</creationdate><title>Rho factor mediates flagellum and toxin phase variation and impacts virulence in Clostridioides difficile</title><author>Trzilova, Dominika ; Anjuwon-Foster, Brandon R ; Torres Rivera, Dariana ; Tamayo, Rita</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5768-4af559fa8ef0cd3f788fd6b4a5db3592103031a2b726beabba2c91387a5429853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>5' Untranslated Regions</topic><topic>Animals</topic><topic>Bacteria</topic><topic>Bacterial Proteins - genetics</topic><topic>Bacterial Proteins - metabolism</topic><topic>Bacterial Toxins - genetics</topic><topic>Bacterial Toxins - metabolism</topic><topic>Biology and Life Sciences</topic><topic>Clostridioides difficile - genetics</topic><topic>Clostridioides difficile - metabolism</topic><topic>Clostridioides difficile - pathogenicity</topic><topic>Clostridium</topic><topic>Clostridium Infections - microbiology</topic><topic>Colonization</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA recombinase</topic><topic>Female</topic><topic>Filaggrin Proteins</topic><topic>Flagella</topic><topic>Flagella - genetics</topic><topic>Flagella - metabolism</topic><topic>Gene expression</topic><topic>Gene Expression Regulation, Bacterial</topic><topic>Genetic aspects</topic><topic>Heterogeneity</topic><topic>Humans</topic><topic>Immunology</topic><topic>Intestine</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine and Health Sciences</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Motility</topic><topic>Mutation</topic><topic>Nosocomial infections</topic><topic>Nucleotides</topic><topic>Operon</topic><topic>Phase variations</topic><topic>Phenotypes</topic><topic>Post-transcription</topic><topic>Properties</topic><topic>Recombinase</topic><topic>Recombinases</topic><topic>Recombination</topic><topic>Rho Factor - genetics</topic><topic>Rho Factor - metabolism</topic><topic>Single-nucleotide polymorphism</topic><topic>Sporulation</topic><topic>Suppressor mutant</topic><topic>Toxins</topic><topic>Transcription factors</topic><topic>Transcription termination factor RHO</topic><topic>Virulence</topic><topic>Virulence (Microbiology)</topic><topic>Virulence factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Trzilova, Dominika</creatorcontrib><creatorcontrib>Anjuwon-Foster, Brandon R</creatorcontrib><creatorcontrib>Torres Rivera, Dariana</creatorcontrib><creatorcontrib>Tamayo, Rita</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Canada</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection (ProQuest)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PLoS pathogens</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Trzilova, Dominika</au><au>Anjuwon-Foster, Brandon R</au><au>Torres Rivera, Dariana</au><au>Tamayo, Rita</au><au>McClane, Bruce A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rho factor mediates flagellum and toxin phase variation and impacts virulence in Clostridioides difficile</atitle><jtitle>PLoS pathogens</jtitle><addtitle>PLoS Pathog</addtitle><date>2020-08-12</date><risdate>2020</risdate><volume>16</volume><issue>8</issue><spage>e1008708</spage><pages>e1008708-</pages><issn>1553-7374</issn><issn>1553-7366</issn><eissn>1553-7374</eissn><abstract>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.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>32785266</pmid><doi>10.1371/journal.ppat.1008708</doi><orcidid>https://orcid.org/0000-0002-3745-3316</orcidid><orcidid>https://orcid.org/0000-0003-3165-6443</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 5' Untranslated Regions Animals Bacteria Bacterial Proteins - genetics Bacterial Proteins - metabolism Bacterial Toxins - genetics Bacterial Toxins - metabolism Biology and Life Sciences Clostridioides difficile - genetics Clostridioides difficile - metabolism Clostridioides difficile - pathogenicity Clostridium Clostridium Infections - microbiology Colonization Deoxyribonucleic acid DNA DNA recombinase Female Filaggrin Proteins Flagella Flagella - genetics Flagella - metabolism Gene expression Gene Expression Regulation, Bacterial Genetic aspects Heterogeneity Humans Immunology Intestine Male Medicine Medicine and Health Sciences Mice Mice, Inbred C57BL Motility Mutation Nosocomial infections Nucleotides Operon Phase variations Phenotypes Post-transcription Properties Recombinase Recombinases Recombination Rho Factor - genetics Rho Factor - metabolism Single-nucleotide polymorphism Sporulation Suppressor mutant Toxins Transcription factors Transcription termination factor RHO Virulence Virulence (Microbiology) Virulence factors |
title | Rho factor mediates flagellum and toxin phase variation and impacts virulence in Clostridioides difficile |
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