PLoS Pathogens · 2020 · 39 citations · 92 references
Life SciencesMicrobiologyMolecular BiologyGene ExpressionMicrobial GeneticsMicrobial PathogenesisBacterial MotilityBacterial PathogenesisBacterial Virulence FactorsMicrobial Virulence FactorsPathogen Virulence FactorsToxin ProductionBacterial Toxin ProductionFlagellar Virulence FactorsFlagellar Virulence TraitsMotility MutantsPathogenesis Of Bacterial ToxinsRegulation Of Toxin ExpressionToxin Gene RegulationToxin Genes
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.
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Glucosylation of Rho proteins by Clostridium difficile toxin B
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