4.4 Article

RyhB, an iron-responsive small RNA molecule, regulates Shigella dysenteriae virulence

Journal

INFECTION AND IMMUNITY
Volume 75, Issue 7, Pages 3470-3477

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/IAI.00112-07

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Funding

  1. NIAID NIH HHS [R37 AI016935, AI 16935, R01 AI016935] Funding Source: Medline
  2. NIGMS NIH HHS [F32 GM069312] Funding Source: Medline

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Regulation of bacterial gene expression by small RNA (sRNA) molecules is an increasingly recognized phenomenon but one that is not yet fully understood. We show that the sRNA RyhB suppresses several virulence-associated phenotypes of Shigella dysenteriae, a causative agent of bacillary dysentery in humans. The virulence genes repressed by S. dysenteriae RyhB include those encoding the type III secretion apparatus, its secreted effectors, and specific chaperones. Suppression of Shigella virulence occurs via RyhB-dependent repression of the transcriptional activator VirB, leading to reduced expression of genes within the VirB regulon. Efficient repression of virB is mediated by a single-stranded region of RyhB that is distinct from the region required for repression of Shigella sodB. Regulation of virB by RyhB implicates iron as an environmental factor contributing to the complex regulation of Shigella virulence determinants.

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