a-fluorescence-based-method-to-study-bacterial-gene-regulation

A Fluorescence-based Method to Study Bacterial Gene Regulation in Infected Tissues

Bacterial virulence genes are often regulated at the transcriptional level by multiple factors that respond to different environmental signals. Some ...

Georgetown University

 subverts innate defenses during infection in part by killing host immune cells to exacerbate disease. This human pathogen intercepts host cues and activates a transcriptional response via the  exoprotein expression (SaeR/SaeS [SaeR/S]) two-component system to secrete virulence factors critical for pathogenesis. We recently showed that the transcriptional repressor CodY adjusts nuclease () gene expression via SaeR/S, but the mechanism remained unknown. Here, we identified two CodY binding motifs upstream of the  P1 promoter, which suggested direct regulation by this global regulator. We show that CodY shares a binding site with the positive activator SaeR and that alleviating direct CodY repression at this site is sufficient to abrogate stochastic expression, suggesting that CodY represses  expression by blocking SaeR binding. Epistasis experiments support a model that CodY also controls  indirectly through Agr and Rot-mediated repression of the  P1 promoter. We also demonstrate that CodY repression of  restrains production of secreted cytotoxins that kill human neutrophils. We conclude that CodY plays a previously unrecognized role in controlling virulence gene expression via SaeR/S and suggest a mechanism by which CodY acts as a master regulator of pathogenesis by tying nutrient availability to virulence gene expression. Bacterial mechanisms that mediate the switch from a commensal to pathogenic lifestyle are among the biggest unanswered questions in infectious disease research. Since the expression of most virulence genes is often correlated with nutrient depletion, this implies that virulence is a response to the lack of nourishment in host tissues and that pathogens like  produce virulence factors in order to gain access to nutrients in the host. Here, we show that specific nutrient depletion signals appear to be funneled to the SaeR/S system through the global regulator CodY. Our findings reveal a strategy by which  delays the production of immune evasion and immune-cell-killing proteins until key nutrients are depleted.

Kevin D. Mlynek

Department of Biology

Georgetown University

A Fluorescence-based Method to Study Bacterial Gene Regulation in Infected Tissues

Kevin D. Mlynek

.css-o250i3{font-size:18px;font-family:Open Sans,sans-serif;line-height:21.6px;}Department of Biology

Georgetown University

A Fluorescence-based Method to Study Bacterial Gene Regulation in Infected Tissues

Department of Biology