4.6 Article

The MqsR/MqsA toxin/antitoxin system protects Escherichia coli during bile acid stress

Journal

ENVIRONMENTAL MICROBIOLOGY
Volume 17, Issue 9, Pages 3168-3181

Publisher

WILEY
DOI: 10.1111/1462-2920.12749

Keywords

-

Categories

Funding

  1. ARO [W911NF-14-1-0279]
  2. NSF-CAREER award [MCB0952550]
  3. Direct For Biological Sciences
  4. Div Of Molecular and Cellular Bioscience [0952550] Funding Source: National Science Foundation

Ask authors/readers for more resources

Toxin/antitoxin (TA) systems are ubiquitous within bacterial genomes, and the mechanisms of many TA systems are well characterized. As such, several roles for TA systems have been proposed, such as phage inhibition, gene regulation and persister cell formation. However, the significance of these roles is nebulous due to the subtle influence from individual TA systems. For example, a single TA system has only a minor contribution to persister cell formation. Hence, there is a lack of defining physiological roles for individual TA systems. In this study, phenotype assays were used to determine that the MqsR/MqsA type II TA system of Escherichia coli is important for cell growth and tolerance during stress from the bile salt deoxycholate. Using transcriptomics and purified MqsR, we determined that endoribonuclease toxin MqsR degrades YgiS mRNA, which encodes a periplasmic protein that promotes deoxycholate uptake and reduces tolerance to deoxycholate exposure. The importance of reducing YgiS mRNA by MqsR is evidenced by improved growth, reduced cell death and reduced membrane damage when cells without ygiS are stressed with deoxycholate. Therefore, we propose that MqsR/MqsA is physiologically important for E.coli to thrive in the gallbladder and upper intestinal tract, where high bile concentrations are prominent.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available