TY - JOUR
T1 - YihE Kinase Is a Central Regulator of Programmed Cell Death in Bacteria
AU - Dorsey-Oresto, Angella
AU - Lu, Tao
AU - Mosel, Michael
AU - Wang, Xiuhong
AU - Salz, Tal
AU - Drlica, Karl
AU - Zhao, Xilin
N1 - Funding Information:
We thank Babak Baseri, Liping Li, Yulin Qu, and Yuzhi Hong for technical assistance, and Marila Gennaro, Ming Lu, David Perlin, Richard Pine, Issar Smith, and Sanjay Tyagi for critical comments on the manuscript. This work was supported by grants from the National Institutes of Health (1-DP2-OD007423, 1-R01-AI 073491, and 1-R21-AI 068014-01A2) and the National Natural Science Foundation of China (30860012 and 30973596).
PY - 2013
Y1 - 2013
N2 - Stress-mediated programmed cell death (PCD) in bacteria has recently attracted attention, largely because it raises novel possibilities for controlling pathogens. How PCD in bacteria is regulated to avoid population extinction due to transient, moderate stress remains a central question. Here, we report that the YihE protein kinase is a key regulator that protects Escherichia coli from antimicrobial and environmental stressors by antagonizing the MazEF toxin-antitoxin module. YihE was linked to a reactive oxygen species (ROS) cascade, and a deficiency of yihE stimulated stress-induced PCD even after stress dissipated. YihE was partially regulated by the Cpx envelope stress-response system, which, along with MazF toxin and superoxide, has both protective and destructive roles that help bacteria make a live-or-die decision in response to stress. YihE probably acts early in the stress response to limit self-sustaining ROS production and PCD. Inhibition of YihE may provide a way of enhancing antimicrobial lethality and attenuating virulence.
AB - Stress-mediated programmed cell death (PCD) in bacteria has recently attracted attention, largely because it raises novel possibilities for controlling pathogens. How PCD in bacteria is regulated to avoid population extinction due to transient, moderate stress remains a central question. Here, we report that the YihE protein kinase is a key regulator that protects Escherichia coli from antimicrobial and environmental stressors by antagonizing the MazEF toxin-antitoxin module. YihE was linked to a reactive oxygen species (ROS) cascade, and a deficiency of yihE stimulated stress-induced PCD even after stress dissipated. YihE was partially regulated by the Cpx envelope stress-response system, which, along with MazF toxin and superoxide, has both protective and destructive roles that help bacteria make a live-or-die decision in response to stress. YihE probably acts early in the stress response to limit self-sustaining ROS production and PCD. Inhibition of YihE may provide a way of enhancing antimicrobial lethality and attenuating virulence.
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U2 - 10.1016/j.celrep.2013.01.026
DO - 10.1016/j.celrep.2013.01.026
M3 - Article
C2 - 23416055
AN - SCOPUS:84874281193
SN - 2211-1247
VL - 3
SP - 528
EP - 537
JO - Cell Reports
JF - Cell Reports
IS - 2
ER -