Generation of reactive oxygen species by lethal attacks from competing microbes

被引:130
作者
Dong, Tao G. [1 ,2 ]
Dong, Shiqi [1 ,2 ]
Catalano, Christy [1 ,2 ]
Moore, Richard [1 ,2 ]
Liang, Xiaoye [1 ,2 ]
Mekalanos, John J. [3 ]
机构
[1] Univ Calgary, Snyder Inst Chron Dis, Calgary, AB T2N 4Z6, Canada
[2] Univ Calgary, Dept Ecosyst & Publ Hlth, Calgary, AB T2N 4Z6, Canada
[3] Harvard Univ, Sch Med, Dept Microbiol & Immunobiol, Boston, MA 02115 USA
关键词
T6SS; reactive oxygen species; interspecies competition; antibiotics; phage; VI SECRETION SYSTEM; MEDIATED CELL-DEATH; ESCHERICHIA-COLI; VIBRIO-CHOLERAE; BACTERICIDAL ANTIBIOTICS; HYDROGEN-PEROXIDE; OXIDATIVE STRESS; PROTEIN; DAMAGE; IDENTIFICATION;
D O I
10.1073/pnas.1425007112
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Whether antibiotics induce the production of reactive oxygen species (ROS) that contribute to cell death is an important yet controversial topic. Here, we report that lethal attacks from bacterial and viral species also result in ROS production in target cells. Using soxS as an ROS reporter, we found soxS was highly induced in Escherichia coli exposed to various forms of attacks mediated by the type VI secretion system(T6SS), P1vir phage, and polymyxin B. Using a fluorescence ROS probe, we found enhanced ROS levels correlate with induced soxS in E. coli expressing a toxic T6SS antibacterial effector and in E. coli treated with P1vir phage or polymyxin B. We conclude that both contact-dependent and contact-independent interactions with aggressive competing bacterial species and viruses can induce production of ROS in E. coli target cells.
引用
收藏
页码:2181 / 2186
页数:6
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