Programmed cell death in bacteria and implications for antibiotic therapy

被引:68
作者
Tanouchi, Yu [1 ]
Lee, Anna Jisu [1 ]
Meredith, Hannah [1 ]
You, Lingchong [1 ,2 ,3 ]
机构
[1] Duke Univ, Dept Biomed Engn, Durham, NC 27708 USA
[2] Duke Univ, Inst Genome Sci & Policy, Durham, NC 27708 USA
[3] Duke Univ, Ctr Syst Biol, Durham, NC 27708 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
programmed cell death; bacterial cooperation; synthetic biology; antibiotic therapy; ESCHERICHIA-COLI; SOCIAL EVOLUTION; SHIGA TOXIN; COOPERATION; VIRULENCE; TARGETS;
D O I
10.1016/j.tim.2013.04.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
It is now well appreciated that programmed cell death (PCD) plays critical roles in the life cycle of diverse bacterial species. It is an apparently paradoxical behavior as it does not benefit the cells undergoing PCD. However, growing evidence suggests that PCD can be 'altruistic': the dead cells may directly or indirectly benefit survivors through generation of public goods. This property provides a potential explanation on how PCD can evolve as an extreme form of cooperation, although many questions remain to be addressed. From another perspective, as PCD plays a critical role in bacterial pathogenesis, it has been proposed as a potential target for new antibacterial therapy. To this end, understanding the population and evolutionary dynamics resulting from PCD and public goods production may be a key to the success of designing effective antibiotic treatment.
引用
收藏
页码:265 / 270
页数:6
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