The evolution of contact-dependent inhibition in non-growing populations of Escherichia coli

被引:33
作者
Lemonnier, Marc [1 ,2 ,3 ]
Levin, Bruce R. [1 ]
Romeo, Tony [4 ]
Garner, Kim [1 ]
Baquero, Maria-Rosario [5 ]
Mercante, Jeff [4 ]
Lemichez, Emmanuel [3 ]
Baquero, Fernando [5 ]
Blazquez, Jesus [6 ]
机构
[1] Emory Univ, Dept Biol, Atlanta, GA 30322 USA
[2] CSIC, Ctr Invest Biol, Dept Mol Microbiol, E-28040 Madrid, Spain
[3] Fac Med, INSERM, U627, F-06107 Nice, France
[4] Emory Univ, Sch Med, Dept Microbiol & Immunol, Atlanta, GA 30322 USA
[5] Hosp Ramon & Cajal, Dept Microbiol, E-28034 Madrid, Spain
[6] CSIC, Ctr Nacl Biotecnol, Dept Biotecnol Microbiana, E-28049 Madrid, Spain
关键词
Escherichia coli; allelopathy; parallel evolution; glycogen; population biology; mathematical models;
D O I
10.1098/rspb.2007.1234
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In the course of liquid culture, serial passage experiments with Escherichia coli K-12 bearing a mutator gene deletion (Delta mutS) we observed the evolution of strains that appeared to kill or inhibit the growth of the bacteria from where they were derived, their ancestors. We demonstrate that this inhibition occurs after the cells stop growing and requires physical contact between the evolved and ancestral bacteria. Thereby, it is referred to as stationary phase contact-dependent inhibition (SCDI). The evolution of this antagonistic relationship is not anticipated from existing theory and experiments of competition in mass (liquid) culture. Nevertheless, it occurred in the same way (parallel evolution) in the eight independent serial transfer cultures, through different single base substitutions in a gene in the glycogen synthesis pathway, glgC. We demonstrate that the observed mutations in glgC, which codes for ADP-glucose pyrophosphorylase, are responsible for both the ability of the evolved bacteria to inhibit or kill their ancestors and their immunity to that inhibition or killing. We present evidence that without additional evolution, mutator genes, or known mutations in glgC, other strains of E. coli K-12 are also capable of SCDI or sensitive to this inhibition. We interpret this, in part, as support for the generality of SCDI and also as suggesting that the glgC mutations responsible for the SCDI, which evolved in our experiments, may suppress the action of one or more genes responsible for the sensitivity of E. coli to SCDI. Using numerical solutions to a mathematical model and in vitro experiments, we explore the population dynamics of SCDI and postulate the conditions responsible for its evolution in mass culture. We conclude with a brief discussion of the potential ecological significance of SCDI and its possible utility for the development of antimicrobial agents, which unlike existing antibiotics, can kill or inhibit the growth of bacteria that are not growing.
引用
收藏
页码:3 / 10
页数:8
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