Instituto Gulbenkian de Ciência, Oeiras, Portugal.
Instituto Gulbenkian de Ciência, Oeiras, Portugal.
Trends Microbiol. 2018 Aug;26(8):677-691. doi: 10.1016/j.tim.2018.01.005. Epub 2018 Feb 10.
Antibiotics target essential cellular functions but bacteria can become resistant by acquiring either exogenous resistance genes or chromosomal mutations. Resistance mutations typically occur in genes encoding essential functions; these mutations are therefore generally detrimental in the absence of drugs. However, bacteria can reduce this handicap by acquiring additional mutations, known as compensatory mutations. Genetic interactions (epistasis) either with the background or between resistances (in multiresistant bacteria) dramatically affect the fitness cost of antibiotic resistance and its compensation, therefore shaping dissemination of antibiotic resistance mutations. This Review summarizes current knowledge on the evolutionary mechanisms influencing maintenance of resistance mediated by chromosomal mutations, focusing on their fitness cost, compensatory evolution, epistasis, and the effect of the environment on these processes.
抗生素针对的是细胞的基本功能,但细菌可以通过获得外源性抗性基因或染色体突变而产生抗性。抗性突变通常发生在编码基本功能的基因中;因此,在没有药物的情况下,这些突变通常是有害的。然而,细菌可以通过获得额外的突变来减少这种劣势,这些突变被称为补偿性突变。遗传相互作用(上位性)无论是与背景还是与抗性之间(在多抗性细菌中),都会极大地影响抗生素抗性的适应性成本及其补偿,从而影响抗生素抗性突变的传播。这篇综述总结了目前关于影响由染色体突变介导的抗性维持的进化机制的知识,重点关注其适应性成本、补偿进化、上位性以及环境对这些过程的影响。