流出
质粒
多重耐药
抗药性
微生物学
化学
生物
遗传学
基因
作者
Sophie Nolivos,Julien Cayron,Annick Berne-Dedieu,Adeline Page,Frédéric Delolme,Christian Lesterlin
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2019-05-23
卷期号:364 (6442): 778-782
被引量:213
标识
DOI:10.1126/science.aav6390
摘要
A race against time Clinically relevant antimicrobial resistance is largely spread via plasmids that disperse among bacteria during conjugation. How quickly can a resistance gene be expressed after transfer? In susceptible bacterial cells, tetracycline should inhibit protein synthesis, including from the plasmid-transferred resistance gene tetA . Unexpectedly, Nolivos et al. found that TetA can be expressed despite the presence of tetracycline (see the Perspective by Povolo and Ackermann). Immediately after plasmid transfer into a cell, TetA synthesis starts because its repressor is slow to be expressed. In addition, the ubiquitous xenobiotic efflux pump AcrAB-TolC buys time for TetA translation by keeping tetracycline concentration below toxic levels. Science , this issue p. 778 ; see also p. 737
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