Uppsala University, Department of Medical Biochemistry and Microbiology, Uppsala, Sweden.
PLoS Biol. 2022 Sep 28;20(9):e3001808. doi: 10.1371/journal.pbio.3001808. eCollection 2022 Sep.
In a collection of Escherichia coli isolates, we discovered a new mechanism leading to frequent and high-level tigecycline resistance involving tandem gene amplifications of an efflux pump encoded by the tet(A) determinant. Some isolates, despite carrying a functional tet(A), could not evolve high-level tigecycline resistance by amplification due to the presence of a deletion in the TetR(A) repressor. This mutation impaired induction of tetA(A) (encoding the TetA(A) efflux pump) in presence of tetracyclines, with the strongest effect observed for tigecycline, subsequently preventing the development of tet(A) amplification-dependent high-level tigecycline resistance. We found that this mutated tet(A) determinant was common among tet(A)-carrying E. coli isolates and analysed possible explanations for this high frequency. First, while the mutated tet(A) was found in several ST-groups, we found evidence of clonal spread among ST131 isolates, which increases its frequency within E. coli databases. Second, evolution and competition experiments revealed that the mutation in tetR(A) could be positively selected over the wild-type allele at sub-inhibitory concentrations of tetracyclines. Our work demonstrates how low concentrations of tetracyclines, such as those found in contaminated environments, can enrich and select for a mutation that generates an evolutionary dead-end that precludes the evolution towards high-level, clinically relevant tigecycline resistance.
在一组大肠杆菌分离株中,我们发现了一种新的机制,导致频繁和高水平的替加环素耐药性,涉及到由 tet(A)决定簇编码的外排泵的串联基因扩增。一些分离株尽管携带功能性 tet(A),但由于 TetR(A)阻遏物的缺失,不能通过扩增来产生高水平的替加环素耐药性。这种突变削弱了 tetracyclines 存在时 tetA(A)(编码 TetA(A)外排泵)的诱导,替加环素的效果最强,随后阻止了 tet(A)扩增依赖性高水平替加环素耐药性的发展。我们发现这种突变的 tet(A)决定簇在携带 tet(A)的大肠杆菌分离株中很常见,并分析了这种高频率的可能解释。首先,虽然突变的 tet(A)存在于几个 ST 组中,但我们发现 ST131 分离株中存在克隆传播的证据,这增加了其在大肠杆菌数据库中的频率。其次,进化和竞争实验表明,tetR(A)中的突变可以在低于抑制浓度的四环素浓度下被选择为野生型等位基因。我们的工作表明,环境中存在的低浓度四环素(如受污染环境中的四环素)如何富集和选择产生一种进化死胡同的突变,从而阻止向高水平、临床相关的替加环素耐药性的进化。