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The Chromosomal Toxin Gene yafQ Is a Determinant of Multidrug Tolerance for Escherichia coli Growing in a Biofilm

机译:染色体毒素基因yafQ是在生物膜中生长的大肠杆菌的多药耐受性的决定因素。

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摘要

Escherichia coli is refractory to elevated doses of antibiotics when it is growing in a biofilm, and this is potentially due to high numbers of multidrug-tolerant persister cells in the surface-adherent population. Previously, the chromosomal toxin-antitoxin loci hipBA and relBE have been linked to the frequency at which persister cells occur in E. coli populations. In the present study, we focused on the dinJ-yafQ-encoded toxin-antitoxin system and hypothesized that deletion of the toxin gene yafQ might influence cell survival in antibiotic-exposed biofilms. By using confocal laser scanning microscopy and viable cell counting, it was determined that a ΔyafQ mutant produced biofilms with a structure and a cell density equivalent to those of the parental strain. In-depth susceptibility testing identified that relative to wild-type E. coli, the ΔyafQ strain had up to a ∼2,400-fold decrease in cell survival after the biofilms were exposed to bactericidal concentrations of cefazolin or tobramycin. Corresponding to these data, controlled overexpression of yafQ from a high-copy-number plasmid resulted in up to a ∼10,000-fold increase in the number of biofilm cells surviving exposure to these bactericidal drugs. In contrast, neither the inactivation nor the overexpression of yafQ affected the tolerance of biofilms to doxycycline or rifampin (rifampicin). Furthermore, deletion of yafQ did not affect the tolerance of stationary-phase planktonic cells to any of the antibacterials tested. These results suggest that yafQ mediates the tolerance of E. coli biofilms to multiple but specific antibiotics; moreover, our data imply that this cellular pathway for persistence is likely different from that of multidrug-tolerant cells in stationary-phase planktonic cell cultures.
机译:当大肠杆菌在生物膜中生长时,对高剂量的抗生素难治,这可能是由于表面贴壁人群中大量的耐多药持久性细胞所致。以前,染色体毒素-抗毒素基因座hipBA和relBE与大肠杆菌群体中持久性细胞的出现频率有关。在本研究中,我们集中于dinJ-yafQ编码的毒素-抗毒素系统,并假设毒素基因yafQ的缺失可能影响暴露于抗生素的生物膜中的细胞存活。通过使用共聚焦激光扫描显微镜和活细胞计数,可以确定ΔyafQ突变体产生的生物膜具有与亲本菌株相同的结构和细胞密度。深入的敏感性测试表明,相对于野生型大肠杆菌,在生物膜暴露于头孢唑林或妥布霉素的杀菌浓度后,ΔyafQ菌株的细胞存活率降低了约2400倍。与这些数据相对应的是,从高拷贝数的质粒中控制的yafQ的过表达导致在暴露于这些杀菌药物后存活的生物膜细胞数量增加了约10,000倍。相反,yafQ的失活或过表达都不会影响生物膜对强力霉素或利福平(rifampicin)的耐受性。此外,删除yafQ不会影响固定相浮游细胞对任何测试的抗生素的耐受性。这些结果表明,yafQ介导了大肠杆菌生物膜对多种但特定的抗生素的耐受性。此外,我们的数据表明,这种持久性细胞途径可能与固定相浮游细胞培养物中的多药耐受细胞不同。

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