National Research Laboratory of Molecular Microbiology and Toxicology, Department of Agricultural Biotechnology, Seoul National University, Seoul, Republic of Korea.
Center for Food and Bioconvergence, Seoul National University, Seoul, Republic of Korea.
J Antimicrob Chemother. 2022 Aug 25;77(9):2419-2428. doi: 10.1093/jac/dkac223.
Outer membrane porins (OMPs) are a major route for the entry of small hydrophilic antibiotics. Thus, compositional modulation of OMPs is often accompanied by multidrug resistance in a human pathogen Salmonella enterica serovar Enteritidis.
The role of EnvZ/OmpR two-component system in antibiotic resistance has not been established except that it regulates the expression of two OMPs, OmpC and OmpF. Here, we have gained mechanistic insight into EnvZ/OmpR-mediated antibiotic resistance in S. Enteritidis.
The envZP248L and envZH243A strains, mimicking the S. Enteritidis strains with active and inactive states of EnvZ/OmpR, were used in this study. Antibiotic resistance was determined by the broth microdilution method and the spot plating assay. Transcriptomes of the S. Enteritidis strains were analysed by RNA-seq. Western blot, quantitative reverse transcription-PCR, electrophoretic mobility shift assays and β-galactosidase activity assays were performed.
The active state of EnvZ/OmpR induced a differential expression of multiple OMP genes including SEN1522, SEN2875, ompD and ompW, enhancing resistance to β-lactams in S. Enteritidis. OmpR directly activated SEN1522 and SEN2875 but repressed ompD and ompW. Interestingly, an increased cellular level of OmpR determined the expression of the four OMP genes, and phosphorylation of OmpR was even not necessary for the repression of ompD and ompW. EnvZ/OmpR increased its own expression in response to β-lactams, decreasing outer membrane permeability and providing S. Enteritidis with benefits for survival upon exposure to the antibiotics.
EnvZ/OmpR remodels OMP composition in response to β-lactams and thereby enhances antibiotic resistance in S. Enteritidis.
外膜孔蛋白(OMPs)是小分子亲水性抗生素进入的主要途径。因此,在人类病原体肠炎沙门氏菌血清型肠炎亚种中,OMPs 的组成调节通常伴随着多药耐药性。
除了调节两种 OMPs(OmpC 和 OmpF)的表达外,EnvZ/OmpR 二组分系统在抗生素耐药性中的作用尚未确定。在这里,我们深入了解了肠炎沙门氏菌中 EnvZ/OmpR 介导的抗生素耐药性的机制。
本研究使用了模拟肠炎沙门氏菌 EnvZ/OmpR 处于激活和失活状态的 envZP248L 和 envZH243A 菌株。通过肉汤微量稀释法和点平板法测定抗生素耐药性。通过 RNA-seq 分析肠炎沙门氏菌菌株的转录组。进行 Western blot、定量逆转录-PCR、电泳迁移率变动分析和β-半乳糖苷酶活性测定。
EnvZ/OmpR 的激活状态诱导了包括 SEN1522、SEN2875、ompD 和 ompW 在内的多种 OMP 基因的差异表达,增强了肠炎沙门氏菌对β-内酰胺类抗生素的耐药性。OmpR 直接激活 SEN1522 和 SEN2875,但抑制 ompD 和 ompW。有趣的是,OmpR 细胞内水平的增加决定了这四个 OMP 基因的表达,而 OmpR 的磷酸化甚至对于 ompD 和 ompW 的抑制也不是必需的。EnvZ/OmpR 对β-内酰胺类抗生素的反应增加了自身的表达,降低了外膜通透性,使肠炎沙门氏菌在暴露于抗生素时获得了生存优势。
EnvZ/OmpR 响应β-内酰胺类抗生素重塑 OMP 组成,从而增强了肠炎沙门氏菌的抗生素耐药性。