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雷氏弧菌 RaeE-RaeF-RopN 系统的特性研究,一种假定的 RND 外排泵系统。

Characterization of RaeE-RaeF-RopN, a putative RND efflux pump system in Riemerella anatipestifer.

机构信息

State Key Laboratory of Veterinary Etiological Biology, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, No. 1 Xujiaping, Yanchangbao, Lanzhou 730046, China.

State Key Laboratory of Veterinary Etiological Biology, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, No. 1 Xujiaping, Yanchangbao, Lanzhou 730046, China.

出版信息

Vet Microbiol. 2020 Dec;251:108852. doi: 10.1016/j.vetmic.2020.108852. Epub 2020 Sep 19.

Abstract

Resistance-nodulation-division (RND) efflux systems are ubiquitous in Gram-negative bacteria and play a predominant role in antimicrobial resistance and other diverse phenotypes, but the knowledges of RND efflux systems are poorly understood so far in Riemerella anatipestifer. According to the sequence annotation, RIA_1117-RIA_1118-RIA_1119 operon in RA-GD strain encodes a putative tripartite RND efflux system. RIA_1117, RIA_1118 and RIA_1119 genes encode an outer member protein (OMP), an inner membrane pump protein (pump transporter), and a periplasmic membrane fusion protein (MFP), respectively. Furthermore, RIA_1119 protein is annotated as a MexE component. In this work, the biological functions of RIA_1117-RIA_1118-RIA_1119 proteins were studied. The antibiotic susceptibility testing showed that the inactivation of RIA_1117, RIA_1118 and RIA_1119 genes all raised susceptibility to amikacin, streptomycin and SDS. By induction with the above antimicrobial agents, the transcription levels of RIA_1117 and RIA_1118 genes were up-regulated significantly using qRT-PCR detection, but no significance difference was observed for the transcription level of RIA_1119 gene. CCCP inhibitor assay confirmed that RIA_1117, RIA_1118 and RIA_1119 proteins mediated amikacin, streptomycin and SDS resistance depending on proton motive force (PMF). Spot assay and streptomycin accumulation assay confirmed that RIA_1117, RIA_1118 and RIA_1119 proteins contributed to export streptomycin, and CCCP increased the accumulation of streptomycin. Furthermore, RIA_1117, RIA_1118 and RIA_1119 proteins also were involved in the fitness and virulence of RA-GD strain. These results showed that RIA_1117-RIA_1118-RIA_1119 operon encoded a RND efflux system, which has the substrate specificity for streptomycin, amikacin and SDS and contributed to the growth and virulence of RA-GD. RIA_1117-RIA_1118-RIA_1119 was designated RaeE-RaeF-RopN efflux system. Based on the above results and structural analysis, RIA_1117, RIA_1118 and RIA_1119 proteins corresponded to RopN (OMP), RaeF (pump transporter) and RaeE (MFP), respectively.

摘要

耐药-结节-分裂(RND)外排系统在革兰氏阴性菌中普遍存在,在抗菌药物耐药性和其他多种表型中起着主要作用,但到目前为止,在鸭疫里默氏杆菌中对 RND 外排系统的了解还很有限。根据序列注释,RA-GD 株的 RIA_1117-RIA_1118-RIA_1119 操纵子编码一个假定的三联 RND 外排系统。RIA_1117、RIA_1118 和 RIA_1119 基因分别编码一个外膜蛋白(OMP)、一个内膜泵蛋白(泵转运蛋白)和一个周质膜融合蛋白(MFP)。此外,RIA_1119 蛋白被注释为 MexE 成分。在这项工作中,研究了 RIA_1117-RIA_1118-RIA_1119 蛋白的生物学功能。抗生素敏感性测试表明,RIA_1117、RIA_1118 和 RIA_1119 基因的失活均提高了对阿米卡星、链霉素和 SDS 的敏感性。通过用上述抗菌剂诱导,使用 qRT-PCR 检测发现 RIA_1117 和 RIA_1118 基因的转录水平显著上调,但 RIA_1119 基因的转录水平没有显著差异。CCCP 抑制剂测定证实,RIA_1117、RIA_1118 和 RIA_1119 蛋白通过质子动力势(PMF)介导阿米卡星、链霉素和 SDS 耐药。点样试验和链霉素积累试验证实,RIA_1117、RIA_1118 和 RIA_1119 蛋白有助于链霉素的外排,CCCP 增加了链霉素的积累。此外,RIA_1117、RIA_1118 和 RIA_1119 蛋白还参与了 RA-GD 株的适应性和毒力。这些结果表明,RIA_1117-RIA_1118-RIA_1119 操纵子编码一个 RND 外排系统,该系统对链霉素、阿米卡星和 SDS 具有底物特异性,并有助于 RA-GD 的生长和毒力。RIA_1117-RIA_1118-RIA_1119 被指定为 RaeE-RaeF-RopN 外排系统。基于上述结果和结构分析,RIA_1117、RIA_1118 和 RIA_1119 蛋白分别对应于 RopN(OMP)、RaeF(泵转运蛋白)和 RaeE(MFP)。

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