Campos Cristina Belmar, Aepfelbacher Martin, Hentschke Moritz
Institute of Medical Microbiology, Virology and Hygiene, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
MVZ Labor Dr. Fenner und Kollegen, Bergstrasse 14, 20095 Hamburg.
New Microbiol. 2017 Apr;40(2):135-138. Epub 2017 Apr 3.
Mutations in ramR, a negative regulator of ramA which stimulates transcription of acrA/-B encoding the multidrug efflux pump AcrAB-TolC, were recently shown to result in reduced susceptibility to tigecycline in Klebsiella pneumoniae. We analysed six non-duplicate K. pneumoniae isolates with elevated MICs to tigecycline. All isolates showed transcriptional up-regulation of ramA and acrB as demonstrated by Northern blot and quantitative real-time PCR. Sequencing of the ramR gene revealed deletions in five of the isolates and a premature stop codon in one isolate. Transformation of the wild-type ramR gene but not of any of the detected mutant ramR genes into a ramR-mutant K. pneumoniae strain restored tigecycline susceptibility and repressed ramA and acrB transcription to wild type levels. Thus, our study confirms the role of inactivating mutations in the ramR gene in tigecycline resistance.
RamR是RamA的负调控因子,RamA可刺激编码多药外排泵AcrAB-TolC的acrA/-B的转录,最近研究表明,ramR突变会导致肺炎克雷伯菌对替加环素的敏感性降低。我们分析了6株对替加环素MIC升高的非重复肺炎克雷伯菌分离株。通过Northern印迹和定量实时PCR证明,所有分离株均显示ramA和acrB转录上调。ramR基因测序显示,其中5株分离株存在缺失,1株分离株存在提前终止密码子。将野生型ramR基因而非任何检测到的突变ramR基因转化到ramR突变的肺炎克雷伯菌菌株中,可恢复替加环素敏感性,并将ramA和acrB转录抑制到野生型水平。因此,我们的研究证实了ramR基因失活突变在替加环素耐药中的作用。