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Efflux pump gene hefA of Helicobacter pylori plays an important role in multidrug resistance

机译:幽门螺杆菌外排泵基因hefA在多药耐药中起重要作用

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摘要

AIM: To determine whether efflux systems contribute to multidrug resistance of H pylori.METHODS: A chloramphenicol-induced multidrug resistance model of six susceptible H pylori strains (5 isolates and H pylori NCTC11637) was developed. Multidrug-resistant (MDR) strains were selected and the minimal inhibitory concentration (MIC) of erythromycin, metronidazole, penicillin G, tetracycline, and ciprofloxacin in multidrug resistant strains and their parent strains was determined by agar dilution tests. The level of mRNA expression of hefA was assessed by fluorescence real-time quantitative PCR. A H pylori LZ1026 knockout mutant (ΔH pylori LZ1026) for (putative) efflux protein was constructed by inserting the kanamycin resistance cassette from pEGFP-N2 into hefA, and its susceptibility profiles to 10 antibiotics were evaluated.RESULTS: The MIC of six multidrug-resistant strains (including 5 clinical isolates and H pylori NCTC11637) increased significantly (≥ 4-fold) compared with their parent strains. The expression level of hefA gene was significantly higher in the MDR strains than in their parent strains (P = 0.033). A H pylori LZ1026 mutant was successfully constructed and the ΔH pylori LZ1026 was more susceptible to four of the 10 antibiotics. All the 20 strains displayed transcripts for hefA that confirmed the in vitro expression of these genes.CONCLUSION: The efflux pump gene hefA plays an important role in multidrug resistance of H pylori.
机译:目的:确定外排系统是否有助于幽门螺杆菌的多重耐药性。方法:建立了氯霉素诱导的六种敏感幽门螺杆菌菌株(5个分离物和幽门螺杆菌NCTC11637)的多重耐药性模型。选择耐多药(MDR)菌株,并通过琼脂稀释试验确定多药抗性菌株及其亲本菌株中红霉素,甲硝唑,青霉素G,四环素和环丙沙星的最低抑菌浓度(MIC)。通过荧光实时定量PCR评估hefA的mRNA表达水平。通过将来自pEGFP-N2的卡那霉素抗性盒插入hefA中,构建AH幽门螺杆菌LZ1026敲除突变体(ΔH幽门螺杆菌LZ1026),并评估其对10种抗生素的敏感性。结果:六种耐多药的MIC菌株(包括5种临床分离株和幽门螺杆菌NCTC11637)与其亲本菌株相比显着增加(≥4倍)​​。 MDR菌株中hefA基因的表达水平明显高于其亲本菌株(P = 0.033)。成功构建了H幽门螺杆菌LZ1026突变体,而ΔH幽门螺杆菌LZ1026对10种抗生素中的四种更敏感。这20个菌株均显示出hefA的转录本,证实了这些基因的体外表达。结论:外排泵基因hefA在幽门螺杆菌的多药耐药中起重要作用。

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