氧化铜纳米颗粒与氯霉素对耐药铜绿假单胞菌泵外系统MexA基因表达的协同作用

Faten Alazavi, Farahnaz - Molavi, Maryam Tehranipoor
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引用次数: 0

摘要

背景。铜绿假单胞菌是医院感染的病原体。氯霉素是一种广谱、廉价、常用的抗生素。MexAB-OprM是一种分泌泵,引起这种细菌的先天抗性。本研究旨在评价纳米铜和氯霉素对MexA基因表达的影响。方法。在这项研究中,从伊朗马什哈德的11个实验室收集了49个样本。采用聚合酶链反应(PCR)法检测Me基因MexA的丰度,采用纸片扩散法进行药敏评价。为了计算最小抑制浓度(MIC)和最小杀菌浓度(MBC),铜纳米颗粒,以及两者的组合,进行了肉汤稀释法。采用微量稀释法和实时PCR技术分别测定氧化铜纳米颗粒和氯霉素的有效稀释度和MexA基因的表达。结果。确认了49株菌株的身份。所有菌株都含有MexA基因,并且对两种以上的抗生素具有耐药性。菌株对氧化铜纳米颗粒的MIC为250 μg/ml,对氯霉素抗生素的MIC为62.50 μg/ml。与抗生素相比,铜纳米颗粒对MIC的影响更大,但低于抗生素和氧化铜纳米颗粒的联合作用。结论。氧化铜纳米颗粒或氧化铜纳米颗粒与氯霉素抗生素的协同作用可有效降低MexA基因的表达。实际意义。纳米颗粒作为抗生素的替代或补充是一个重要的选择。此外,氧化铜纳米颗粒与抗生素联合使用时,可以更有效地抑制细菌生长。
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Synergistic effect of copper oxide nanoparticles and chloramphenicol antibiotic on MexA gene expression of pump efflux system in drug-resistant Pseudomonas aeruginosa isolates
Background. Pseudomonas aeruginosa is a causative agent of nosocomial infections. Chloramphenicol is a broad-spectrum, inexpensive, and common antibiotic. MexAB-OprM is a secretory pump that causes the innate resistance of this bacterium. This study aimed to evaluate the expression of MexA gene under the treatment of copper nanoparticles and chloramphenicol. Methods. In this study, 49 samples were collected from 11 laboratories in Mashhad, Iran.Abundance of Me gene MexA was done by polymerase chain reaction (PCR) method, and antibiotic susceptibility assessment was performed by disk diffusion method. To calculate minimal inhibitory concentration (MIC) and minimal bactericidal concentration (MBC), copper nanoparticles, and a combination of both, the broth dilution method was performed. Microdilution method and real time PCR technique were used to determine the effective dilution of copper oxide nanoparticles and chloramphenicol antibiotics and expression of MexA gene, respectively. Result. The identity of 49 strains was confirmed. All strains had the MexA gene and were resistant to more than two antibiotics. The MIC of bacterial strains was 250 μg/ml for copper oxide nanoparticles and 62.50 μg/ml for chloramphenicol antibiotic. Compared to antibiotics, copper nanoparticles had a greater effect on MIC, though it was lower than the combined effect of antibiotics and copper oxide nanoparticles. Conclusion. Copper oxide nanoparticles or the synergistic effect of copper oxide nanoparticles and chloramphenicol antibiotics are effective in reducing MexA gene expression. Practical Implications. Nanoparticles are an important option for use as an alternative to or supplement to antibiotics. Also, copper oxide nanoparticles are more effective to inhibit bacterial growth when used in combination with antibiotics.
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