首页> 外文期刊>Chemotherapy: International Journal of Experimental and Clinical Chemotherapy >Efflux pump overexpression in conjunction with alternation of outer membrane protein may induce Acinetobacter baumannii resistant to imipenem.
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Efflux pump overexpression in conjunction with alternation of outer membrane protein may induce Acinetobacter baumannii resistant to imipenem.

机译:外排泵过表达与外膜蛋白交替表达可能诱导鲍曼不动杆菌对亚胺培南具有抗性。

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BACKGROUND: To investigate the role of outer membrane proteins in Acinetobacter baumannii resistant to imipenem, 2 strains were procured from the same patient. METHODS: The imipenem-resistant strain was obtained following a period of imipenem treatment in vivo. The multilocus sequence typing and repetitive extragenic palindromic PCR results indicated that the imipenem-resistant strain originated from the sensitive one. RESULTS: Isoelectric focusing detected no carbapenemases, with neither OXA carbapenemases nor metallo-beta-lactamases found. Mass spectrophotometric analysis revealed that 3 outer membrane proteins were expressed differentially in the 2 strains: 2 downregulated proteins (OprD and CarO) and 1 upregulated the 34-kDa efflux pump protein in the resistant strain. A 32-fold decrease in the MIC for imipenem in the presence of Phe-Arg-beta-naphthylamide in the same strain indicated a possible involvement of the efflux pump mechanism in its resistance, which was consistent with the findings that the mRNA expression of the 34-kDa efflux pump gene was almost fivefold upregulated in the imipenem-resistant strain compared with that in the imipenem-sensitive strain. Such a significant difference, however, was not found in the expression of AdeB and AdeJ between the 2 strains, and AdeE was not detected. CONCLUSIONS: Our results suggested that downregulation of outer membrane proteins in conjunction with efflux pump overexpression might contribute to imipenem resistance induced in vivo in A. baumannii.
机译:背景:为了研究外膜蛋白在鲍曼不动杆菌对亚胺培南耐药中的作用,从同一名患者中采购了2株菌株。方法:经过一段时间的亚胺培南体内治疗后,获得了亚胺培南耐药菌株。多基因座序列分型和重复的外源回文PCR结果表明,亚胺培南耐药菌株起源于敏感菌株。结果:等电聚焦未检测到碳青霉烯酶,也未发现OXA碳青霉烯酶和金属β-内酰胺酶。质谱分析表明,在2个菌株中3种外膜蛋白表达差异:在抗性菌株中2个下调蛋白(OprD和CarO)和1个上调34 kDa外排泵蛋白。在同一菌株中存在Phe-Arg-β-萘酰胺的情况下,亚胺培南的MIC降低32倍,表明外排泵机制可能与其耐药有关,这与以下发现相符:与亚胺培南敏感菌株相比,亚胺培南耐药菌株的34 kDa外排泵基因几乎上调了五倍。然而,在两个菌株之间的AdeB和AdeJ的表达中未发现这种显着差异,并且未检测到AdeE。结论:我们的结果表明外膜蛋白的下调与外排泵的过度表达可能有助于鲍曼不动杆菌体内诱导的亚胺培南耐药。

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