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Role of the Outer Membrane Protein OprD2 in Carbapenem-Resistance Mechanisms of Pseudomonas aeruginosa

机译:膜蛋白OprD2在铜绿假单胞菌碳青霉烯耐药机制中的作用

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We investigated the relationship between the outer membrane protein OprD2 and carbapenem-resistance in 141 clinical isolates of Pseudomonas aeruginosa collected between January and December 2013 from the First Affiliated Hospital of Anhui Medical University in China. Agar dilution methods were employed to determine the minimum inhibitory concentration of meropenem (MEM) and imipenem (IMP) for P. aeruginosa. The gene encoding OprD2 was amplified from141 P. aeruginosa isolates and analyzed by PCR and DNA sequencing. Differences between the effects of IMPR and IMPS groups on the resistance of the P. aeruginosa were observed by SDS-poly acrylamide gel electrophoresis (SDS-PAGE). Three resistance types were classified in the 141 carbapenem-resistant P. aeruginosa (CRPA) isolates tested, namely IMPRMEMR (66.7%), IMPRMEMS (32.6%), and IMPRMEMS (0.7%). DNA sequencing revealed significant diverse gene mutations in the OprD2-encoding gene in these strains. Thirty-four strains had large fragment deletions in the OprD2gene, in 6 strains the gene contained fragment inserts, and in 96 resistant strains, the gene featured small fragment deletions or multi-site mutations. Only 4 metallo-β-lactamase strains and 1 imipenem-sensitive (meropenem-resistant) strain showed a normal OprD2 gene. Using SDS-PAGE to detect the outer membrane protein in 16 CRPA isolates, it was found that 10 IMPRMEMR strains and 5 IMPRMEMS strains had lost the OprD2 protein, while the IMPSMEMR strain contained a normal 46-kDa protein. In conclusion, mutation or loss of the OprD2-encoding gene caused the loss of OprD2, which further led to carbapenem-resistance of P. aeruginosa. Our findings provide insights into the mechanism of carbapenem resistance in P. aeruginosa.
机译:我们调查了2013年1月至2013年12月从中国安徽医科大学附属第一医院采集的141株铜绿假单胞菌临床分离株中外膜蛋白OprD2与碳青霉烯耐药性的关系。琼脂稀释法用于确定美洛培南(MEM)和亚胺培南(IMP)对铜绿假单胞菌的最小抑制浓度。从141个铜绿假单胞菌分离物中扩增了编码OprD2的基因,并通过PCR和DNA测序进行了分析。通过SDS-聚丙烯酰胺凝胶电泳(SDS-PAGE)观察到IMP R 和IMP S 基团对铜绿假单胞菌抗性的影响存在差异。在测试的141个对碳青霉烯耐药的铜绿假单胞菌(CRPA)菌株中分类了三种耐药类型,即IMP R MEM R (66.7%),IMP R < / sup> MEM S (32.6%)和IMP R MEM S (0.7%)。 DNA测序显示,这些菌株的OprD2编码基因中存在明显的多种基因突变。 34个菌株在OprD2基因中具有大片段缺失,在6个菌株中该基因包含片段插入,在96个抗性菌株中,该基因具有小片段缺失或多位点突变的特征。只有4个金属-β-内酰胺酶菌株和1个对亚胺培南敏感(美洛培南耐药)的菌株显示正常的OprD2基因。用SDS-PAGE检测16株CRPA分离株的外膜蛋白,发现10株IMP R MEM R 菌株和5株IMP R 菌株MEM S 菌株丢失了OprD2蛋白,而IMP S MEM R 菌株含有正常的46 kDa蛋白。总之,编码OprD2的基因发生突变或丢失会导致OprD2的丢失,从而进一步导致铜绿假单胞菌对碳青霉烯的耐药。我们的发现为铜绿假单胞菌对碳青霉烯耐药的机制提供了见解。

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