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首页> 外文期刊>New Microbes and New Infections >Insertional inactivation of oprD in carbapenem-resistant Pseudomonas aeruginosa strains isolated from burn patients in Tehran, Iran
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Insertional inactivation of oprD in carbapenem-resistant Pseudomonas aeruginosa strains isolated from burn patients in Tehran, Iran

机译:从伊朗德黑兰烧伤患者中分离出的耐碳青霉烯的铜绿假单胞菌铜绿假单胞菌菌株中oprD的插入失活

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In this study, we report the insertion sequence IS Ppu 21 in the opr D porin gene of carbapenem-resistant Pseudomonas aeruginosa isolates from burn patients in Tehran, Iran. Antibiotic susceptibility tests for P.?aeruginosa isolates were determined. Production of metallo-β-lactamases (MBLs) and carbapenemase was evaluated and the β-lactamase-encoding and aminoglycoside-modifying enzyme genes were investigated by PCR and sequencing methods. The mRNA transcription level of oprD and mex efflux pump genes were evaluated by real-time PCR. The outer membrane protein pro?le was determined by SDS–PAGE. The genetic relationship between the P.?aeruginosa isolates was assessed by random amplified polymorphic DNA PCR. In all, 10.52% (10/95) of clinical isolates of P.?aeruginosa harboured the IS Ppu 21 insertion element in the opr D gene. The extended-spectrum β-lactamase-encoding gene in IS Ppu 21-carrying isolates was bla TEM. PCR assays targeting MBL and carbapenemase-encoding genes were also negative in all ten isolates. The rmt A, aad A, aad B and arm A genes were positive in all IS Ppu 21 harbouring isolates. The relative expression levels of the mex X, mex B, mex T and mex D genes in ten isolates ranged from 0.1- to 1.4-fold, 1.1- to 3.68-fold, 0.3- to 8.22-fold and 1.7- to 35.17-fold, respectively. The relative expression levels of the oprD in ten isolates ranged from 0.57- to 35.01-fold, which was much higher than those in the control strain P.?aeruginosa PAO1. Evaluation of the outer membrane protein by SDS–PAGE suggested that opr D was produced at very low levels by all isolates. Using random amplified polymorphic DNA PCR genotyping, eight of the ten isolates containing IS Ppu 21 were shown to be clonally related. The present study describes a novel molecular mechanism, IS Ppu 21 insertion of the opr D gene, associated with carbapenem resistance in clinical P.?aeruginosa isolates.
机译:在这项研究中,我们报道了伊朗德黑兰烧伤患者对碳青霉烯耐药的铜绿假单胞菌分离株的opr D孔蛋白基因中的插入序列IS Ppu 21。测定了铜绿假单胞菌分离物的抗生素敏感性测试。评价了金属β-内酰胺酶(MBL)和碳青霉烯酶的产生,并通过PCR和测序方法研究了β-内酰胺酶编码和氨基糖苷修饰酶基因。通过实时PCR评估oprD和mex外排泵基因的mRNA转录水平。外膜蛋白谱通过SDS-PAGE测定。通过随机扩增的多态性DNA PCR评估铜绿假单胞菌分离物之间的遗传关系。总共有10.52%(10/95)的绿脓杆菌临床分离株在opr D基因中具有IS Ppu 21插入元件。携带IS Ppu 21的分离株的广谱β-内酰胺酶编码基因为bla TEM 。在所有十个分离物中,针对MBL和碳青霉烯酶编码基因的PCR检测结果均为阴性。 rmt A,aad A,aad B和arm A基因在所有带有IS Ppu 21的分离株中均为阳性。 mex X,mex B,mex T和mex D基因在十个分离物中的相对表达水平为0.1到1.4倍,1.1到3.68倍,0.3到8.22倍和1.7到35.17倍, 分别。十个分离株中oprD的相对表达水平在0.57至35.01倍之间,远高于对照菌株P.?aruginosa PAO1。通过SDS-PAGE对外膜蛋白的评估表明,所有分离物均以极低的水平产生oprD。使用随机扩增多态性DNA PCR基因分型,包含IS Ppu 21的十个分离株中有八个显示出克隆相关性。本研究描述了一种新的分子机制,即opr D基因的IS Ppu 21插入,与临床P.aeruginosa分离物中的碳青霉烯耐药有关。

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