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首页> 外文期刊>Al Ameen Journal of Medical Sciences >Characterization of phenotypically metallo-??-lactamase positive Pseudomonas aeruginosa human isolates from Himachal Pradesh for MBL genes (blaVIM-2 and blaIMP-1), integrase gene class 1, 2, 3 (int1, int2 and int3) and sulphonamide resistance gene (sul1)
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Characterization of phenotypically metallo-??-lactamase positive Pseudomonas aeruginosa human isolates from Himachal Pradesh for MBL genes (blaVIM-2 and blaIMP-1), integrase gene class 1, 2, 3 (int1, int2 and int3) and sulphonamide resistance gene (sul1)

机译:表型典型的金属-β-内酰胺酶阳性铜绿假单胞菌人分离株从喜马al尔邦分离到MBL基因(blaVIM-2和blaIMP-1),整合酶1、2、3类(int1,int2和int3)和磺酰胺抗性基因( sul1)

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Background & objectives: The present study highlights the occurrence of MBL gene (bla VIM-2 ), integron class 1 (int1) and sulphonamide resistance (sul1) genes in P. aeruginosa iso lates recovered from patients of Shimla region of India. Methods: P. aeruginosa isolates detected positive for MBL by Combined Disc and Ezy MIC tests were characterized by PCR amplification of segments of bla IMP-1 and bla VIM-2 , integrase genes encoding integron classes int1, int2 and int3, and sul1 gene. The nucleotide sequence homologies with the published sequences of Pseudomonas spp and other gram-negative bacilli were determined. Results: All the confirmed isolates of P. aeruginosa were further subjected to nucleotide sequencing of 16SrRNA amplicons. MBL gene (bla VIM-2) was amplified in six out of 27 MBL positive isolates, int1 gene in eleven and sul1 gene in 14 MBL positive isolates .Only one isolate Pa138 carried both bla VIM-2 and int1 genes. The specificity was established b y nucleotide sequencing of the amplicons. Interpretation & Conclusion: The occurrence of bla VIM- 2, int1 and sul1 genes has been reported in the P. aeruginosa isolates of Shimla region of Himachal Pradesh. The studies might be useful to the clinicians for selecting suitable antibiotic for treating and controlling P. aeruginosa infections in this region.
机译:背景与目的:本研究突出显示了从印度西姆拉地区患者身上分离出的铜绿假单胞菌等位基因中存在MBL基因(bla VIM-2),整合子1类(int1)和磺酰胺抗性(sul1)基因的情况。方法:通过PCR扩增bla IMP-1和bla VIM-2片段,整合素基因整合型int1,int2和int3以及sul1基因,对MBL阳性的铜绿假单胞菌分离株进行检测。确定与已公布的假单胞菌属和其他革兰氏阴性杆菌序列的核苷酸序列同源性。结果:所有确认的铜绿假单胞菌分离物均经过16SrRNA扩增子的核苷酸测序。在27个MBL阳性分离株中,有6个扩增了MBL基因(bla VIM-2),在11个MBL阳性分离株中扩增了int1基因,在14个MBL阳性分离株中扩增了sul1基因。只有一个Pa138菌株同时携带bla VIM-2和int1基因。通过扩增子的核苷酸测序确定特异性。解释与结论:在喜马al尔邦西姆拉地区的铜绿假单胞菌分离株中已经报道了bla VIM-2,int1和sul1基因的发生。该研究对于临床医生选择合适的抗生素来治疗和控制该地区的铜绿假单胞菌感染可能是有用的。

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