Antibiotic Resistance Pattern and Evaluation of Metallo-Beta Lactamase Genes Including bla- IMP and bla- VIM Types in Pseudomonas aeruginosa Isolated from Patients in Tehran Hospitals.

ISRN Microbiology Pub Date : 2014-04-23 eCollection Date: 2014-01-01 DOI:10.1155/2014/941507
Samira Aghamiri, Nour Amirmozafari, Jalil Fallah Mehrabadi, Babak Fouladtan, Hossein Samadi Kafil
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引用次数: 40

Abstract

Beta-lactamase producing strains of Pseudomonas aeruginosa are important etiological agents of hospital infections. Carbapenems are among the most effective antibiotics used against Pseudomonas infections, but they can be rendered infective by group B β -lactamase, commonly called metallo-beta lactamase. In this study, the antimicrobial sensitivity patterns of P. aeruginosa strains isolated from 9 different hospitals in Tehran, Iran, as well as the prevalence of MBLs genes (bla- VIM and bla- IMP ) were determined. A total of 212 strains of P. aeruginosa recovered from patients in hospitals in Tehran were confirmed by both biochemical methods and PCR. Their antimicrobial sensitivity patterns were determined by Kirby-Bauer disk diffusion method. Following MIC determination, imipenem resistant strains were selected by DDST method which was followed by PCR tests for determination of MBLs genes: bla- IMP and bla- VIM . The results indicated that, in the DDST phenotypic method, among the 100 imipenem resistant isolates, 75 strains were MBLs positive. The PCR test indicated that 70 strains (33%) carried bla- VIM gene and 20 strains (9%) harbored bla- IMP . The results indicated that the extent of antibiotic resistance among Pseudomonas aeruginosa is on the rise. This may be due to production of MBLs enzymes. Therefore, determination of antibiotic sensitivity patterns and MBLs production by these bacteria, can be important in control of clinical Pseudomonas infection.

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德黑兰医院铜绿假单胞菌金属- β -内酰胺酶基因bla- IMP和bla- VIM的耐药模式及评价
产β -内酰胺酶的铜绿假单胞菌是医院感染的重要病原。碳青霉烯类是抗假单胞菌感染最有效的抗生素之一,但它们可以被B族β -内酰胺酶(通常称为金属β -内酰胺酶)感染。本研究对伊朗德黑兰9家不同医院分离的铜绿假单胞菌(P. aeruginosa)的抗菌药物敏感性及MBLs基因(bla- VIM和bla- IMP)的流行情况进行了测定。采用生化方法和PCR方法对德黑兰地区医院患者采集的212株铜绿假单胞菌进行鉴定。采用Kirby-Bauer纸片扩散法测定其药敏谱。MIC测定后,采用DDST法筛选耐亚胺培南菌株,PCR检测MBLs基因:bla- IMP和bla- VIM。结果表明,在DDST表型法中,100株亚胺培南耐药菌株中,有75株MBLs阳性。PCR检测结果显示,70株(33%)携带bla- VIM基因,20株(9%)携带bla- IMP基因。结果表明,铜绿假单胞菌的耐药程度呈上升趋势。这可能是由于MBLs酶的产生。因此,确定这些细菌的抗生素敏感性模式和MBLs的产生对控制临床假单胞菌感染很重要。
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