Aghamiri Samira, Amirmozafari Nour, Fallah Mehrabadi Jalil, Fouladtan Babak, Samadi Kafil Hossein
Department of Microbiology, Islamic Azad University, Lahijan Branch, Lahijan, Iran.
School of Medicine, Microbiology Department, Iran University of Medical Sciences, Tehran, Iran.
ISRN Microbiol. 2014 Apr 23;2014:941507. doi: 10.1155/2014/941507. eCollection 2014.
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.
产β-内酰胺酶的铜绿假单胞菌菌株是医院感染的重要病原体。碳青霉烯类是用于对抗铜绿假单胞菌感染的最有效抗生素之一,但它们可能会被B组β-内酰胺酶(通常称为金属β-内酰胺酶)灭活。在本研究中,测定了从伊朗德黑兰9家不同医院分离出的铜绿假单胞菌菌株的抗菌敏感性模式以及MBLs基因(bla-VIM和bla-IMP)的流行情况。通过生化方法和PCR对从德黑兰医院患者中分离出的总共212株铜绿假单胞菌进行了确认。通过 Kirby-Bauer 纸片扩散法测定其抗菌敏感性模式。在测定MIC后,通过双倍稀释法选择亚胺培南耐药菌株,随后进行PCR检测以确定MBLs基因:bla-IMP和bla-VIM。结果表明,在双倍稀释表型方法中,在100株亚胺培南耐药菌株中,75株MBLs呈阳性。PCR检测表明,70株(33%)携带bla-VIM基因,20株(9%)携带bla-IMP。结果表明,铜绿假单胞菌的抗生素耐药程度正在上升。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产生情况,对于控制临床铜绿假单胞菌感染可能很重要。