title

روش فنوتیپی Imipenem-EDTA برای تشخیص پسودوموناس آیروژینوزای تولید کننده متالوبتالاکتاماز در اراک

رحیمی, بهاره and برون, فرخ and شجاع پور, مانا and صادقی, عبدالرحیم (1391) روش فنوتیپی Imipenem-EDTA برای تشخیص پسودوموناس آیروژینوزای تولید کننده متالوبتالاکتاماز در اراک. در: The 13th Iranian & The Second International Congress of Microbiology, July 14 – 16, 2012, Ardabil - Iran.

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Title

Imipenem-EDTA Disk Methods for Detecting Metallo-β-Lactamase-Producing Pseudomonas aeruginosa in Arak

English Abstract

Background & Objectives: Pseudomonas aeruginosa is a life-threatening agent for immuno-compromised patients. This gram negative bacterium is resistant to the various antibiotics. Until now several resistance mechanisms in P. aeruginosa have been known, Metallo-β-lactamase (MBL) production is one of the significant mechanisms in antibiotic resistance. We aimed to determine frequency of MBL-producing P. aeruginosa in Arak. Methods: In this study 108 strains were obtained from different clinical samples of hospitalized patients in Arak hospitals. After identifing P. aeruginosa strains by microbiological tests, antibiotic susceptibility test was done for imipenem by disk diffiusion Methods according to NCCLS (National Committee for Clinical Laboratory Standards). Imipenem-EDTA was performed for imipenem-resistant strains. A 0.5 M EDTA solution was prepared by dissolving 186.1 g of disodium EDTA .2H2O in 1000 ml of distilled water and adjusting it to pH 8.0 by using NaOH. The mixture was sterilized, then imipenem disk contained EDTA was dried in an incubator. Two 10 mg imipenem disks were placed on the surface of an agar plate and EDTA solution was added to one of them to obtain concentration of 930 µg. The inhibition zones of imipenem and imipenem-EDTA disks were compared after 16-18 h of incubation at 35oC. Enhancement in inhibition zone (≥7 mm) for imipenem-EDTA disk is referred to MBL positive (4, 5). Results: Among 108 P. aeruginosa isolates 40 strains were resistant to imipenem. 20 out of 40 imipenem-resistant strains showed MBL positive. Conclusion: Results illustrated half of imipenem-resistant strains were MBL positive. Therefore it is important to detect MBL-producing strains due to control their transmission. In addition phenotypic detection of MBLs is not an accurate Methods, molecular studies could reveal more accurate data.

Item Type:Conference or Workshop Item (Poster)
زبان سند : انگلیسی
نویسنده مسئول :بهاره رحیمی
کلیدواژه ها (انگلیسی):EDTA ; Imipenem ; Metallo Beta Lactamase ; Pseudomonas aeruginosa
Subjects:WA Public Health > WA 30 Social, Economic, and Environmental factor in public health
WA Public Health > WA 30 Social, Economic, and Environmental factor in public health

QW Microbiology and Immunology
WA Public Health
WA Public Health

WF Respiratory System
Divisions:Vice Chancellor for Research and Technology > Deputy for Research and Technology management and Medical Information > University of Management Conferences and Congresses
ID Code:4898
Deposited By: MS Soghra Golmaghani
Deposited On:21 Aug 1392 10:12
Last Modified:21 Aug 1392 10:41

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