Evaluation of the β-Lactamase Disk Test Method in the Detection of Extended-Spectrum-β- Lactamases in Clinical Isolates of Multidrug-Resistant Pseudomonas aeruginosa

  • سال انتشار: 1394
  • محل انتشار: مجله دانشگاه علوم پزشکی کرمان، دوره: 22، شماره: 1
  • کد COI اختصاصی: JR_JKMU-22-1_001
  • زبان مقاله: انگلیسی
  • تعداد مشاهده: 123
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نویسندگان

Davood Kalantar-Neyestanaki

Assistant Professor, Department of Microbiology, Afzalipour School of Medicine, Kerman University of Medical Sciences, Kerman, Iran

Fereshteh Jabalameli

Assistant Professor, Department of Microbiology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran

Akbar Mirsalehian

Professor, Department of Microbiology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran

Mohammad Eman eini

Associate Professor, Department of Microbiology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran

چکیده

Background & Aims: The production of extended-spectrum-β-lactamases (ESBLs) is the main mechanism of resistance to β-lactam antibiotics. The outbreak of isolates simultaneously possessing several resistance mechanisms to β-lactam antibiotics caused a decrease in sensitivity of the confirmatory tests for ESBL. The aim of this study was the evaluation of the β-lactamase disk test method in the detection of ESBLs in clinical isolates of multidrug-resistant Pseudomonas aeruginosa. Methods: A total of ۱۰۰ multidrug-resistant P. aeruginosa isolates were recovered from burn patients. The sensitivity of the isolates to different antibiotics was determined using the standard disk diffusion method. ESBL-producing isolates were detected through the combination disk test with clavulanic acid, double disk synergy test, and β-lactamase disk test. Carbapenemase-producing isolates were detected using the Modified Hodge Test (MHT). The ESBLs genes (blaTEM, blaOXA, blaPER, blaSHV, blaCTX-M and blaPSE) were determined through polymerase chain reaction (PCR). Results: All isolates were multidrug resistant. Only ۳ isolates were detected as ESBL-producing isolates through combination disk test. No ESBL-producing isolates were detected through double disk synergy test. Among the ۱۰۰ studied isolates, ۸۷% were detected as ESBL-producing isolates and ۶۸% as carbpenemase-producing isolates through β-lactamase disk test. . The prevalence of blaTEM, blaOXA, and blaPER among isolates were ۹۷%, ۶۱%, and ۱۳%, respectively. All isolates were negative for blaSHV, blaPSE, and blaCTX-M. Conclusion: According to the results obtained in this study, the β-lactamase disk test is suitable for the detection of ESBLs in multidrug resistant isolates. However, further investigation is required

کلیدواژه ها

β-lactam resistance, Extended-spectrum-β-lactamases (ESBLs), Confirmatory tests, Pseudomonas aeruginosa, Burn

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