Aim: To evaluate the diagnostic performance of MDI and temocillin disk (30 μg) for detection of carbapenem-resistant in comparison to real-time PCR.
Material And Methods: Fifty specimens submitted to the Microbiology Laboratory of Ain Shams University Hospitals and showed resistance to carbapenem drugs through routine culture and susceptibility testing, were assessed by both temocillin disk (30 μg) and MDI set to detect carbapenem-resistant . Results were compared to real-time PCR for detection of carbapenemase genes -48-, , and .
Results: Our work revealed that most of the CPE isolates were Klebsiella species (62%) followed by (24%), (10%) and (4%). Phenotypic detection of carbapenem-resistant classes revealed OXA - 48 in 96% of isolates, followed by MBLs (82%), and KPC (34%). All isolates were negative for . Detection of the genes by real-time PCR showed that the predominance was for the gene (96%) then (94%) followed by (54%), (46%) and finally (40%). Evaluation of the MDI set against PCR showed sensitivity (82.1%) and specificity (70%). The temocillin disk had 97.9% sensitivity and 50% specificity. The evaluation of Temocillin disk and MDI in combination for detection of carbapenem-resistant Enterobacteriaceae showed 99.7% sensitivity and 35% specificity.
Conclusion: Adding Temocillin disk to Mastdisks ID inhibitor combination set provides a simple, easy, rapid and highly sensitive test that can be used for screening and classification of carbapenem-resistant . However, it still needs confirmation by molecular techniques.
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http://dx.doi.org/10.3889/oamjms.2018.090 | DOI Listing |
Eur J Clin Microbiol Infect Dis
December 2023
Laboratory of Clinical Microbiology, CHU UCL Namur, UCLouvain, Site Godinne, Avenue Gaston Therasse, 1, 5530, Yvoir, Belgium.
Accurate susceptibility result of temocillin (TMO) is important for treating infections caused by multidrug-resistant Enterobacterales. This multicenter study aimed to investigate the performance of routine temocillin testing assays against Enterobacterales challenging strains. Forty-seven selected clinical isolates were blindly analyzed by 12 Belgian laboratories using VITEK® 2 (n = 5) and BD Phoenix™ (n = 3) automated systems, ETEST® gradient strip (n = 3), and disk (3 brands) diffusion method (DD; n = 6) for temocillin susceptibility using standardized methodology.
View Article and Find Full Text PDFJ Infect Dev Ctries
May 2023
Department of Medical Biology, Gaziantep University School of Medicine, Gaziantep, Turkey.
Introduction: Infections due to carbapenem-resistant Enterobacteriales, which have increased worldwide in recent years, cause concern. This study aimed to rapidly detect carbapenemase gene region by using flow cytometry in Enterobacteriales isolates and to evaluate its efficiency and susceptibility by comparing it with polymerase chain reaction (PCR).
Methodology: In the study, 21 isolates obtained from the blood cultures of patients hospitalized in intensive care units and found to intermediate or resistant to at least one carbapenem in the automated system, and 14 isolates belonging to the carbapenem-susceptible Enterobacteriales family were included.
Future Microbiol
July 2022
Institute of Cardiology, Lithuanian University of Health Sciences, Kaunas, LT-50161, Lithuania.
ESBL-producing and bacterial biofilms-forming are associated with antimicrobial treatment failure. This study aimed to investigate the phenotypic resistance mechanisms of CTX-M against old antibiotics - cell wall synthesis inhibitors temocillin, nitrofurantoin and fosfomycin. Susceptibility to old antibiotics testing was performed using disk diffusion method, biofilm formation was evaluated spectrophotometrically, and PCR was used for the determination of CTX-M type.
View Article and Find Full Text PDFMicrob Drug Resist
October 2020
Student Research Club at Department of Microbiology, Ludwik Rydygier Collegium Medicum, Nicolaus Copernicus University, Bydgoszcz, Poland.
This study evaluated the diagnostic performance of the eazyplex SuperBug CRE (eSBCRE) system, based on a loop-mediated isothermal amplification (LAMP), for the detection of the most common extended-spectrum beta-lactamases (ESBL) and carbapenemase genes in 140 clinical isolates of . ESBL ( and ) and carbapenemase (, , , , and ) genes were detected using the eSBCRE test and compared with the results obtained by PCR, real-time PCR, and phenotypic methods. Concordant results of 100% between PCR/real-time PCR and eSBCRE assays were observed.
View Article and Find Full Text PDFAfr Health Sci
June 2019
Faculty of Medicine Ibn Al Jazzar, Sousse, University of Sousse, Tunisia.
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