Rapid real-time PCR for the detection of IMP, NDM, VIM, KPC and OXA-48 carbapenemase genes in isolates and spiked stool samples
Author:
Publisher
Elsevier BV
Subject
Infectious Diseases,Microbiology (medical),General Medicine
Reference22 articles.
1. Performance of the BD MAX instrument with check-direct CPE real-time PCR for the detection of carbapenemase genes from rectal swabs, in a setting with endemic dissemination of carbapenemase-producing enterobacteriaceae;Antonelli;Diagn Microbiol Infect Dis,2016
2. Tracing of false negative results in phenotypic methods for identification of carbapenemase by real-time PCR;Azimi;Gene,2016
3. Real-time PCR assay allows detection of the new delhi metallo-beta-lactamase (NDM-1)-encoding gene in france;Diene;Int J Antimicrob Agents,2011
4. Multicentre evaluation of a real-time PCR assay to detect genes encoding clinically relevant carbapenemases in cultured bacteria;Ellington;Int J Antimicrob Agents,2016
5. Rapid detection of blaKPC carbapenemase genes by real-time PCR;Hindiyeh;J Clin Microbiol,2008
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2. Enhanced detection for antibiotic resistance genes in wastewater samples using CRISPR-enriched metagenomic method;2024-07-31
3. Development of a multiplex real-time PCR assay for simultaneous detection of common colistin and carbapenemase genes;Vietnam Journal of Science and Technology;2024-04-10
4. Rapid Detection of New Delhi Metallo-β-Lactamase Gene Using Recombinase-Aided Amplification Directly on Clinical Samples From Children;Frontiers in Microbiology;2021-07-22
5. Fast and automated detection of common carbapenemase genes using multiplex real-time PCR on the BD MAX™ system;Journal of Microbiological Methods;2021-06
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