Rapid detection of ESBL, carbapenemases, MRSA and other important resistance phenotypes within 6-8 h by automated disc diffusion antibiotic susceptibility testing

Autor: Marion Jetter, Natalia Kolesnik-Goldmann, Erik C. Böttger, Nicolas Blöchliger, Michael Hombach, Peter M. Keller
Přispěvatelé: University of Zurich, Hombach, Michael
Jazyk: angličtina
Rok vydání: 2017
Předmět:
0301 basic medicine
Microbiology (medical)
Methicillin-Resistant Staphylococcus aureus
Staphylococcus aureus
Time Factors
Klebsiella pneumoniae
medicine.drug_class
Staphylococcus
030106 microbiology
Antibiotics
610 Medicine & health
Microbial Sensitivity Tests
medicine.disease_cause
beta-Lactamases
2726 Microbiology (medical)
Incubation period
Microbiology
03 medical and health sciences
Bacterial Proteins
Enterobacteriaceae
Staphylococcus epidermidis
Enterobacter cloacae
medicine
Escherichia coli
Humans
2736 Pharmacology (medical)
Pharmacology (medical)
Escherichia coli Infections
Pharmacology
Automation
Laboratory

biology
10179 Institute of Medical Microbiology
Enterobacteriaceae Infections
2725 Infectious Diseases
Staphylococcal Infections
biology.organism_classification
Anti-Bacterial Agents
Infectious Diseases
Phenotype
3004 Pharmacology
570 Life sciences
DOI: 10.5167/uzh-141752
Popis: Background In principle, automated systems allow rapid reading of disc diffusion AST (rAST) within 6-8 h. Objectives This study analysed whether rAST can discriminate resistance phenotypes such as ESBL, carbapenemases and MRSA/methicillin-resistant Staphylococcus epidermidis from WT populations. We describe species-drug combinations that may require clinical breakpoint adaptions for early reading due to zone diameter changes during the incubation period. Methods In total, 1852 clinical strains [Escherichia coli (n = 475), Klebsiella pneumoniae (n = 375), Enterobacter cloacae (n = 301), Staphylococcus aureus (n = 407) and S. epidermidis (n = 294)] were included in this study comprising WT populations and important resistance phenotypes, e.g. ESBL, carbapenemases and MRSA. We assessed (i) separation of resistance phenotypes and WT populations after 6, 8 and 12 h as compared with the 18 h standard, and (ii) diameter changes of WT populations and associated putative epidemiological cut-offs during the incubation period. Disc diffusion plates were automatically streaked, incubated and imaged using the WASPLabTM system. Results and conclusions We demonstrated that important resistance phenotypes could reliably be separated from WT populations at early reading times for the most prevalent bacterial pathogens encountered in the clinical laboratory. Current AST expert rules and algorithms for identification of resistance mechanisms can readily be applied for rAST, e.g. EUCAST recommended rules for detection of ESBL, AmpC, carbapenemases and MRSA/methicillin-resistant S. epidermidis. However, several species-drug combinations may require clinical breakpoint adaptations when using rAST as the diameter, and hence the epidemiological cut-off, changes during the incubation period.
Databáze: OpenAIRE