Results of Disk Diffusion Testing with Cefoxitin Correlate with Presence of mecA in Staphylococcus spp
- 1 August 2005
- journal article
- Published by American Society for Microbiology in Journal of Clinical Microbiology
- Vol. 43 (8), 3818-23
- https://doi.org/10.1128/jcm.43.8.3818-3823.2005
Abstract
The cefoxitin disk diffusion (DD) test for predicting mecA- mediated oxacillin resistance in staphylococci was assessed during a three-phase study. In phase 1, one laboratory tested 62 and 53 strains of Staphylococcus aureus and coagulase-negative staphylococci (CoNS), respectively. These data were used to choose the provisional cefoxitin DD breakpoints (resistant/susceptible) of ≤19 mm/≥20 mm for S. aureus and ≤24 mm/≥25 mm for CoNS for the next phase of testing. In phase 2, 10 laboratories each tested approximately 40 in-house strains of staphylococci (half of which were S. aureus ) using Mueller-Hinton agar from different manufacturers. In this phase, the sensitivity and specificity, respectively, of the cefoxitin disk test were 98 and 100% for S. aureus and 99 and 96% for CoNS. The cefoxitin DD test performed equivalently to oxacillin broth microdilution (BMD) and to oxacillin DD tests among S. aureus and mecA -positive CoNS strains but gave better results than oxacillin BMD or oxacillin DD for mecA -negative strains of CoNS. The cefoxitin DD test also was much easier to read and did not require the use of transmitted light for detection of resistance. Based on data from the first two phases, the Clinical and Laboratory Standards Institute (CLSI; formerly NCCLS) adopted the use of the cefoxitin DD test for predicting mecA- mediated oxacillin resistance in staphylococci and revised Table 2C in CLSI document M100-S14 to reflect the change. In the third phase, an additional 61 challenge strains of CoNS for which the oxacillin MICs were 0.5 to 2 μg/ml were tested in a single laboratory to determine the effectiveness of the cefoxitin DD test for this group of borderline-resistant isolates. These data were used to refine the description of the test in CLSI document M100-S15. The cefoxitin DD test is preferred over the oxacillin DD test for predicting mecA -mediated oxacillin resistance in S. aureus and CoNS.Keywords
This publication has 15 references indexed in Scilit:
- A Clone of Methicillin-ResistantStaphylococcus aureusamong Professional Football PlayersNew England Journal of Medicine, 2005
- Evaluation of a cefoxitin disk diffusion test for the routine detection of methicillin-resistant Staphylococcus aureusClinical Microbiology & Infection, 2004
- Evaluation of a disk diffusion method with cefoxitin (30 μg) for detection of methicillin-resistant Staphylococcus aureusEuropean Journal of Clinical Microbiology & Infectious Diseases, 2004
- Evaluation of a cefoxitin 30 g disc on Iso-Sensitest agar for detection of methicillin-resistant Staphylococcus aureusJournal of Antimicrobial Chemotherapy, 2003
- Evaluation of Three Techniques for Detection of Low-Level Methicillin-Resistant Staphylococcus aureus (MRSA): a Disk Diffusion Method with Cefoxitin and Moxalactam, the Vitek 2 System, and the MRSA-Screen Latex Agglutination TestJournal of Clinical Microbiology, 2002
- Transcription of the Gene Mediating Methicillin Resistance in Staphylococcus aureus ( mecA ) Is Corepressed but Not Coinduced by Cognate mecA and β-Lactamase RegulatorsJournal of Bacteriology, 2001
- Optimal Inoculation Methods and Quality Control for the NCCLS Oxacillin Agar Screen Test for Detection of Oxacillin Resistance in Staphylococcus aureusJournal of Clinical Microbiology, 2001
- Performance of Eight Methods, Including Two New Rapid Methods, for Detection of Oxacillin Resistance in a Challenge Set of Staphylococcus aureu s OrganismsJournal of Clinical Microbiology, 2001
- Stable classes of phenotypic expression in methicillin-resistant clinical isolates of staphylococciAntimicrobial Agents and Chemotherapy, 1991
- New mechanism for methicillin resistance in Staphylococcus aureus: clinical isolates that lack the PBP 2a gene and contain normal penicillin-binding proteins with modified penicillin-binding capacityAntimicrobial Agents and Chemotherapy, 1989