Skip to main content
Antimicrobial Agents and Chemotherapy logoLink to Antimicrobial Agents and Chemotherapy
. 1995 Apr;39(4):982–984. doi: 10.1128/aac.39.4.982

Revised interpretation of oxacillin MICs for Staphylococcus epidermidis based on mecA detection.

C L McDonald 1, W E Maher 1, R J Fass 1
PMCID: PMC162666  PMID: 7786008

Abstract

In 1992 and 1993, at The Ohio State University Medical Center, a larger proportion of Staphylococcus epidermidis strains required oxacillin MICs of 1 to 2 micrograms/ml than did Staphylococcus aureus strains. mecA genotype was correlated with antimicrobial susceptibility for selected clinical S. epidermidis strains. All 14 strains that required oxacillin MICs of < or = 0.25 microgram/ml and 2 of 5 strains that required oxacillin MICs of 0.5 microgram/ml were susceptible by 1-microgram oxacillin disk test and were mecA negative. Three of 5 strains that required oxacillin MICs of 0.5 microgram/ml and all 18 strains that required oxacillin MICs of > or = 1.0 microgram/ml were resistant by oxacillin disk test and were mecA positive. Current National Committee for Clinical Laboratory Standards MIC interpretive criteria may underestimate methicillin resistance among S. epidermidis strains.

Full Text

The Full Text of this article is available as a PDF (191.7 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Archer G. L., Pennell E. Detection of methicillin resistance in staphylococci by using a DNA probe. Antimicrob Agents Chemother. 1990 Sep;34(9):1720–1724. doi: 10.1128/aac.34.9.1720. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Brakstad O. G., Maeland J. A., Tveten Y. Multiplex polymerase chain reaction for detection of genes for Staphylococcus aureus thermonuclease and methicillin resistance and correlation with oxacillin resistance. APMIS. 1993 Sep;101(9):681–688. doi: 10.1111/j.1699-0463.1993.tb00165.x. [DOI] [PubMed] [Google Scholar]
  3. Fass R. J., Helsel V. L., Barnishan J., Ayers L. W. In vitro susceptibilities of four species of coagulase-negative staphylococci. Antimicrob Agents Chemother. 1986 Oct;30(4):545–552. doi: 10.1128/aac.30.4.545. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Geha D. J., Uhl J. R., Gustaferro C. A., Persing D. H. Multiplex PCR for identification of methicillin-resistant staphylococci in the clinical laboratory. J Clin Microbiol. 1994 Jul;32(7):1768–1772. doi: 10.1128/jcm.32.7.1768-1772.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Heath L. S., Sloan G. L., Heath H. E. A simple and generally applicable procedure for releasing DNA from bacterial cells. Appl Environ Microbiol. 1986 May;51(5):1138–1140. doi: 10.1128/aem.51.5.1138-1140.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Levenson C., Watson R., Sheldon E. L. Biotinylated psoralen derivative for labeling nucleic acid hybridization probes. Methods Enzymol. 1990;184:577–583. [PubMed] [Google Scholar]
  7. Ligozzi M., Rossolini G. M., Tonin E. A., Fontana R. Nonradioactive DNA probe for detection of gene for methicillin resistance in Staphylococcus aureus. Antimicrob Agents Chemother. 1991 Mar;35(3):575–578. doi: 10.1128/aac.35.3.575. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Madiraju M. V., Brunner D. P., Wilkinson B. J. Effects of temperature, NaCl, and methicillin on penicillin-binding proteins, growth, peptidoglycan synthesis, and autolysis in methicillin-resistant Staphylococcus aureus. Antimicrob Agents Chemother. 1987 Nov;31(11):1727–1733. doi: 10.1128/aac.31.11.1727. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Maher W. E., Kobe M., Fass R. J. Restriction endonuclease analysis of clinical Pseudomonas aeruginosa strains: useful epidemiologic data from a simple and rapid method. J Clin Microbiol. 1993 Jun;31(6):1426–1429. doi: 10.1128/jcm.31.6.1426-1429.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Murakami K., Minamide W., Wada K., Nakamura E., Teraoka H., Watanabe S. Identification of methicillin-resistant strains of staphylococci by polymerase chain reaction. J Clin Microbiol. 1991 Oct;29(10):2240–2244. doi: 10.1128/jcm.29.10.2240-2244.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Olsson-Liljequist B., Larsson P., Ringertz S., Löfdahl S. Use of a DNA hybridization method to verify results of screening for methicillin resistance in staphylococci. Eur J Clin Microbiol Infect Dis. 1993 Jul;12(7):527–533. doi: 10.1007/BF01970958. [DOI] [PubMed] [Google Scholar]
  12. Predari S. C., Ligozzi M., Fontana R. Genotypic identification of methicillin-resistant coagulase-negative staphylococci by polymerase chain reaction. Antimicrob Agents Chemother. 1991 Dec;35(12):2568–2573. doi: 10.1128/aac.35.12.2568. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Saffran W. A., Welsh J. T., Knobler R. M., Gasparro F. P., Cantor C. R., Edelson R. L. Preparation and characterization of biotinylated psoralen. Nucleic Acids Res. 1988 Aug 11;16(15):7221–7231. doi: 10.1093/nar/16.15.7221. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Sierra-Madero J. G., Knapp C., Karaffa C., Washington J. A. Role of beta-lactamase and different testing conditions in oxacillin-borderline-susceptible staphylococci. Antimicrob Agents Chemother. 1988 Dec;32(12):1754–1757. doi: 10.1128/aac.32.12.1754. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Thompson J. D., Cuddy K. K., Haines D. S., Gillepsie D. Extraction of cellular DNA from crude cell lysate with glass. Nucleic Acids Res. 1990 Feb 25;18(4):1074–1074. doi: 10.1093/nar/18.4.1074. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Thornsberry C., Caruthers J. Q., Baker C. N. Effect of temperature on the in vitro susceptibility of Staphylococcus aureus to penicillinase-resistant penicillins. Antimicrob Agents Chemother. 1973 Sep;4(3):263–269. doi: 10.1128/aac.4.3.263. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Tokue Y., Shoji S., Satoh K., Watanabe A., Motomiya M. Comparison of a polymerase chain reaction assay and a conventional microbiologic method for detection of methicillin-resistant Staphylococcus aureus. Antimicrob Agents Chemother. 1992 Jan;36(1):6–9. doi: 10.1128/aac.36.1.6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Ubukata K., Nakagami S., Nitta A., Yamane A., Kawakami S., Sugiura M., Konno M. Rapid detection of the mecA gene in methicillin-resistant staphylococci by enzymatic detection of polymerase chain reaction products. J Clin Microbiol. 1992 Jul;30(7):1728–1733. doi: 10.1128/jcm.30.7.1728-1733.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Unal S., Hoskins J., Flokowitsch J. E., Wu C. Y., Preston D. A., Skatrud P. L. Detection of methicillin-resistant staphylococci by using the polymerase chain reaction. J Clin Microbiol. 1992 Jul;30(7):1685–1691. doi: 10.1128/jcm.30.7.1685-1691.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Antimicrobial Agents and Chemotherapy are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES