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Journal of Clinical Microbiology, September 2005, p. 4541-4544, Vol. 43, No. 9
0095-1137/05/$08.00+0     doi:10.1128/JCM.43.9.4541-4544.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Correlation of Penicillin Binding Protein 2a Detection with Oxacillin Resistance in Staphylococcus aureus and Discovery of a Novel Penicillin Binding Protein 2a Mutation

Adam M. Bressler,1 Teresa Williams,2 Elizabeth E. Culler,1 Wenming Zhu,3 David Lonsway,3 Jean B. Patel,3 and Frederick S. Nolte1*

Department of Pathology and Laboratory Medicine, Emory University School of Medicine,1 Clinical Microbiology Laboratory, Emory University Hospital,2 Division of Healthcare Quality Promotion, Centers for Disease Control and Prevention, Atlanta, Georgia3

Received 10 March 2005/ Returned for modification 25 May 2005/ Accepted 14 June 2005

We compared a rapid slide latex agglutination test (LAT; Oxoid, Basingstoke, United Kingdom) that detects penicillin binding protein 2a (PBP2a) with MicroScan conventional panels (Dade Behring, West Sacramento, CA) for detection of oxacillin resistance in Staphylococcus aureus. The PBP2a LAT demonstrated 99% agreement with MicroScan oxacillin MIC results for 388 isolates of S. aureus. All 249 oxacillin-resistant isolates gave strong positive reactions in the LAT (100% sensitivity). Three of the 139 oxacillin-susceptible isolates were also strongly positive and one was weakly positive in the LAT (97.1% specificity). The three oxacillin-susceptible isolates with strongly positive reactions were further characterized. The mecA gene was detected in all three by PCR; one isolate was determined to be resistant to oxacillin by reference broth microdilution testing (MIC, 8 µg/ml), one isolate was inducibly resistant to oxacillin (MIC of 16 µg/ml after overnight induction), and one isolate remained susceptible regardless of the method used for testing. Sequence analysis of a 2.1-kb gene fragment of the mecA gene from the susceptible isolate revealed a one-base substitution at nucleotide position 1449 which results in a Met-to-Ile change for amino acid residue 483. This amino acid substitution has not been previously reported and may be associated with a change in the function of PBP2a resulting in oxacillin susceptibility. An additional 487 isolates were tested in parallel with the both the LAT and MicroScan panels using criteria in which only strong (3 to 4+) or repeatedly weak (1 to 2+) LAT reactions were considered positive, and the results showed 99.4% agreement. The PBP2a LAT provided rapid and reliable detection of oxacillin resistance and proved a useful adjunct to the phenotypic method. Both methods provided reliable detection of oxacillin-resistant S. aureus and facilitated the discovery of a novel, functionally impaired form of PBP2a.


* Corresponding author. Mailing address: Emory University Hospital, Room F145, 1364 Clifton Road NE, Atlanta, GA 30322. Phone: (404) 712-7297. Fax: (404) 712-4632. E-mail: fnolte{at}emory.edu.


Journal of Clinical Microbiology, September 2005, p. 4541-4544, Vol. 43, No. 9
0095-1137/05/$08.00+0     doi:10.1128/JCM.43.9.4541-4544.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.




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