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Journal of Clinical Microbiology, September 1998, p. 2640-2644, Vol. 36, No. 9
Division of Experimental Pathology and
Clinical Microbiology, Department of Laboratory Medicine and Pathology,
Mayo Clinic and Foundation, Rochester,
Minnesota1;
Chiron Diagnostics, East
Walpole, Massachusetts2; and
Chiron
Diagnostics, Emeryville, California3
Received 26 March 1998/Returned for modification 28 April
1998/Accepted 11 June 1998
The identification of methicillin-resistant staphylococcus isolates
in the clinical laboratory has typically been performed by using
methods that detect phenotypic expression of resistance determinants.
However, these methods may be difficult to interpret and some isolates
do not express resistance until selective pressure is administered.
Assays that detect genetic determinants are not subject to these
limitations and have been effective in distinguishing isolates that are
capable of expressing the resistance phenotype. In this study, a novel
branched-DNA (bDNA) hybridization assay was used to test for the
mecA gene in 416 clinical staphylococcal isolates. The
results were compared with those obtained by a PCR-based assay and
oxacillin disk diffusion. For 155 Staphylococcus aureus and
261 coagulase-negative Staphylococcus isolates, the bDNA
assay and PCR results were 100% concordant. Among the S. aureus isolates, 20 were MecA+ and 135 were
MecA
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Branched-DNA Assay for Detection of the
mecA Gene in Oxacillin-Resistant and
Oxacillin-Sensitive Staphylococci
. For the coagulase-negative staphylococci, 150 were
MecA+ and 111 were MecA
. The results from the
genotypic detection methods were compared with those obtained by
oxacillin disk diffusion. No discrepancies were detected among the
S. aureus isolates; however, 10 coagulase-negative isolates
were MecA+ but oxacillin sensitive and 1 isolate was
MecA
but oxacillin resistant. Oxacillin resistance was
induced in 6 of the 10 MecA+ isolates previously classified
as oxacillin sensitive. These results suggest that the bDNA method
described here is a sensitive and efficient method for detection of
methicillin resistance in staphylococci and that genetic detection
methods may be useful for detection of potential methicillin resistance
in the clinical laboratory.
*
Corresponding author. Mailing address: Division of
Experimental Pathology and Clinical Microbiology, Dept. of Laboratory
Medicine and Pathology, Mayo Clinic and Foundation, 200 First St.
Southwest, Rochester, MN 55905. Phone: (507) 284-2511. Fax: (507)
284-3757. E-mail: Persing.David{at}mayo.edu.
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