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Journal of Clinical Microbiology, December 1999, p. 4192-4193, Vol. 37, No. 12
Division of Clinical Microbiology, Department
of Laboratory Medicine and Pathology, Mayo Clinic and Foundation,
Rochester, Minnesota1; Bayer
Diagnostics, East Walpole, Massachusetts2;
and Bayer Diagnostics, Emeryville, California3
Received 26 May 1999/Returned for modification 28 June
1999/Accepted 23 August 1999
A branched-DNA (bDNA) signal amplification method was used to
detect the mecA gene directly from blood culture broth
growing staphylococci. BACTEC blood culture bottles with positive
growth indices and containing staphylococcus-like organisms as shown by
Gram stain were tested for the presence of the mecA gene.
Comparison of test results was done among 225 patients (one blood
culture from each patient). Compared with PCR, the sensitivity and
specificity of the bDNA method are 100 and 99%, respectively. The bDNA
test is carried out in a 96-well format and requires approximately 6 h to perform. Our preliminary results suggest that direct
detection of the mecA gene by bDNA signal amplification is
(i) sensitive enough to detect mecA directly from blood
culture bottles without the requirement for subculture and (ii) as
sensitive and specific as the PCR-based method.
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Direct mecA Detection from Blood Culture
Bottles by Branched-DNA Signal Amplification

*
Corresponding author. Present address: Corixa
Corporation and Infectious Disease Research Institute, Seattle Life
Sciences Center, Suite 200, 1124 Columbia St., Seattle, WA 98104. Phone: (206) 754-5879. Fax: (206) 754-5715. E-mail:
Persing{at}corixa.com.
Present address: Department of Microbiology, Diagnostic Laboratory
Services, The Queen's Medical Center, Honolulu, HI 96813.
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