Detection of methicillin-resistant Staphylococcus aureus (MRSA) from growth on mannitol salt oxacillin agar using PCR for nosocomial surveillance

Citation
P. Jayaratne et C. Rutherford, Detection of methicillin-resistant Staphylococcus aureus (MRSA) from growth on mannitol salt oxacillin agar using PCR for nosocomial surveillance, DIAG MICR I, 35(1), 1999, pp. 13-18
Citations number
14
Categorie Soggetti
Clinical Immunolgy & Infectious Disease",Microbiology
Journal title
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE
ISSN journal
07328893 → ACNP
Volume
35
Issue
1
Year of publication
1999
Pages
13 - 18
Database
ISI
SICI code
0732-8893(199909)35:1<13:DOMSA(>2.0.ZU;2-9
Abstract
This study evaluated a polymerase chain reaction (PCR) method for detection of methicillin-resistant Staphylococcus aureus (MRSA) in specimens referre d for nosocomial surveillance. PCR was used to detect the mecA and nuc gene targets using yellow growth on mannitol salt agar containing 6 mg/liter ox acillin (MSO-6) as a source of DNA (N = 645). The diagnostic values for PCR compared with culture methods were 97% specificity, 100% sensitivity, 96% positive predictive value, and 100% negative predictive value. Total cost f or PCR per test is $3.62 compared to $4.77 for culture. However, the fetal cost per specimen is significantly lower due to only 20% of all surveillanc e specimens producing yellow colonies on MSO-6. The average turnaround time for the PCR method is 48 h compared with 82 h for culture. PCR an amplific ation of mecA and nuc genes using yellow colonies on MSO-6 is a simple, fas t, accurate and cost-effective method for routine use in clinical laborator ies ies for detecting MRSA in surveillance specimens. (C) 1999 Elsevier Sci ence Inc.