Rapid detection of mecA-positive and mecA-negative coagulase-negative staphylococci by an anti-penicillin binding protein 2a slide latex agglutination test
Z. Hussain et al., Rapid detection of mecA-positive and mecA-negative coagulase-negative staphylococci by an anti-penicillin binding protein 2a slide latex agglutination test, J CLIN MICR, 38(6), 2000, pp. 2051-2054
A rapid slide latex agglutination (LA) test, MRSA-Screen (Denka Seiken Co.,
Niigata, Japan), which detects PBP 2a, was tested for its ability to diffe
rentiate between mecA-positive and -negative coagulase-negative staphylococ
ci. A total of 463 isolates from 13 species were included in the study. The
mecA gene was detected by PCR, and the oxacillin MIC was determined by the
agar dilution method according to the guidelines of the National Committee
for Clinical Laboratory Standards (NCCLS), The LA test was performed with
oxacillin-induced isolates, The true-positive and true-negative results wer
e defined on the basis of the presence or the absence of the mecA gene. By
PCR, 251 isolates were mecA positive and 212 were mecA negative. The sensit
ivities, specificities, and positive and negative predictive values for the
LA test compared to the NCCLS breakpoint for oxacillin resistance (greater
than or equal to 0.5 mg/liter) were as follows: for the LA test, 100, 99.5
, 99.6, and 100%, respectively; for the NCCLS breakpoint, 100, 60.8, 75.1,
and 100%, respectively. One hundred twenty-five mecA-positive isolates were
also tested by the LA test without induction of PBP 2a; only 72 (57.6%) ga
ve a positive result and required 3 to 15 min for reaction. With induction,
all 251 isolates were positive within 3 min. The LA test was reliable in c
lassifying mecA-negative isolates, but it classified isolates for which the
oxacillin MIC was greater than or equal to 0.5 mg/liter as oxacillin susce
ptible. For the reliable detection of oxacillin resistance by the MRSA-Scre
en in coagulase-negative staphylococci, induction of the mecA gene appears
to be necessary.