N. Kobayashi et al., DETECTION OF MECA, FEMA, AND FEMB GENES IN CLINICAL STRAINS OF STAPHYLOCOCCI USING POLYMERASE CHAIN-REACTION, Epidemiology and infection, 113(2), 1994, pp. 259-266
MecA, a structural gene located on the chromosome of Staphylococcus au
reus, characterizes methicillin-resistant S. aureus (MRSA), and femA a
nd femB(fem) genes encode proteins which influence the level of methic
illin resistance of S. aureus. In order to examine effectiveness of de
tecting mecA and fern genes in identification of MRSA, the presence of
these genes in 237 clinically isolated strains of staphylococci was i
nvestigated by polymerase chain reaction (PCR). An amplified mecA DNA
fragment of 533 base pairs (bp) was detected in 100% of oxacillin-resi
stant S. aureus, in 16.7% of oxacillin-sensitive S. aureus, in 81.5% o
f S. epidermidis, and in 58.3% of other coagulase-negative staphylococ
ci (CNS). While the PCR product of femA (509 bp) or femB (651 bp) was
obtained from almost all the S. aureus strains except for five oxacill
in-resistant strains (2.5%), neither of these genes were detected in C
NS. Therefore, the detection of femA and femB together with mecA by PC
R was considered to be a more reliable indicator to identify MRSA by d
ifferentiating it from mecA-positive CNS than single detection of mecA
.