K. Sieradzki et al., DECREASED SUSCEPTIBILITIES TO TEICOPLANIN AND VANCOMYCIN AMONG COAGULASE-NEGATIVE METHICILLIN-RESISTANT CLINICAL ISOLATES OF STAPHYLOCOCCI, Antimicrobial agents and chemotherapy, 42(1), 1998, pp. 100-107
Of 41 methicillin-resistant coagulase-negative staphylococcal clinical
isolates collected during a 5-month period between late 1995 and earl
y 1996, 28 showed tube dilution teicoplanin MICs of 4 to 8 mu g/ml whi
ch increased to 16 to 32 mu g/ml upon prolonged incubation, Cultures o
f such bacteria were heterogeneous; they contained subpopulations with
frequencies of 10(-5) to 10(-4) that could grow on up to 50 mu g of t
eicoplanin per mi, The same cultures were also heterogeneous with resp
ect to susceptibility to vancomycin; while the MICs for the majority o
f cells were 2 to 4 mu g/ml, subpopulations that could grow on 6 to 12
mu g of vancomycin per mi were also present at frequencies of 10(-5)
to 10(-7). Selective enrichment of such cultures for the resistant sub
population occurred with relative ease under laboratory conditions, He
terogeneous phenotypes for teicoplanin (but not for vancomycin) suscep
tibility were also identified in several Staphylococcus epidermidis is
olates collected during the preantibiotic era, The addition of half th
e MIC of teicoplanin inhibited autolysis and caused formation of cellu
lar aggregates which disintegrated to individual bacteria in the stati
onary phase when the titer of teicoplanin in the medium fell to undete
ctable levels, indicating removal of the antibiotic from the culture m
edium by the bacteria.