R. Pajukanta et al., BETA-LACTAMASE PRODUCTION AND INVITRO ANTIMICROBIAL SUSCEPTIBILITY OFPORPHYROMONAS-GINGIVALIS, FEMS immunology and medical microbiology, 6(2-3), 1993, pp. 241-244
Beta-lactamase production by 98 Porphyromonas strains was investigated
by the nitrocefin (chromogenic cephalosporin) test. Human isolates of
P. gingivalis (91), P. endodontalis (2), and P. asaccharolytica (1) w
ere tested, with four closely related Porphyromonas spp. of animal ori
gin and four reference strains. The in vitro susceptibility of 64 P. g
ingivalis strains was investigated on Brucella blood agar by the E tes
t. None of the human Porphyromonas isolates tested produced beta-lacta
mase, but one Porphyromonas strain of animal origin, most closely rese
mbling P. endodontalis, produced beta-lactamase. P. gingivalis was sus
ceptible to almost all of the drugs tested: benzylpenicillin, ampicill
in, cefaclor, cefuroxime, erythromycin, clindamycin, tetracycline, dox
ycycline, metronidazole and ciprofloxacin; all strains were inhibited
at 0.016 mug/ml, 0.023 mug/ml, 0.315 mug/ml, 0.064 mug/ml, 0.19 mug/ml
, 0.016 mug/ml, 0.094 mug/ml, 0.047 mug/ml, 0.023 mug/ml, and 0.75 mug
/ml of these drugs, respectively. Cotrimoxazole exhibited variable eff
icacy against P. gingivalis; the range of MICs was 0.1095-32.0 mug/ml.
The results indicate that beta-lactamase production is currently not
a problem amongst clinical isolates of P. gingivalis and strains are s
usceptible to most antimicrobial agents.