Citation
M. Tanaka et al., ANTIMICROBIAL ACTIVITY OF DV-7751A, A NEW FLUOROQUINOLONE, Antimicrobial agents and chemotherapy, 37(10), 1993, pp. 2112-2118
Abstract
We compared the in vitro antibacterial activity of DV-7751a against gr
am-positive and -negative bacteria with those of quinolones currently
available. MICs for 90% of the strains tested (MIC90s) against clinica
l isolates of methicillin-susceptible and -resistant Staphylococcus au
reus and Staphylococcus epidermidis were 0.20, 0.39, 0.20, and 0.78 mu
g/ml, respectively. Moreover, MIC50s for DV-7751a against ofloxacin-re
sistant methicillin-resistant S. aureus were 4-, 8-, 16-, 32-, and 64-
fold lower than those for tosufloxacin and sparfloxacin, levofloxacin,
ofloxacin and fleroxacin, ciprofloxacin, and lomefloxacin, respective
ly. DV-7751a inhibited the growth of all strains of Streptococcus pneu
moniae, Streptococcus pyogenes, and Peptostreptococcus spp. at 0.39, 0
.39, and 0.78 mug/ml, respectively, and was 4- to > 16-fold more activ
e against enterococci at the MIC90 level than the other quinolones tes
ted. The activity of DV-7751a against Pseudomonas aeruginosa was rough
ly comparable to those of levofloxacin and sparfloxacin at the MIC90 l
evel and was two- to fourfold less than that of ciprofloxacin. DV-7751
a showed activity comparable to those of levofloxacin and ciprofloxaci
n against the other glucose-nonfermenting bacteria Haemophilus influen
zae, Neisseria gonorrhoeae, and Moraxella catarrhalis (MIC90s of 0.025
, 0.20, and 0.10 mug/ml, respectively). DV-7751a activity was not affe
cted by medium, inoculum size, or the addition of human serum but was
decreased under acidic conditions and in human urine, as were the othe
r quinolones tested. Time-kill curve studies demonstrated the rapid ba
ctericidal action of DV-7751a against S. aureus, S. pneumoniae, Escher
ichia coli, and P. aeruginosa. The frequency of spontaneous resistance
to DV-7751a was less than or equal to those of the reference drugs. D
V-7751a inhibited the supercoiling activity of DNA gyrases from S. aur
eus, E. coli, and P. aeruginosa at concentrations comparable to those
of levofloxacin and sparfloxacin.