During two clinical trials involving the treatment of 835 out patients with
infected diabetic foot ulcers, 2515 bacterial isolates, including 2337 aer
obes and 178 anaerobes, were grown from cultures of the ulcers. The in vitr
o susceptibility of these isolates was determined to pexiganan, a peptide a
nti-infective evaluated in these clinical trials, and to other classes of a
ntibiotics. Pexiganan demonstrated broad spectrum antimicrobial activity ag
ainst Gram-positive and Guam-negative aerobes and anaerobes. The MIC90 valu
es for the most common species among 1735 Gram-positive aerobes isolated, s
uch as Staphylococcus aureus, coagulase-negative staphylococci, Group A str
eptococci, and Group B streptococci, were 16 mu g/mL or less. Of 602 Gram-n
egative aerobes tested, the MIC90 values for pexiganan were 16 mu g/mL ou l
ess for Acinetobacter, Pseudomonas, Stenotrophomonas, Citrobacter, Enteroba
cter, Escherichia, Klebsiella, and Flavobacterium species. Pexiganan had a
MIC90 of 4 to 16 mu g/mL against the anaerobic isolates of Bacteroides, Pep
tostreptococcus, Clostridium, and Prevotella species. Importantly pexiganan
did not exhibit cross-resistance with other commonly used antibiotics, inc
luding beta-lactams, quinolones, macrolides, and lincosamides. The broad sp
ectrum in vitro antimicrobial activity of pexiganan against clinical isolat
es from infected diabetic foot ulcers supports its potential as a local the
rapy for infected diabetic foot ulcers. (C) 1999 Elsevier Science Inc.