In vitro susceptibility to pexiganan of bacteria isolated from infected diabetic foot ulcers

被引:83
作者
Ge, YG [1 ]
MacDonald, D
Henry, MM
Halt, HI
Nelson, KA
Lipsky, BA
Zasloff, MA
Holroyd, KJ
机构
[1] Magainin Pharmaceut Inc, Dept Microbiol, Plymouth Meeting, PA 19462 USA
[2] Covance Cent Lab Serv Inc, Indianapolis, IN USA
[3] Univ Washington, Sch Med, Dept Med, Seattle, WA 98195 USA
[4] VA Puget Sound Hlth Care Syst, Med Serv, Seattle, WA USA
关键词
D O I
10.1016/S0732-8893(99)00056-5
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
During two clinical trials involving the treatment of 835 out patients with infected diabetic foot ulcers, 2515 bacterial isolates, including 2337 aerobes and 178 anaerobes, were grown from cultures of the ulcers. The in vitro susceptibility of these isolates was determined to pexiganan, a peptide anti-infective evaluated in these clinical trials, and to other classes of antibiotics. Pexiganan demonstrated broad spectrum antimicrobial activity against Gram-positive and Guam-negative aerobes and anaerobes. The MIC90 values for the most common species among 1735 Gram-positive aerobes isolated, such as Staphylococcus aureus, coagulase-negative staphylococci, Group A streptococci, and Group B streptococci, were 16 mu g/mL or less. Of 602 Gram-negative aerobes tested, the MIC90 values for pexiganan were 16 mu g/mL ou less for Acinetobacter, Pseudomonas, Stenotrophomonas, Citrobacter, Enterobacter, Escherichia, Klebsiella, and Flavobacterium species. Pexiganan had a MIC90 of 4 to 16 mu g/mL against the anaerobic isolates of Bacteroides, Peptostreptococcus, Clostridium, and Prevotella species. Importantly pexiganan did not exhibit cross-resistance with other commonly used antibiotics, including beta-lactams, quinolones, macrolides, and lincosamides. The broad spectrum in vitro antimicrobial activity of pexiganan against clinical isolates from infected diabetic foot ulcers supports its potential as a local therapy for infected diabetic foot ulcers. (C) 1999 Elsevier Science Inc.
引用
收藏
页码:45 / 53
页数:9
相关论文
共 19 条
[1]  
BOMAN HG, 1995, ANNU REV IMMUNOL, V13, P61, DOI 10.1146/annurev.iy.13.040195.000425
[2]   In vitro antimicrobial activity of MSI-78, a magainin analog [J].
Fuchs, PC ;
Barry, AL ;
Brown, SD .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (05) :1213-1216
[3]   In vitro antibacterial properties of pexiganan, an analog of magainin [J].
Ge, YG ;
MacDonald, DL ;
Holroyd, KJ ;
Thornsberry, C ;
Wexler, H ;
Zasloff, M .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (04) :782-788
[4]   USE OF AMPICILLIN/SULBACTAM VERSUS IMIPENEM/CILASTATIN IN THE TREATMENT OF LIMB-THREATENING FOOT INFECTIONS IN DIABETIC-PATIENTS [J].
GRAYSON, ML ;
GIBBONS, GW ;
HABERSHAW, GM ;
FREEMAN, DV ;
POMPOSELLI, FB ;
ROSENBLUM, BI ;
LEVIN, E ;
KARCHMER, AW .
CLINICAL INFECTIOUS DISEASES, 1994, 18 (05) :683-693
[5]   Peptide antibiotics [J].
Hancock, REW .
LANCET, 1997, 349 (9049) :418-422
[6]  
Holzer SES, 1998, CLIN THER, V20, P169
[7]  
JACOB L, 1994, CIBA F SYMP, V186, P197
[8]  
Levin M, 1997, Adv Wound Care, V10, P24
[9]   OUTPATIENT MANAGEMENT OF UNCOMPLICATED LOWER-EXTREMITY INFECTIONS IN DIABETIC-PATIENTS [J].
LIPSKY, BA ;
PECORARO, RE ;
LARSON, SA ;
HANLEY, ME ;
AHRONI, JH .
ARCHIVES OF INTERNAL MEDICINE, 1990, 150 (04) :790-797
[10]  
LIPSKY BA, 1997, 37 INT C ANT AG CHEM, V74