In vitro antibacterial activity of aminosterols against multidrug-resistant bacteria from patients with cystic fibrosis

被引:19
作者
Alhanout, Kamel [1 ]
Brunel, Jean-Michel [1 ]
Raoult, Didier [1 ]
Rolain, Jean-Marc [1 ]
机构
[1] Fac Med & Pharm, CNRS IRD, URMITE UMR 6236, F-13385 Marseille 05, France
关键词
squalamine; antibiotics; infections; SQUALAMINE;
D O I
10.1093/jac/dkp281
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: Respiratory infections with multidrug-resistant (MDR) bacteria are life-threatening in patients with cystic fibrosis (CF). Squalamine and aminosterol derivatives (ASDs) have previously demonstrated interesting antibacterial activity against bacterial reference strains. This study investigated for the first time their activity against MDR clinical isolates recovered from the sputa of CF patients. Methods: Antibacterial activity of squalamine and two ASDs (1 and 2) was evaluated against 135 MDR Gram-negative and Gram-positive bacteria using the broth microdilution method for MIC determination. Results: For Gram-negative bacteria, MICs ranged from 2 to 128 mg/L. Resistance to colistin and mucoidity were significantly associated with higher MICs of squalamine and ASDs 1 and 2. Tested compounds were active against various Gram-positive bacteria with MIC values varying from 0.5 to 8 mg/L, with the exception of two capsulated isolates of Streptococcus pneumoniae demonstrating MICs of 32 mg/L. Conclusions: In this study, we present new findings concerning the antibacterial potential of ASDs against MDR bacteria. Colistin-resistant, mucoid and capsulated bacteria were found to exhibit decreased susceptibility to ASDs indicating that these compounds might share some mechanistic aspects with polymyxins towards Gram-negative bacteria. However, ASDs were remarkably active against Gram-positive species suggesting different mechanisms of action towards Gram-positive and Gram-negative bacteria. As tested ASDs exhibited elevated MiCs in some cases, we believe that these compounds may be developed to be locally administrated as aerosols rather than via systemic administration routes. Further work is warranted to evaluate their in vivo efficacy in aerosol formulations using a lung-infected animal model.
引用
收藏
页码:810 / 814
页数:5
相关论文
共 10 条
[1]   The rpoB gene as a tool for clinical microbiologists [J].
Adekambi, Toidi ;
Drancourt, Michel ;
Raoult, Didier .
TRENDS IN MICROBIOLOGY, 2009, 17 (01) :37-45
[2]   Determination of minimum inhibitory concentrations [J].
Andrews, JM .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2001, 48 :5-16
[3]   Bugs, Biofilms, and Resistance in Cystic Fibrosis [J].
Davies, Jane C. ;
Bilton, Diana .
RESPIRATORY CARE, 2009, 54 (05) :628-638
[4]  
Herbst RS, 2003, CLIN CANCER RES, V9, P4108
[5]   Evaluation of colistin as an agent against multi-resistant in Gram-negative bacteria [J].
Li, J ;
Nation, RL ;
Milne, RW ;
Turnidge, JD ;
Coulthard, K .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2005, 25 (01) :11-25
[6]   Capsule polysaccharide is a bacterial decoy for antimicrobial peptides [J].
Llobet, Enrique ;
Tomas, Juan M. ;
Bengoechea, Jose A. .
MICROBIOLOGY-SGM, 2008, 154 :3877-3886
[7]   New stereoselective titanium reductive amination synthesis of 3-amino and polyaminosterol derivatives possessing antimicrobial activities [J].
Salmi, Chanaz ;
Loncle, Celine ;
Vidal, Nicolas ;
Letourneux, Yves ;
Brunel, Jean Michel .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2008, 43 (03) :540-547
[8]   Therapeutic potential of cationic steroid antibacterials [J].
Salmi, Chanaz ;
Brunel, Jean M. .
EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2007, 16 (08) :1143-1157
[9]   Squalamine: An Appropriate Strategy against the Emergence of Multidrug Resistant Gram-Negative Bacteria? [J].
Salmi, Chanaz ;
Loncle, Celine ;
Vidal, Nicolas ;
Letourneux, Yves ;
Fantini, Jacques ;
Maresca, Marc ;
Taieb, Nadira ;
Pages, Jean-Marie ;
Brunel, Jean Michel .
PLOS ONE, 2008, 3 (07)
[10]  
TOUW DJ, 1995, EUR RESPIR J, V8, P1594