A carbon monoxide-releasing molecule (CORM-3) exerts bactericidal activity against Pseudomonas aeruginosa and improves survival in an animal model of bacteraemia

被引:135
作者
Desmard, Mathieu [1 ,2 ,6 ]
Davidge, Kelly S. [3 ]
Bouvet, Odile
Morin, Didier [4 ]
Roux, Damien
Foresti, Roberta [8 ,9 ]
Ricard, Jean D. [5 ]
Denamur, Erick
Poole, Robert K. [3 ]
Montravers, Philippe [6 ]
Motterlini, Roberto [8 ,9 ]
Boczkowski, Jorge [1 ,2 ,7 ]
机构
[1] Univ Paris 07, Fac Med, INSERM, U700, Paris, France
[2] Univ Paris 07, Fac Med, INSERM, U722, Paris, France
[3] Univ Sheffield, Dept Mol Biol & Biotechnol, Western Bank, Sheffield S10 2TN, S Yorkshire, England
[4] Univ Paris 12, Fac Med, INSERM, U841 Equipe 3, Creteil, France
[5] Hop Louis Mourier, AP HP, F-92701 Colombes, France
[6] Hop Bichat Claude Bernard, AP HP, Dept Anesthesie Reanimat Chirurg, F-75877 Paris 18, France
[7] Hop Bichat Claude Bernard, AP HP, Ctr Invest Clin 07, F-75877 Paris 18, France
[8] Northwick Pk Inst Med Res, Dept Surg Res, Harrow, Middx, England
[9] Italian Inst Technol, Dept Drug Discovery & Dev, Genoa, Italy
基金
英国生物技术与生命科学研究理事会;
关键词
pharmacology; anti-infective agents; sepsis; microbiology; THERAPEUTIC APPLICATIONS; MITOCHONDRIAL; CO; SENSITIVITY; INFECTIONS; OXIDASE; TARGETS;
D O I
10.1096/fj.08-122804
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The search for new molecules to fight Pseudomonas aeruginosa is of paramount importance. Carbon monoxide (CO) is known to act as an effective inhibitor of the respiratory chain in P. aeruginosa, but the practical use of this gas as an antibacterial molecule is hampered by its toxicity and difficulty to manipulate. Here, we show that a water-soluble CO releaser (CORM-3) possesses bactericidal properties against laboratory and antibiotic-resistant P. aeruginosa. CORM-3 reduced the bacterial count by 4 logs 180 min after in vitro treatment. CORM-3-treated bacteria had a lower O-2 consumption than vehicle-treated bacteria, and the decrease in O-2 consumption temporally preceded the bactericidal action of CORM-3. These results support the hypothesis that the antimicrobial effect of CORM-3 is mediated by an interaction of CO liberated by the carrier with the bacterial respiratory chain. The antibacterial effect occurred at concentrations of CORM-3 that are 50-fold lower than toxic concentrations for eukaryotic cells. CORM-3 treatment compared to vehicle treatment decreased bacterial counts in the spleen and increased survival in immunocompetent and immunosuppressed mice following P. aeruginosa bacteremia. Our results suggest that CORMs could form the basis for developing a new therapeutic strategy against P. aeruginosa-induced infection.-Desmard, M., Davidge, K. S., Bouvet, O., Morin, D., Roux, D., Foresti, R., Ricard, J. D., Denamur, E., Poole, R. K., Montravers, P., Motterlini, R., Boczkowski, J. A carbon monoxide-releasing molecule (CORM-3) exerts bactericidal activity against Pseudomonas aeruginosa and improves survival in an animal model of bacteraemia. FASEB J. 23, 1023-1031 (2009)
引用
收藏
页码:1023 / 1031
页数:9
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