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The MUT056399 Inhibitor of FabI is a New Antistaphylococcal Compound

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Specialty Pharmacology
Date 2011 Aug 10
PMID 21825292
Citations 41
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Abstract

MUT056399 is a highly potent new inhibitor of the FabI enzyme of both Staphylococcus aureus and Escherichia coli. In vitro, MUT056399 was very active against S. aureus strains, including methicillin-susceptible S. aureus (MSSA), methicillin-resistant S. aureus (MRSA), linezolid-resistant, and multidrug-resistant strains, with MIC(90)s between 0.03 and 0.12 μg/ml. MUT056399 was also active against coagulase-negative staphylococci, with MIC(90)s between 0.12 and 4 μg/ml. The antibacterial spectrum is consistent with specific FabI inhibition with no activity against bacteria using FabK but activity against FabI-containing Gram-negative bacilli. In vitro, resistant clones of S. aureus were obtained at a low frequency. All of the resistant clones analyzed were found to contain mutations in the fabI gene. In vivo, MUT056399, administered subcutaneously, protected mice from a lethal systemic infection induced by MSSA, MRSA, and vancomycin-intermediate S. aureus strains (50% effective doses ranging from 19.3 mg/kg/day to 49.6 mg/kg/day). In the nonneutropenic murine thigh infection model, the same treatment with MUT056399 reduced the bacterial multiplication of MSSA and MRSA in the thighs of immunocompetent mice. These properties support MUT056399 as a very promising candidate for a novel drug to treat severe staphylococcal infections.

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References
1.
Balemans W, Lounis N, Gilissen R, Guillemont J, Simmen K, Andries K . Essentiality of FASII pathway for Staphylococcus aureus. Nature. 2010; 463(7279):E3. DOI: 10.1038/nature08667. View

2.
Zhang Y, White S, Rock C . Inhibiting bacterial fatty acid synthesis. J Biol Chem. 2006; 281(26):17541-4. DOI: 10.1074/jbc.R600004200. View

3.
Xu H, Sullivan T, Sekiguchi J, Kirikae T, Ojima I, Stratton C . Mechanism and inhibition of saFabI, the enoyl reductase from Staphylococcus aureus. Biochemistry. 2008; 47(14):4228-36. PMC: 4397500. DOI: 10.1021/bi800023a. View

4.
Heath R, White S, Rock C . Inhibitors of fatty acid synthesis as antimicrobial chemotherapeutics. Appl Microbiol Biotechnol. 2002; 58(6):695-703. DOI: 10.1007/s00253-001-0918-z. View

5.
Ling L, Xian J, Ali S, Geng B, Fan J, Mills D . Identification and characterization of inhibitors of bacterial enoyl-acyl carrier protein reductase. Antimicrob Agents Chemother. 2004; 48(5):1541-7. PMC: 400533. DOI: 10.1128/AAC.48.5.1541-1547.2004. View