Contezolid can replace linezolid in a novel combination with bedaquiline and pretomanid in a murine model of tuberculosis

被引:3
|
作者
Almeida, Deepak [1 ]
Li, Si-Yang [1 ]
Lee, Jin [1 ]
Hafkin, Barry [2 ]
Mdluli, Khisimuzi [3 ]
Fotouhi, Nader [3 ]
Nuermberger, Eric L. [1 ]
机构
[1] Johns Hopkins Univ, Ctr TB Res, Dept Med, Baltimore, MD 21218 USA
[2] MicuRx Pharmaceut, Foster City, CA USA
[3] Global Alliance TB Drug Dev, New York, NY USA
关键词
contezolid; Mycobacterium tuberculosis; oxazolidinones; MYCOBACTERIUM-TUBERCULOSIS; NITROIMIDAZOPYRAN PA-824; REDUCED SUSCEPTIBILITY; REGIMENS; MUTATIONS; EFFICACY; SAFETY; DRUGS;
D O I
10.1128/aac.00789-23
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Contezolid is a new oxazolidinone with in vitro and in vivo activity against Mycobacterium tuberculosis comparable to that of linezolid. Pre-clinical and clinical safety studies suggest it may be less toxic than linezolid, making contezolid a potential candidate to replace linezolid in the treatment of drug-resistant tuberculosis. We evaluated the dose-ranging activity of contezolid, alone and in combination with bedaquiline and pretomanid, and compared it with linezolid at similar doses, in an established BALB/c mouse model of tuberculosis. Contezolid had an MIC of 1 mu g/mL, similar to linezolid, and exhibited similar bactericidal activity in mice. Contezolid-resistant mutants selected in vitro had 32- to 64-fold increases in contezolid MIC and harbored mutations in the mce3R gene. These mutants did not display cross-resistance to linezolid. Our results indicate that contezolid has the potential to replace linezolid in regimens containing bedaquiline and pretomanid and likely other regimens.
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页数:7
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