In vitro activity of rifampicin, rifapentine and rifabutin in combination with their 25-deacetyl-metabolites against various Mycobacterium tuberculosis lineages.

IF 4.6 2区 医学 Q1 MICROBIOLOGY
Charlotte Genestet, Chloé Bourg, Elisabeth Hodille, Olivier Bahuaud, Florence Ader, Sylvain Goutelle, Oana Dumitrescu
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引用次数: 0

Abstract

Objectives: Rifamycin agents (rifampicin (RIF), rifapentine (RFP), rifabutin (RFB)) are the cornerstone of tuberculosis (TB) therapy. Rifamycins are metabolized into 25-deacetyl-metabolites, which have been described has active and may contribute to in vivo drug effect. However, little is known about the combined effect of rifamycins and their metabolites across different Mycobacterium tuberculosis complex (MTBC) lineages.

Methods: This study included 14 MTBC strains representing the main lineages. Minimum inhibitory concentrations (MICs) were determined using microdilution assays for the three rifamycins and their metabolites. A checkerboard assay was used to assess drug interactions, with the fractional inhibitory concentration (FIC) index calculated for synergy or antagonism.

Results: MICs varied across rifamycins, RIF and its metabolite showed the highest MICs, followed by RFP and RFB and their respective metabolites. FIC indices for rifamycin-metabolite combinations indicated additive effects (FIC between 0.5 and 1.25), with no antagonism observed, even at clinically relevant metabolite-to-parent drug ratios, and without impact of MTBC lineage.

Conclusions: Rifamycin metabolites exhibit additive effects with parent drugs, potentially enhancing bactericidal activity. This highlights that rifamycin susceptibility testing should account for both parent drugs and their metabolites, as these metabolites also exhibit antimicrobial activity. Additionally, these findings support further pharmacokinetic/pharmacodynamic studies to optimize TB treatment regimens, particularly in relation to metabolite-to-parent drug ratios in patients.

利福平、利福喷丁和利福布汀联合其25-去乙酰代谢物对多种结核分枝杆菌的体外活性研究
目的:利福霉素类药物(利福平(RIF)、利福喷丁(RFP)、利福布汀(RFB))是结核病(TB)治疗的基石。利福霉素被代谢为25-去乙酰代谢物,已被描述为具有活性并可能有助于体内药物效应。然而,关于利福霉素及其代谢物在不同结核分枝杆菌复合体(MTBC)谱系中的联合作用知之甚少。方法:选取代表主要谱系的14株MTBC菌株。采用微量稀释法测定三种利福霉素及其代谢物的最低抑菌浓度(mic)。棋盘法用于评估药物相互作用,用分数抑制浓度(FIC)指数计算协同作用或拮抗作用。结果:不同利福霉素的mic差异较大,RIF及其代谢物mic最高,RFP和RFB及其代谢物mic次之。利福霉素-代谢物组合的FIC指数显示了累加效应(FIC在0.5和1.25之间),即使在临床相关的代谢物与亲本药物比率下,也没有观察到拮抗作用,并且对MTBC谱系没有影响。结论:利福霉素代谢物与母体药物表现出加性作用,可能增强抗菌活性。这突出表明,利福霉素药敏试验应考虑母体药物及其代谢物,因为这些代谢物也表现出抗菌活性。此外,这些发现支持进一步的药代动力学/药效学研究,以优化结核病治疗方案,特别是与患者的代谢物与母体药物比率有关。
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来源期刊
CiteScore
8.60
自引率
0.00%
发文量
49
审稿时长
>12 weeks
期刊介绍: Annals of Clinical Microbiology and Antimicrobials considers good quality, novel and international research of more than regional relevance. Research must include epidemiological and/or clinical information about isolates, and the journal covers the clinical microbiology of bacteria, viruses and fungi, as well as antimicrobial treatment of infectious diseases. Annals of Clinical Microbiology and Antimicrobials is an open access, peer-reviewed journal focusing on information concerning clinical microbiology, infectious diseases and antimicrobials. The management of infectious disease is dependent on correct diagnosis and appropriate antimicrobial treatment, and with this in mind, the journal aims to improve the communication between laboratory and clinical science in the field of clinical microbiology and antimicrobial treatment. Furthermore, the journal has no restrictions on space or access; this ensures that the journal can reach the widest possible audience.
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