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比阿培南对药物敏感和耐利福平结核分枝杆菌的体外及体内活性

In vitro and in vivo activity of biapenem against drug-susceptible and rifampicin-resistant Mycobacterium tuberculosis.

作者信息

Kaushik Amit, Ammerman Nicole C, Tasneen Rokeya, Story-Roller Elizabeth, Dooley Kelly E, Dorman Susan E, Nuermberger Eric L, Lamichhane Gyanu

机构信息

Center for Tuberculosis Research, Johns Hopkins University School of Medicine, 1550 Orleans Street, Baltimore, MD 21287, USA.

出版信息

J Antimicrob Chemother. 2017 Aug 1;72(8):2320-2325. doi: 10.1093/jac/dkx152.

Abstract

BACKGROUND

Biapenem, a carbapenem antibiotic, has been shown to have synergistic bactericidal anti-TB activity when combined with rifampicin both in vitro and in the mouse model of TB chemotherapy. We hypothesized that this synergy would result in biapenem/rifampicin activity against rifampicin-resistant Mycobacterium tuberculosis .

OBJECTIVES

Our objective was to evaluate the synergy of biapenem/rifampicin against both low- and high-level rifampicin-resistant strains of M. tuberculosis , in vitro and in the mouse model.

METHODS

Biapenem/rifampicin activity was evaluated using three strains of M. tuberculosis : strain 115R (low-level rifampicin resistance); strain 124R (high-level rifampicin resistance); and the drug-susceptible H37Rv parent strain. Biapenem/rifampicin synergy was evaluated in vitro by chequerboard titration. In vivo , we first conducted a dose-ranging experiment with biapenem against H37Rv in the mouse model. We then evaluated biapenem/rifampicin activity in mice infected with each M. tuberculosis strain.

RESULTS

In vitro , synergy was observed between biapenem and rifampicin against H37Rv and strain 115R. In vivo , biapenem exhibited clear dose-dependent activity against H37Rv, with all biapenem doses as active or more active than rifampicin alone. Biapenem and rifampicin had synergistic bactericidal activity against H37Rv in the mouse model; no synergy was observed in mice infected with either of the rifampicin-resistant strains. Biapenem alone was active against all three strains.

CONCLUSIONS

Our preclinical experiments indicate that biapenem has potential for use as an anti-TB drug, including for use against rifampicin-resistant TB. Thus, biapenem has promise for repurposing as a 'new' - and desperately needed - drug for the treatment of drug-resistant TB.

摘要

背景

比阿培南是一种碳青霉烯类抗生素,在体外和结核病化疗小鼠模型中,已显示出与利福平联合使用时具有协同杀菌抗结核活性。我们推测这种协同作用将产生比阿培南/利福平对利福平耐药结核分枝杆菌的活性。

目的

我们的目的是在体外和小鼠模型中评估比阿培南/利福平对低水平和高水平利福平耐药结核分枝杆菌菌株的协同作用。

方法

使用三株结核分枝杆菌评估比阿培南/利福平的活性:115R菌株(低水平利福平耐药);124R菌株(高水平利福平耐药);以及药物敏感的H37Rv亲本菌株。通过棋盘滴定法在体外评估比阿培南/利福平的协同作用。在体内,我们首先在小鼠模型中进行了比阿培南针对H37Rv的剂量范围实验。然后我们评估了比阿培南/利福平在感染每种结核分枝杆菌菌株的小鼠中的活性。

结果

在体外,观察到比阿培南和利福平对H37Rv和115R菌株有协同作用。在体内,比阿培南对H37Rv表现出明显的剂量依赖性活性,所有比阿培南剂量均与单独使用利福平一样有效或更有效。在小鼠模型中,比阿培南和利福平对H37Rv具有协同杀菌活性;在感染任何一种利福平耐药菌株的小鼠中均未观察到协同作用。单独使用比阿培南对所有三株菌株均有活性。

结论

我们的临床前实验表明,比阿培南有潜力用作抗结核药物,包括用于治疗利福平耐药结核病。因此,比阿培南有望重新用作治疗耐药结核病的“新”且急需的药物。

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