Kaushik Amit, Ammerman Nicole C, Tasneen Rokeya, Story-Roller Elizabeth, Dooley Kelly E, Dorman Susan E, Nuermberger Eric L, Lamichhane Gyanu
Center for Tuberculosis Research, Johns Hopkins University School of Medicine, 1550 Orleans Street, Baltimore, MD 21287, USA.
J Antimicrob Chemother. 2017 Aug 1;72(8):2320-2325. doi: 10.1093/jac/dkx152.
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 .
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.
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.
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.
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.
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。
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。
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。
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。
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。