Synergistic oral beta-lactam combinations for treating tuberculosis

被引:0
作者
Quan, Diana H. [1 ]
Wang, Trixie [1 ]
Martinez, Elena [2 ]
Kim, Hannah Y. [3 ,4 ]
Sintchenko, Vitali [5 ]
Britton, Warwick J. [1 ,6 ]
Triccas, James A. [4 ,5 ]
Alffenaar, Jan-Willem C. [3 ,4 ,7 ]
机构
[1] Univ Sydney, Centenary Inst, TB Res Program, Sydney, NSW 2006, Australia
[2] Westmead Inst, Ctr Infect Dis & Microbiol, Westmead, NSW 2145, Australia
[3] Univ Sydney, Sch Pharm, Sydney, NSW 2006, Australia
[4] Univ Sydney, Sydney Infect Dis Inst, Fac Med & Hlth, Camperdown, NSW 2006, Australia
[5] Sch Med Sci, Fac Med & Hlth, Camperdown, NSW 2006, Australia
[6] Royal Prince Alfred Hosp, Dept Clin Immunol, Sydney, NSW 2050, Australia
[7] Westmead Hosp, Westmead, NSW 2145, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
tuberculosis; beta-lactam; synergy; combination therapy; MEROPENEM-CLAVULANATE; IN-VITRO; ANTIBIOTICS; RESISTANCE; AMOXICILLIN/CLAVULANATE; LEVOFLOXACIN; ANTAGONISM; SELECTION; AMIKACIN; REGIMENS;
D O I
10.1093/jambio/lxae255
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: The enormous burden of tuberculosis (TB) worldwide is a major challenge to human health, but the costs and risks associated with novel drug discovery have limited treatment options for patients. Repurposing existing antimicrobial drugs offers a promising avenue to expand TB treatment possibilities. This study aimed to explore the activity and synergy of beta-lactams in combination with a beta-lactamase inhibitor, which have been underutilized in TB treatment to date. Methods: Based on inhibitory concentration, oral bioavailability, and commercial availability, seven beta-lactams (cefadroxil, tebipenem, cephradine, cephalexin, cefdinir, penicillin V, and flucloxacillin), two beta-lactamase inhibitors (avibactam and clavulanate), and three second-line TB drugs (moxifloxacin, levofloxacin, and linezolid) were selected for combination in vitro testing against Mycobacterium tuberculosis H37Rv. Re- sazurin assays and colony forming unit enumeration were used to quantify drug efficacy, Chou-Talalay calculations were performed to identify drug synergy and Chou-Martin calculations were performed to quantify drug dose reduction index. Results: The order of activity of beta-lactams was cefadroxil > tebipenem > cephradine > cephalexin > cefdinir > penicillin V > flucloxacillin. The addition of clavulanate improved beta-lactam activity to a greater degree than the addition of avibactam. As a result, avibactam was excluded from further investigations, which focused on clavulanate. Synergy was demonstrated for cefdinir/cephradine, cefadroxil/tebipenem, cefadroxil/penicillin V, cefadroxil/cefdinir, cephalexin/tebipenem, cephalexin/penicillin V, cephalexin/cefdinir, cephalexin/cephradine, and cefadroxil/cephalexin, all with clavulanate. However, combining beta-lactams with moxifloxacin, levofloxacin, or linezolid resulted in antagonistic effects, except for the combinations of penicillin V/levofloxacin, penicillin V/moxifloxacin, and cefdinir/moxifloxacin. Conclusions: Beta-lactam synergy may provide viable combination therapies for the treatment of TB.
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页数:12
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