Synergistic oral beta-lactam combinations for treating tuberculosis.

IF 3.2 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Journal of Applied Microbiology Pub Date : 2024-10-03 DOI:10.1093/jambio/lxae255
Diana H Quan, Trixie Wang, Elena Martinez, Hannah Y Kim, Vitali Sintchenko, Warwick J Britton, James A Triccas, Jan-Willem C Alffenaar
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Abstract

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. Resazurin 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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治疗结核病的协同口服β-内酰胺类复方制剂。
背景:全球结核病(TB)的巨大负担是人类健康面临的一大挑战,但与新药研发相关的成本和风险限制了患者的治疗选择。现有抗菌药物的再利用为扩大结核病的治疗范围提供了一条前景广阔的途径。本研究旨在探索β-内酰胺类药物与β-内酰胺酶抑制剂联用的活性和协同作用:方法:根据抑制浓度、口服生物利用度和商业供应情况,七种β-内酰胺类药物(头孢羟氨苄、替比培南、头孢拉定、头孢氨苄、头孢地尼、青霉素 V、氟氯西林)与两种β-内酰胺酶抑制剂(头孢氨苄、替比培南、头孢拉定、头孢地尼、青霉素 V、氟氯西林)联用、选择了两种β-内酰胺酶抑制剂(阿维巴坦和克拉维酸)和三种二线结核病药物(莫西沙星、左氧氟沙星和利奈唑胺)对 H37Rv 型结核分枝杆菌进行联合体外试验。瑞沙唑林检测和菌落形成单位(CFU)计数用于量化药物疗效,Chou-Talalay 计算用于确定药物协同作用,Chou-Martin 计算用于量化药物剂量减少指数(DRI):β-内酰胺类药物的活性顺序为头孢羟氨苄>替比培南>头孢拉定>头孢氨苄>头孢地尼>青霉素 V>氟氯西林。与添加阿维巴坦相比,添加克拉维酸能在更大程度上提高β-内酰胺的活性。因此,阿维菌素被排除在进一步研究之外,研究重点放在克拉维酸上。头孢地尼/头孢拉定、头孢羟氨苄/替比培南、头孢羟氨苄/青霉素 V、头孢羟氨苄/头孢地尼、头孢氨苄/替比培南、头孢氨苄/青霉素 V、头孢氨苄/头孢地尼、头孢氨苄/头孢拉定和头孢羟氨苄/头孢拉定均与克拉维酸产生协同作用。然而,β-内酰胺类药物与莫西沙星、左氧氟沙星或利奈唑胺合用会产生拮抗作用,但青霉素 V/来氟沙星、青霉素 V/莫西沙星和头孢地尼/莫西沙星合用除外:结论:β-内酰胺类药物的协同作用可为结核病的治疗提供可行的联合疗法。
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来源期刊
Journal of Applied Microbiology
Journal of Applied Microbiology 生物-生物工程与应用微生物
CiteScore
7.30
自引率
2.50%
发文量
427
审稿时长
2.7 months
期刊介绍: Journal of & Letters in Applied Microbiology are two of the flagship research journals of the Society for Applied Microbiology (SfAM). For more than 75 years they have been publishing top quality research and reviews in the broad field of applied microbiology. The journals are provided to all SfAM members as well as having a global online readership totalling more than 500,000 downloads per year in more than 200 countries. Submitting authors can expect fast decision and publication times, averaging 33 days to first decision and 34 days from acceptance to online publication. There are no page charges.
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