齐多夫定与硝基呋喃妥因或奥马他环素的协同组合:对耐多药肺炎克雷伯菌的体外和小鼠尿道或肺部感染评估。

IF 4.1 2区 医学 Q2 MICROBIOLOGY
Ping Tian, Qing-Qing Li, Ming-Juan Guo, Yun-Zhu Zhu, Rong-Qing Zhu, Ya-Qin Guo, Yi Yang, Yan-Yan Liu, Liang Yu, Ya-Sheng Li, Jia-Bin Li
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引用次数: 0

摘要

有限的治疗方案和耐多药(MDR)肺炎克雷伯氏菌给治疗带来了巨大挑战,突出了对新方法的需求。药物再利用是增强多种抗生素活性的有效手段。本研究的目的是在药物再利用的基础上确定针对肺炎克雷伯菌的新型协同药物组合。我们利用临床分离的肺炎克雷伯菌 GN 172867 MDR 菌株来确定齐多夫定(AZT)的逆转抗药性活性。我们使用棋盘格法、生长曲线以及评估生物膜的结晶紫测定法,检验了 AZT 与硝基呋喃妥因(NIT)和奥美拉唑霉素(OMC)等多种抗生素的联合作用。在 12 个肺炎双球菌分离物中进行了体外组合活性测试。体内小鼠尿道和肺部感染模型分别用于评估 AZT + NIT 和 AZT + OMC 的治疗效果。部分抑制浓度指数和生长曲线表明,AZT 与 NIT 或 OMC 对肺炎克雷伯菌株有协同作用。此外,AZT + NIT 还能抑制生物膜的形成并清除成熟的生物膜。在体内,与未经治疗的 GN 172867 感染小鼠相比,AZT + NIT 和 AZT + OMC 治疗降低了多个组织中的菌落计数(P < 0.05)以及膀胱和肾脏的病理评分(P < 0.05),并提高了 60% 的存活率(P < 0.05)。这项研究评估了 AZT 与抗生素联合治疗耐药肺炎双球菌感染的效果,并发现了治疗急性尿路感染的新型药物组合。这些研究结果表明,AZT 可发挥显著的抗耐药性活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Zidovudine in synergistic combination with nitrofurantoin or omadacycline: in vitro and in murine urinary tract or lung infection evaluation against multidrug-resistant Klebsiella pneumoniae.

Limited treatment options and multidrug-resistant (MDR) Klebsiella pneumoniae present a significant therapeutic challenge, underscoring the need for novel approaches. Drug repurposing is a promising tool for augmenting the activity of many antibiotics. This study aimed to identify novel synergistic drug combinations against K. pneumoniae based on drug repurposing. We used the clinically isolated GN 172867 MDR strain of K. pneumoniae to determine the reversal resistance activity of zidovudine (AZT). The combined effects of AZT and various antibiotics, including nitrofurantoin (NIT) and omadacycline (OMC), were examined using the checkerboard method, growth curves, and crystal violet assays to assess biofilms. An in vitro combination activity testing was carried out in 12 isolates of K. pneumoniae. In vivo murine urinary tract and lung infection models were used to evaluate the therapeutic effects of AZT + NIT and AZT + OMC, respectively. The fractional inhibitory concentration index and growth curve demonstrated that AZT synergized with NIT or OMC against K. pneumoniae strains. In addition, AZT + NIT inhibited biofilm formation and cleared mature biofilms. In vivo, compared with untreated GN 172867-infected mice, AZT + NIT and AZT + OMC treatment decreased colony counts in multiple tissues (P < 0.05) and pathological scores in the bladder and kidneys (P < 0.05) and increased the survival rate by 60% (P < 0.05). This study evaluated the combination of AZT and antibiotics to treat drug-resistant K. pneumoniae infections and found novel drug combinations for the treatment of acute urinary tract infections. These findings suggest that AZT may exert significant anti-resistance activity.

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来源期刊
CiteScore
10.00
自引率
8.20%
发文量
762
审稿时长
3 months
期刊介绍: Antimicrobial Agents and Chemotherapy (AAC) features interdisciplinary studies that build our understanding of the underlying mechanisms and therapeutic applications of antimicrobial and antiparasitic agents and chemotherapy.
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