Suppr超能文献

齐多夫定与呋喃妥因或奥马环素联合增效作用:在治疗多药耐药 感染的鼠尿路感染或肺部感染中的评估

Zidovudine in synergistic combination with nitrofurantoin or omadacycline: and in murine urinary tract or lung infection evaluation against multidrug-resistant .

机构信息

Department of Infectious Diseases & Anhui Center for Surveillance of Bacterial Resistance, The First Affiliated Hospital of Anhui Medical University, Hefei, China.

Anhui Province Key Laboratory of Infectious Diseases and Institute of Bacterial Resistance, Anhui Medical University, Hefei, China.

出版信息

Antimicrob Agents Chemother. 2024 Oct 8;68(10):e0034424. doi: 10.1128/aac.00344-24. Epub 2024 Aug 28.

Abstract

Limited treatment options and multidrug-resistant (MDR) 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 based on drug repurposing. We used the clinically isolated GN 172867 MDR strain of 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 combination activity testing was carried out in 12 isolates of 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 strains. In addition, AZT + NIT inhibited biofilm formation and cleared mature biofilms. , compared with untreated GN 172867-infected mice, AZT + NIT and AZT + OMC treatment decreased colony counts in multiple tissues ( < 0.05) and pathological scores in the bladder and kidneys ( < 0.05) and increased the survival rate by 60% ( < 0.05). This study evaluated the combination of AZT and antibiotics to treat drug-resistant 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.

摘要

治疗选择有限且存在多药耐药(MDR),这对治疗提出了重大挑战,突显了需要新的方法。药物重定位是增强许多抗生素活性的有前途的工具。本研究旨在基于药物重定位确定针对耐多药 的新型协同药物组合。我们使用临床分离的耐多药 GN 172867 株 来确定齐多夫定(AZT)逆转耐药性的活性。使用棋盘法、生长曲线和结晶紫测定法检查 AZT 与各种抗生素(包括呋喃妥因(NIT)和奥马环素(OMC))的联合效应,以评估生物膜。在 12 株 鼠尿路感染分离株中进行了 组合活性测试,并使用肺部感染模型分别评估 AZT+NIT 和 AZT+OMC 的治疗效果。分数抑制浓度指数和生长曲线表明 AZT 与 NIT 或 OMC 协同作用对抗 株。此外,AZT+NIT 抑制生物膜形成并清除成熟生物膜。与未处理的 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(<0.05)和膀胱和肾脏中的病理评分(<0.05),并使存活率提高了 60%(<0.05)。本研究评估了 AZT 与抗生素联合治疗耐药 感染的效果,并发现了治疗急性尿路感染的新药物组合。这些发现表明 AZT 可能具有显著的抗耐药活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0761/11459972/3548af9c99f4/aac.00344-24.f001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验