College of Veterinary Medicine, Yangzhou University, Yangzhou, Jiangsu, China.
Jiangsu Co-Innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou, Jiangsu, China.
Commun Biol. 2020 Apr 3;3(1):162. doi: 10.1038/s42003-020-0877-5.
Recent emergence of high-level tigecycline resistance mediated by Tet(X3/X4) in Enterobacteriaceae undoubtably constitutes a serious threat for public health worldwide. Antibiotic adjuvant strategy makes antibiotic more effective against these resistant pathogens through interfering intrinsic resistance mechanisms or enhancing antibiotic actions. Herein, we screened a collection of drugs to identify compounds that are able to restore tigecycline activity against resistant pathogens. Encouragingly, we discovered that anti-HIV agent azidothymidine dramatically potentiates tigecycline activity against clinically resistant bacteria. Meanwhile, addition of azidothymidine prevents the evolution of tigecycline resistance in E. coli and the naturally occurring horizontal transfer of tet(X4). Evidence demonstrated that azidothymidine specifically inhibits DNA synthesis and suppresses resistance enzyme activity. Moreover, in in vivo infection models by Tet(X4)-expression E. coli, the combination of azidothymidine and tigecycline achieved remarkable treatment benefits including increased survival and decreased bacterial burden. These findings provide an effective regimen to treat infections caused by tigecycline-resistant Escherichia coli.
最近,肠杆菌科中由 Tet(X3/X4)介导的高水平替加环素耐药的出现无疑对全球公共卫生构成了严重威胁。抗生素辅助策略通过干扰固有耐药机制或增强抗生素作用,使抗生素对这些耐药病原体更有效。在此,我们筛选了一组药物,以确定能够恢复替加环素对耐药病原体活性的化合物。令人鼓舞的是,我们发现抗 HIV 药物叠氮胸苷可显著增强替加环素对临床耐药菌的活性。同时,添加叠氮胸苷可防止大肠埃希菌中替加环素耐药的进化和 tet(X4)的自然水平转移。证据表明,叠氮胸苷特异性抑制 DNA 合成并抑制耐药酶活性。此外,在 Tet(X4)-表达大肠埃希菌的体内感染模型中,叠氮胸苷和替加环素的联合使用在治疗方面取得了显著的疗效,包括提高生存率和降低细菌负荷。这些发现为治疗由替加环素耐药的大肠埃希菌引起的感染提供了一种有效的方案。