Jia Yuqian, Zheng Zhiwan, Yang Bingqing, Zhang Haijie, Wang Zhiqiang, Liu Yuan
Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses College of Veterinary Medicine Yangzhou University YangzhouChina.
Department of Pathogenic Biology West China School of Basic Medical Sciences and Forensic Medicine Sichuan University ChengduChina.
Transbound Emerg Dis. 2024 May 30;2024:7063673. doi: 10.1155/2024/7063673. eCollection 2024.
The dissemination of antimicrobial resistance (AMR) severely degrades the performance of antibiotics and constantly paralyzes the global health system. In particular, plasmid-mediated transfer of antibiotic resistance genes (ARGs) across bacteria is recognized as the primary driver. Therefore, antiplasmid transfer approaches are urgently warranted to resolve this intractable problem. Herein, we demonstrated the potential of azidothymidine (AZT), an FDA-approved anti-HIV drug, as a broad-spectrum horizontal transfer inhibitor to effectively prevent the transmission of multiple ARGs, including , , and (X4), both and . It was also noteworthy that the inhibitory effect of AZT was proved to be valid within and across bacterial genera under different mating conditions. Mechanistic studies revealed that AZT dissipated bacterial proton motive force, which was indispensable for ATP synthesis and flagellar motility. In addition, AZT downregulated bacterial secretion systems involving general and type IV secretion systems (T4SS). Furthermore, the thymidine kinase, which is associated with DNA synthesis, turned out to be the potential target of AZT. Collectively, our work demonstrates the broad inhibitory effect of AZT in preventing ARGs transmission, opening new horizons for controlling AMR.
抗菌药物耐药性(AMR)的传播严重降低了抗生素的效能,并持续使全球卫生系统陷入瘫痪。特别是,抗生素耐药基因(ARGs)通过质粒在细菌间的转移被认为是主要驱动因素。因此,迫切需要采用抗质粒转移方法来解决这一棘手问题。在此,我们证明了经美国食品药品监督管理局(FDA)批准的抗HIV药物叠氮胸苷(AZT)作为一种广谱水平转移抑制剂的潜力,它能有效防止多种ARGs的传播,包括blaNDM-1、blaKPC-2和mcr-1(X4),无论是在革兰氏阴性菌还是革兰氏阳性菌中。同样值得注意的是,在不同的接合条件下,AZT的抑制作用在细菌属内和跨细菌属中均被证明是有效的。机制研究表明,AZT消耗了细菌的质子动力势,而质子动力势对于ATP合成和鞭毛运动是必不可少的。此外,AZT下调了涉及一般分泌系统和IV型分泌系统(T4SS)的细菌分泌系统。此外,与DNA合成相关的胸苷激酶被证明是AZT的潜在靶点。总的来说,我们的工作证明了AZT在防止ARGs传播方面具有广泛的抑制作用,为控制AMR开辟了新的前景。