Kui You, Nurhidayah Binte Mohamed Yazid, Li Ming Chong, Lissa Hooi, Peter Wang, Isaiah Zhuang, Stephen Chua, Ethan Lim, Alrick Zi Xin Kok, Kalisvar Marimuthu, Shawn Vasoo, Oon Tek Ng, Conrad E Z Chan, Edward Kai-Hua Chow, Dean Ho
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引用次数: 0
摘要
抗菌药耐药性(AMR)是全球公共卫生面临的一个新威胁。具体来说,鲍曼不动杆菌(A. baumannii)是导致院内感染增加的主要病原体之一,它是一种革兰氏阴性杆菌,具有内在耐药机制,也可通过从其他细菌获得 AMR 基因而产生耐药性。更重要的是,它对近 90% 的标准疗法(SOC)抗菌药产生耐药性,导致临床疗效不理想,感染相关死亡率高达 30% 以上。目前,在这场不断扩大的抗 AMR 军备竞赛中,可持续地开发新型抗菌药物面临着越来越大的挑战。因此,我们需要一个可持续的工作流程,妥善管理医疗资源,超快速地设计出最佳药物组合,以实现有效治疗。本研究利用 IDentif.AI-AMR 平台从美国 FDA 批准的九种药物中找出了针对四种鲍曼不动杆菌临床分离株的有效治疗方案。值得注意的是,IDentif.AI精确定位的氨苄西林-舒巴坦/头孢哌酮和头孢哌酮/多粘菌素B/利福平组合对该细菌的抑制率分别达到了93.89 ± 5.95% 和 92.23 ± 11.89%,它们可能会使该适应症的治疗方案库更加多样化。此外,多粘菌素 B 联合利福平在所有测试的临床分离物中都表现出广泛的疗效和很强的协同作用,是治疗鲍曼不动杆菌的一种潜在策略。IDentif.AI确定的组合可能成为鲍曼不动杆菌的替代治疗策略。
Flash optimization of drug combinations for Acinetobacter baumannii with IDentif.AI-AMR.
Antimicrobial resistance (AMR) is an emerging threat to global public health. Specifically, Acinetobacter baumannii (A. baumannii), one of the main pathogens driving the rise of nosocomial infections, is a Gram-negative bacillus that displays intrinsic resistance mechanisms and can also develop resistance by acquiring AMR genes from other bacteria. More importantly, it is resistant to nearly 90% of standard of care (SOC) antimicrobial treatments, resulting in unsatisfactory clinical outcomes and a high infection-associated mortality rate of over 30%. Currently, there is a growing challenge to sustainably develop novel antimicrobials in this ever-expanding arms race against AMR. Therefore, a sustainable workflow that properly manages healthcare resources to ultra-rapidly design optimal drug combinations for effective treatment is needed. In this study, the IDentif.AI-AMR platform was harnessed to pinpoint effective regimens against four A. baumannii clinical isolates from a pool of nine US FDA-approved drugs. Notably, IDentif.AI-pinpointed ampicillin-sulbactam/cefiderocol and cefiderocol/polymyxin B/rifampicin combinations were able to achieve 93.89 ± 5.95% and 92.23 ± 11.89% inhibition against the bacteria, respectively, and they may diversify the reservoir of treatment options for the indication. In addition, polymyxin B in combination with rifampicin exhibited broadly applicable efficacy and strong synergy across all tested clinical isolates, representing a potential treatment strategy for A. baumannii. IDentif.AI-pinpointed combinations may potentially serve as alternative treatment strategies for A. baumannii.