Jia Yaping, Fan Junsheng, Tan Zhili, Li Anqi, He Siyuan, Lin Yani, Li Juan, Zhang Zhemin, Li Bing, Chu Haiqing
Department of Respiratory and Critical Care Medicine, Shanghai Pulmonary Hospital, School of Medicine,Tongji University, Shanghai, China.
School of Medicine, Tongji University, Shanghai, China.
Antimicrob Agents Chemother. 2025 Jul 2;69(7):e0024925. doi: 10.1128/aac.00249-25. Epub 2025 May 23.
Antibiotic therapy for infections is challenging due to resistance of the organism to many clinically available antimicrobials. Here, the efficacy of NITD-916, an enoyl-ACP reductase inhibitor, in preventing growth and is demonstrated. The minimal inhibitory concentrations (MICs) of NITD-916 for 12 non-tuberculosis mycobacteria (NTM) reference strains and a collection of 194 clinical isolates were determined using the broth microdilution method. Compatibility of NITD-916 with 10 clinically important antibiotics was ascertained by checkerboard assay. The activity of NITD-916 against growing in cultured macrophages was also evaluated. Finally, the potency of NITD-916 was determined in a mouse model that mimicked an acute pulmonary infection. NITD-916 was bacteriostatic for replicating expressing a MIC of 0.125 mg/L and a MIC of 1 mg/L against the screened clinical isolates. Furthermore, NITD-916 synergized with clarithromycin in treating 2 out of 5 subsp. strains. NITD-916 was active against replicating in both cultured macrophages and infected mice. The administration of 100 mg/kg NITD-916 for 14 days resulted in a 5.6 log colony-forming units (CFUs) reduction in the bacterial load in mouse lung tissue. NITD-916 is active against and and may be used potentially to treat diseases.
由于病原体对许多临床可用抗菌药物产生耐药性,因此针对感染的抗生素治疗具有挑战性。在此,烯酰-ACP还原酶抑制剂NITD-916在预防生长方面的疗效得到了证实。使用肉汤微量稀释法测定了NITD-916对12株非结核分枝杆菌(NTM)参考菌株和194株临床分离株的最低抑菌浓度(MIC)。通过棋盘法确定了NITD-916与10种临床重要抗生素的相容性。还评估了NITD-916对在培养巨噬细胞中生长的活性。最后,在模拟急性肺部感染的小鼠模型中确定了NITD-916的效力。NITD-916对正在复制的具有抑菌作用,对筛选出的临床分离株的MIC为0.125 mg/L,对的MIC为1 mg/L。此外,NITD-916在治疗5个亚种中的2个菌株时与克拉霉素具有协同作用。NITD-916对在培养巨噬细胞和感染小鼠中复制的均具有活性。以100 mg/kg的剂量给予NITD-916,持续14天,可使小鼠肺组织中的细菌载量减少5.6个对数集落形成单位(CFU)。NITD-916对和均具有活性,可能潜在地用于治疗疾病。