Department of Microbiology & Immunology, McGill University, Montréal, Canada.
Infectious Diseases and Immunity in Global Health Program, Research Institute of the McGill University Health Centre, Montréal, Canada.
PLoS Pathog. 2021 Oct 12;17(10):e1009965. doi: 10.1371/journal.ppat.1009965. eCollection 2021 Oct.
Mycobacterium abscessus is the most common rapidly growing non-tuberculous mycobacteria to cause pulmonary disease in patients with impaired lung function such as cystic fibrosis. M. abscessus displays high intrinsic resistance to common antibiotics and inducible resistance to macrolides like clarithromycin. As such, M. abscessus is clinically resistant to the entire regimen of front-line M. tuberculosis drugs, and treatment with antibiotics that do inhibit M. abscessus in the lab results in cure rates of 50% or less. Here, we identified epetraborole (EPT) from the MMV pandemic response box as an inhibitor against the essential protein leucyl-tRNA synthetase (LeuRS) in M. abscessus. EPT protected zebrafish from lethal M. abscessus infection and did not induce self-resistance nor against clarithromycin. Contrary to most antimycobacterials, the whole-cell activity of EPT was greater against M. abscessus than M. tuberculosis, but crystallographic and equilibrium binding data showed that EPT binds LeuRSMabs and LeuRSMtb with similar residues and dissociation constants. Since EPT-resistant M. abscessus mutants lost LeuRS editing activity, these mutants became susceptible to misaminoacylation with leucine mimics like the non-proteinogenic amino acid norvaline. Proteomic analysis revealed that when M. abscessus LeuRS mutants were fed norvaline, leucine residues in proteins were replaced by norvaline, inducing the unfolded protein response with temporal changes in expression of GroEL chaperonins and Clp proteases. This supports our in vitro data that supplementation of media with norvaline reduced the emergence of EPT mutants in both M. abscessus and M. tuberculosis. Furthermore, the combination of EPT and norvaline had improved in vivo efficacy compared to EPT in a murine model of M. abscessus infection. Our results emphasize the effectiveness of EPT against the clinically relevant cystic fibrosis pathogen M. abscessus, and these findings also suggest norvaline adjunct therapy with EPT could be beneficial for M. abscessus and other mycobacterial infections like tuberculosis.
脓肿分枝杆菌是最常见的引起肺功能受损患者(如囊性纤维化患者)肺部疾病的快速生长非结核分枝杆菌。脓肿分枝杆菌对常见抗生素具有固有耐药性,并对大环内酯类抗生素(如克拉霉素)表现出诱导耐药性。因此,脓肿分枝杆菌对一线抗结核药物的整个方案均具有临床耐药性,而在实验室中抑制脓肿分枝杆菌的抗生素治疗的治愈率仅为 50%或更低。在这里,我们从 MMV 大流行应对工具箱中鉴定出 epetraborole (EPT) 是一种抑制脓肿分枝杆菌必需蛋白亮氨酰-tRNA 合成酶 (LeuRS) 的抑制剂。EPT 可保护斑马鱼免受致命的脓肿分枝杆菌感染,且不会诱导自身耐药性或对克拉霉素耐药。与大多数抗分枝杆菌药物相反,EPT 对脓肿分枝杆菌的全细胞活性大于结核分枝杆菌,但晶体学和平衡结合数据表明,EPT 与 LeuRSMabs 和 LeuRSMtb 结合的残基和解离常数相似。由于 EPT 耐药的脓肿分枝杆菌突变体失去 LeuRS 编辑活性,这些突变体对亮氨酸类似物(如非蛋白氨基酸正缬氨酸)的错误氨酰化作用变得敏感。蛋白质组学分析表明,当脓肿分枝杆菌 LeuRS 突变体被正缬氨酸喂养时,蛋白质中的亮氨酸残基被正缬氨酸取代,导致未折叠蛋白反应,GroEL 伴侣蛋白和 Clp 蛋白酶的表达随时间发生变化。这支持了我们的体外数据,即培养基中补充正缬氨酸可减少脓肿分枝杆菌和结核分枝杆菌中 EPT 突变体的出现。此外,与 EPT 相比,EPT 与正缬氨酸联合使用在脓肿分枝杆菌感染的小鼠模型中具有更好的体内疗效。我们的研究结果强调了 EPT 对临床相关囊性纤维化病原体脓肿分枝杆菌的有效性,并且这些发现还表明,EPT 联合正缬氨酸辅助治疗可能对脓肿分枝杆菌和其他分枝杆菌感染(如结核病)有益。