Xu Chen, Dong Ning, Chen Kaichao, Yang Xuemei, Zeng Ping, Hou Changshun, Chi Chan Edward Wai, Yao Xi, Chen Sheng
Department of Infectious Diseases and Public Health, Jockey Club College of Veterinary Medicine and Life Sciences, City University of Hong Kong, Kowloon, Hong Kong.
State Key Lab of Chemical Biology and Drug Discovery, Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong.
iScience. 2022 Feb 8;25(3):103894. doi: 10.1016/j.isci.2022.103894. eCollection 2022 Mar 18.
The emergence of carbapenem-resistant hypervirulent (CR-hvKP) causing high mortality in clinical patients infers the urgent need for developing therapeutic agents. Here, we demonstrated vitamin C (VC) exhibited strong bactericidal, anti-biofilm, and virulence-suppressing effects on CR-hvKP. Our results showed such a bactericidal effect is dose-dependent both and in the mouse infection model and is associated with induction of reactive oxygen species (ROS) generation. In addition, VC inhibited biofilm formation of CR-hvKP through suppressing the production of exopolysaccharide (EPS). In addition, VC acted as an efflux pump inhibitor at subminimum inhibitory concentration (sub-MIC) to disrupt transportation of EPS and capsular polysaccharide to bacterial cell surface, thereby further inhibiting biofilm and capsule formation. Furthermore, virulence-associated genes in CR-hvKP exposed to sub-MIC of VC were downregulated. Our findings indicated VC could be an effective and safe therapeutic agent to treat CR-hvKP infections in urgent cases when all current treatment options fail.
耐碳青霉烯类高毒力肺炎克雷伯菌(CR-hvKP)的出现导致临床患者高死亡率,这表明迫切需要开发治疗药物。在此,我们证明维生素C(VC)对CR-hvKP具有强大的杀菌、抗生物膜和抑制毒力的作用。我们的结果表明,这种杀菌作用在体外和小鼠感染模型中均呈剂量依赖性,并且与活性氧(ROS)生成的诱导有关。此外,VC通过抑制胞外多糖(EPS)的产生来抑制CR-hvKP的生物膜形成。此外,VC在亚最小抑菌浓度(sub-MIC)下作为一种外排泵抑制剂,破坏EPS和荚膜多糖向细菌细胞表面的转运,从而进一步抑制生物膜和荚膜的形成。此外,暴露于VC亚MIC的CR-hvKP中的毒力相关基因被下调。我们的研究结果表明,在所有现有治疗方案均失败的紧急情况下,VC可能是治疗CR-hvKP感染的一种有效且安全的治疗药物。