MGEs介导多重耐药高毒力肺炎克雷伯菌耐药与毒力表型汇聚机制的研究进展

Research progress in MGEs-mediated multidrug-resistant hypervirulent Klebsiella pneumoniae drug resistance and virulence phenotype convergence mechanism

  • 摘要: 多重耐药高毒力肺炎克雷伯菌(MDR-HvKP)兼具耐药性及高毒力双重特性,其进化机制主要包括高毒力肺炎克雷伯菌获得耐药质粒、多重耐药肺炎克雷伯菌获得毒力质粒以及形成毒力-耐药杂合质粒。可移动遗传元件在这一过程中发挥关键作用。此外,PhoP/Q、Rcs等调控系统也参与进化调控。目前正积极开展分离鉴定菌株、开发新型抗菌药物及噬菌体疗法等应对策略。MDR-HvKP传播风险高、临床治疗难度大,给临床防控带来严峻挑战。深入研究MDR-HvKP的形成机制并研发新型治疗策略,对临床防控和治疗意义重大。

     

    Abstract: Multidrug-resistant hypervirulent Klebsiella pneumoniae (MDR-HvKP) possesses dual characteristics of drug resistance and high virulence. Its evolutionary mechanisms mainly include the acquisition of drug-resistant plasmids by hypervirulent K. pneumoniae, the acquisition of virulence plasmids by multidrug-resistant K. pneumoniae and the formation of virulence-drug resistance hybrid plasmids. Mobile genetic elements (MGEs) play a key role in this process. In addition, regulatory systems such as PhoP/Q and Rcs also participate in evolutionary regulation. Currently, coping strategies such as strain isolation and identification, development of novel antibacterial drugs and phage therapy are being actively conducted. MDR-HvKP poses a high transmission risk and is challenging to treat clinically, posing severe challenges to clinical prevention and control. In-depth research on the formation mechanism of MDR-HvKP and the development of novel treatment strategies are of great significance for clinical prevention, control and treatment.

     

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