Pu Danni, Zhao Jiankang, Chang Kang, Zhuo Xianxia, Cao Bin
Graduate School of Peking Union Medical College, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing 100730, China; Laboratory of Clinical Microbiology and Infectious Diseases, Department of Pulmonary and Critical Care Medicine, Center of Respiratory Medicine, National Clinical Research Center for Respiratory Diseases, National Center for Respiratory Medicine, China-Japan Friendship Hospital, Beijing 100029, China; Institute of Respiratory Medicine, Chinese Academy of Medical Sciences, Beijing 100029, China.
Laboratory of Clinical Microbiology and Infectious Diseases, Department of Pulmonary and Critical Care Medicine, Center of Respiratory Medicine, National Clinical Research Center for Respiratory Diseases, National Center for Respiratory Medicine, China-Japan Friendship Hospital, Beijing 100029, China; Institute of Respiratory Medicine, Chinese Academy of Medical Sciences, Beijing 100029, China.
Sci Bull (Beijing). 2023 Nov 15;68(21):2658-2670. doi: 10.1016/j.scib.2023.09.040. Epub 2023 Sep 29.
Although hypervirulent Klebsiella pneumoniae (hvKP) can produce community-acquired infections that are fatal in young and adult hosts, such as pyogenic liver abscess, endophthalmitis, and meningitis, it has historically been susceptible to antibiotics. Carbapenem-resistant K. pneumoniae (CRKP) is usually associated with urinary tract infections acquired in hospitals, pneumonia, septicemias, and soft tissue infections. Outbreaks and quick spread of CRKP in hospitals have become a major challenge in public health due to the lack of effective antibacterial treatments. In the early stages of K. pneumoniae development, HvKP and CRKP first appear as distinct routes. However, the lines dividing the two pathotypes are vanishing currently, and the advent of carbapenem-resistant hypervirulent K. pneumoniae (CR-hvKP) is devastating as it is simultaneously multidrug-resistant, hypervirulent, and highly transmissible. Most CR-hvKP cases have been reported in Asian clinical settings, particularly in China. Typically, CR-hvKP develops when hvKP or CRKP acquires plasmids that carry either the carbapenem-resistance gene or the virulence gene. Alternatively, classic K. pneumoniae (cKP) may acquire a hybrid plasmid carrying both genes. In this review, we provide an overview of the key antimicrobial resistance mechanisms, virulence factors, clinical presentations, and outcomes associated with CR-hvKP infection. Additionally, we discuss the possible evolutionary processes and prevalence of CR-hvKP in China. Given the wide occurrence of CR-hvKP, continued surveillance and control measures of such organisms should be assigned a higher priority.
尽管高毒力肺炎克雷伯菌(hvKP)可引发社区获得性感染,在年轻和成年宿主中导致致命后果,如化脓性肝脓肿、眼内炎和脑膜炎,但从历史上看它对抗生素敏感。耐碳青霉烯类肺炎克雷伯菌(CRKP)通常与医院获得性尿路感染、肺炎、败血症及软组织感染有关。由于缺乏有效的抗菌治疗方法,CRKP在医院内的暴发和快速传播已成为公共卫生领域的一项重大挑战。在肺炎克雷伯菌发展的早期阶段,hvKP和CRKP最初表现为不同的路径。然而,目前区分这两种致病型的界限正在消失,耐碳青霉烯类高毒力肺炎克雷伯菌(CR-hvKP)的出现具有毁灭性,因为它同时具有多重耐药性、高毒力和高传播性。大多数CR-hvKP病例是在亚洲临床环境中报道的,尤其是在中国。通常,当hvKP或CRKP获得携带碳青霉烯类耐药基因或毒力基因的质粒时,CR-hvKP就会产生。或者,经典肺炎克雷伯菌(cKP)可能获得携带这两种基因的杂交质粒。在本综述中,我们概述了与CR-hvKP感染相关的关键抗菌耐药机制、毒力因子、临床表现及转归。此外,我们还讨论了CR-hvKP在中国可能的进化过程和流行情况。鉴于CR-hvKP广泛存在,对此类病原体持续进行监测和采取控制措施应被赋予更高优先级。