Chen Junjun, Zhang Huan, Liao Xuelian
Department of Critical Care Medicine, West China Hospital, Sichuan University, Chengdu, People's Republic of China.
Department of Critical Care Medicine, West China Tianfu Hospital of Sichuan University, Chengdu, People's Republic of China.
Infect Drug Resist. 2023 Aug 11;16:5243-5249. doi: 10.2147/IDR.S418523. eCollection 2023.
Hypervirulent (hvKP), especially multidrug-resistant hvKP (MDR-hvKP) infections, are distributed globally, and lead to several outbreaks with high pathogenicity and mortality in immunocompetent individuals. This is usually characterized by a rapidly metastatic spread resulting in multiple pyogenic tissue abscesses. To date, even though the explanation of hypervirulent factors of hvKP has been identified, it still remains to be fully understood. The most common key virulence agents of hvKP included (1) siderophore systems for iron acquisition, (2) increased capsule production, (3) the colibactin toxin, (4) hypermucoviscosity, and so on. Several hypervirulence factors have been renewed, and the evolution of MDR-hvKP has been deeply explored recently. We aim to describe a chain of key virulence agents attributed to the lethality of hvKP and MDR-hvKP. In this review, recent advances in renewed factors in hypervirulence were summarized, and potential therapeutic targets are explored. Novel co-existence of hypervirulence agents and multidrug-resistant elements, even the superplasmid, was screened. Superplasmid simultaneously harbours hypervirulence and multidrug-resistant genes and can mobile autonomously by its complete conjugative elements. Research into related immunity has also gained traction, which may cause multiple invasive infections with higher mortality rates than classical ones, such as neutrophil- and complement-mediated activity. The evolution of virulence and multidrug resistance is accelerating. More reliable methods for identifying hvKP or MDR-hvKP must be investigated. Furthermore, it is critical to investigate innovative treatment targets in the future.
高毒力肺炎克雷伯菌(hvKP),尤其是多重耐药性hvKP(MDR-hvKP)感染在全球范围内均有分布,并在免疫功能正常的个体中引发了多起具有高致病性和高死亡率的疫情。其通常的特征是迅速发生转移性扩散,导致多处化脓性组织脓肿。迄今为止,尽管已经确定了hvKP的高毒力因子的解释,但仍有待充分理解。hvKP最常见的关键毒力因子包括:(1)用于获取铁的铁载体系统;(2)荚膜产量增加;(3)大肠杆菌素毒素;(4)高黏液性等。一些高毒力因子已被更新,并且最近对MDR-hvKP的进化进行了深入探索。我们旨在描述一系列归因于hvKP和MDR-hvKP致死性的关键毒力因子。在本综述中,总结了高毒力更新因子的最新进展,并探索了潜在的治疗靶点。筛选了高毒力因子与多重耐药元件甚至超级质粒的新共存情况。超级质粒同时携带高毒力和多重耐药基因,并可通过其完整的接合元件自主移动。对相关免疫的研究也受到了关注,这可能导致比经典感染更高死亡率的多种侵袭性感染,如中性粒细胞和补体介导的活性。毒力和多重耐药性的进化正在加速。必须研究更可靠的鉴定hvKP或MDR-hvKP的方法。此外,未来研究创新治疗靶点至关重要。