Klebsiella pneumoniae with Two Carbapenemases: Where Molecular Research Stands Now.

IF 2.9 3区 医学 Q2 INFECTIOUS DISEASES
Infection and Drug Resistance Pub Date : 2025-09-15 eCollection Date: 2025-01-01 DOI:10.2147/IDR.S537638
Qian Yu, Gaosha Li, Qianqian Xu, Yijun Zhu
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Abstract

Klebsiella pneumoniae is a significant pathogen causing various infections. Since the 1990s, carbapenem-resistant Klebsiella pneumoniae (CRKP) has threatened global health. Its main resistance mechanism is producing carbapenemases like KPC, NDM, OXA, IMP and VIM, which have different prevalent isoforms and resistance features. In China, KPC is the most common carbapenemase in CRKP, followed by metallo-β-lactamase (MBL). Alarmingly, an increasing number of K. pneumoniae strains carry two or more types of enzymes, making resistance more complex. This review summarizes the major carbapenemases carried by K. pneumoniae, their global spread, and plasmids of CRKP enzyme type combinations reported in existing studies. Common combinations such as KPC + metalloenzyme, bimetallic enzyme, and metalloenzyme + OXA-48 are discussed in detail, including their genetic environments and transfer characteristics. Whole genome sequencing technology plays a crucial role in studying drug resistance genes of K. pneumoniae, facilitating in - depth identification and analysis of bacteria, and being useful for outbreak investigation and epidemiological surveillance. In conclusion, resistance genes in K. pneumoniae are often located on mobile elements. Different resistance genes tend to be carried by specific plasmids, which have high transformation rates and little impact on host growth. In order to prevent the emergence of Klebsiella pneumoniae carrying multiple drug-resistant genes, several measures such as the rational use of antibiotics, earlier monitoring of the transmission trajectory of strains, and the prediction of the development direction of drug resistance as much as possible are particularly important in the world today.

Abstract Image

肺炎克雷伯菌与两种碳青霉烯酶:分子研究的现状。
肺炎克雷伯菌是引起多种感染的重要病原体。自20世纪90年代以来,耐碳青霉烯肺炎克雷伯菌(CRKP)已威胁到全球健康。其主要耐药机制是产生KPC、NDM、OXA、IMP和VIM等碳青霉烯酶,这些酶具有不同的流行亚型和耐药特征。在中国,CRKP中KPC是最常见的碳青霉烯酶,其次是金属β-内酰胺酶(MBL)。令人震惊的是,越来越多的肺炎克雷伯菌菌株携带两种或两种以上类型的酶,使耐药性更加复杂。本文综述了肺炎克雷伯菌携带的主要碳青霉烯酶及其全球传播,以及现有研究报道的CRKP酶型组合质粒。详细讨论了KPC +金属酶、双金属酶、金属酶+ OXA-48等常见的组合,包括它们的遗传环境和转移特性。全基因组测序技术在研究肺炎克雷伯菌耐药基因、促进细菌的深入鉴定和分析、开展疫情调查和流行病学监测等方面具有重要意义。总之,肺炎克雷伯菌的耐药基因通常位于可移动元件上。不同的抗性基因往往由特定的质粒携带,转化速率高,对寄主生长影响小。为了防止携带多重耐药基因的肺炎克雷伯菌的出现,合理使用抗生素、尽早监测菌株传播轨迹、尽可能预测耐药发展方向等几项措施在当今世界尤为重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Infection and Drug Resistance
Infection and Drug Resistance Medicine-Pharmacology (medical)
CiteScore
5.60
自引率
7.70%
发文量
826
审稿时长
16 weeks
期刊介绍: About Journal Editors Peer Reviewers Articles Article Publishing Charges Aims and Scope Call For Papers ISSN: 1178-6973 Editor-in-Chief: Professor Suresh Antony An international, peer-reviewed, open access journal that focuses on the optimal treatment of infection (bacterial, fungal and viral) and the development and institution of preventative strategies to minimize the development and spread of resistance.
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