Carbapenem-resistant Gram-negative bacteria exhibiting clinically undetected cefiderocol heteroresistance leads to treatment failure in a murine model of infection.

IF 4 2区 生物学 Q2 MICROBIOLOGY
Frontiers in Microbiology Pub Date : 2025-05-09 eCollection Date: 2025-01-01 DOI:10.3389/fmicb.2025.1496514
Hongwei Liu, Peng Zhou, Peng Ma, Yaqin Liu, Yingfeng Zhang, Qiwei Li, Lingqing Xu, Wenchang Yuan, Weiguo Yin, Linhai Li, Yang Lu
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引用次数: 0

Abstract

Introduction: Carbapenem-resistant (CR) Gram-negative pathogens are classified by the WHO as critical threats due to limited therapeutic options. Cefiderocol (CFD), a novel siderophore cephalosporin, shows promise but remains unapproved in China. This study investigated the prevalence, clinical impact, and genetic mechanisms of cefiderocol heteroresistance (CFD-HR) in CR and ESBL-producing clinical isolates from China, where CFD remains unapproved.

Methods: A total of 407 CR and ESBL-producing isolates were analyzed. CFD-HR was identified by population analysis profiles (PAPs). Clinical relevance was assessed through disk diffusion susceptibility testing, time-kill assays, and a murine peritonitis model. Genetic mechanisms and stability were elucidated by whole-genome sequencing (WGS) and fitness cost assays.

Results: CFD-HR prevalence was 17.4% (16/92) in carbapenem-resistant A. baumannii (CRAB), 27.9% (24/86) in carbapenem-resistant P. aeruginosa (CRPA), 23.8% (10/42) in carbapenem-resistant E. coli (CRE), and ≤10% (1/10 in ESBL-producing P. aeruginosa and 8/177 in ESBL-producing E. coli). Although 72.9% (43/59) of HR isolates were classified as CFD-susceptible by disk diffusion, time-kill assays showed that 66.7% (4/6) of HR strains required ≥8 mg/L CFD (vs. 4 mg/L for non-HR) to prevent regrowth. In vivo, CFD achieved 100% (3/3) survival in non-HR infections but only 16.7% (4/6) in HR-infected mice. WGS identified transient genetic alterations in HR subpopulations, including sitABCD duplications (CRE), oprD mutations (CRAB), and vgrG SNPs (CRPA), which reverted after antibiotic withdrawal. Fitness cost assays revealed unstable growth deficits in 33.3% (2/6) of HR subpopulations, correlating with genetic instability.

Discussion: These findings highlight the clinical significance of CFD-HR, even in susceptible isolates, and underscore the need for improved diagnostic methods to detect HR and monitor cross-resistance, offering critical insights for regions transitioning to CFD implementation.

碳青霉烯耐药革兰氏阴性菌表现出临床未检测到的头孢地罗异耐药性,导致小鼠感染模型治疗失败。
导言:由于治疗选择有限,耐碳青霉烯革兰氏阴性病原体被世卫组织列为严重威胁。Cefiderocol (CFD)是一种新型铁载体头孢菌素,前景光明,但仍未在中国获得批准。本研究调查了中国产CR和esbl临床分离株头孢地罗异耐药(CFD- hr)的患病率、临床影响和遗传机制,CFD尚未获得批准。方法:对407株产CR和esbl的分离株进行分析。通过种群分析概况(pap)确定了CFD-HR。通过磁盘扩散敏感性试验、时间杀伤试验和小鼠腹膜炎模型评估临床相关性。通过全基因组测序(WGS)和适应度成本分析阐明了遗传机制和稳定性。结果:耐碳青霉烯鲍曼假单胞菌(CRAB)、耐碳青霉烯铜绿假单胞菌(CRPA)、耐碳青霉烯大肠杆菌(CRE)的CFD-HR患病率分别为17.4%(16/92)、27.9%(24/86)、23.8%(10/42),且≤10%(产esbl铜绿假单胞菌1/10、产esbl大肠杆菌8/177)。尽管72.9%(43/59)的HR菌株对cd敏感,但时间杀伤试验显示,66.7%(4/6)的HR菌株需要≥8 mg/L的CFD才能阻止再生(非HR菌株为4 mg/L)。体内,CFD在非hr感染小鼠中达到100%(3/3)的存活率,而在hr感染小鼠中仅为16.7%(4/6)。WGS在HR亚群中发现了短暂的遗传改变,包括sitABCD重复(CRE)、oprD突变(CRAB)和vgrG snp (CRPA),这些改变在停药后恢复。适应度成本分析显示,33.3%(2/6)的HR亚群存在不稳定生长缺陷,这与遗传不稳定性有关。讨论:这些发现强调了CFD-HR的临床意义,即使在易感分离株中也是如此,并强调了改进诊断方法以检测HR和监测交叉耐药性的必要性,为向CFD实施过渡的地区提供了关键见解。
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
CiteScore
7.70
自引率
9.60%
发文量
4837
审稿时长
14 weeks
期刊介绍: Frontiers in Microbiology is a leading journal in its field, publishing rigorously peer-reviewed research across the entire spectrum of microbiology. Field Chief Editor Martin G. Klotz at Washington State University is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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