Pseudomonas aeruginosa chronic infections in patients with bronchiectasis: a silent reservoir of carbapenemase-producing epidemic high-risk clones.

IF 3.7 Q2 INFECTIOUS DISEASES
JAC-Antimicrobial Resistance Pub Date : 2025-04-08 eCollection Date: 2025-04-01 DOI:10.1093/jacamr/dlaf053
Alba Muñoz-Santa, Carla López-Causapé, Alba Bellés, Xavier Gómez-Arbonés, Sara Cortés-Lara, Mercè García-González, Ricardo Pifarré-Teixidó, Antonio Oliver
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Abstract

Objectives: Pseudomonas aeruginosa is one of the major drivers of morbidity and mortality in patients with chronic underlying diseases. Whereas cystic fibrosis (CF) P. aeruginosa strains have been well studied, non-CF bronchiectasis isolates have received less scientific attention.

Methods: We determined the antibiotic susceptibility profiles of a collection of 100 P. aeruginosa isolates recovered from a total of 100 non-CF bronchiectasis patients attending a Catalonian hospital. All carbapenemase-producing isolates were characterized by WGS.

Results: Twelve isolates were classified as MDR (12%) and six were found to be carbapenemase (VIM-2) producers (6%). Of note, two of the VIM-2-producing isolates were carbapenem susceptible due to the presence of inactivating mutations in MexAB-OprM efflux pump components. These isolates exhibited properties of chronic P. aeruginosa isolates, such as mutator or mucoid phenotypes that are associated with persistent infections despite intensive antibiotic therapies. The phylogenetic analysis evidenced that all VIM-2 isolates belonged to the high-risk clone ST235. Core-genome MLST analysis revealed 7-260 allelic differences, arguing against recent transmission but a common source of infection or an ancient interpatient transmission event could not be ruled out.

Conclusions: Altogether, these findings suggest that P. aeruginosa chronic respiratory infections can be an important and silent reservoir of transferable resistance determinants and P. aeruginosa high-risk clones, thus contributing to their increased resistance and worldwide dissemination.

支气管扩张患者的铜绿假单胞菌慢性感染:产生碳青霉烯酶的流行病高危克隆的沉默库。
目的:铜绿假单胞菌是慢性基础疾病患者发病和死亡的主要原因之一。对囊性纤维化(CF)铜绿假单胞菌菌株的研究较多,而对非囊性纤维化支气管扩张症分离菌株的研究较少:方法:我们对从加泰罗尼亚一家医院的 100 名非 CF 支气管扩张症患者中分离出的 100 株铜绿假单胞菌进行了抗生素敏感性分析。所有产碳青霉烯酶的分离株均通过 WGS 鉴定:结果:12 个分离菌株被归类为 MDR(12%),6 个分离菌株被发现产碳青霉烯酶(VIM-2)(6%)。值得注意的是,由于 MexAB-OprM 外排泵成分发生了失活突变,其中两个产生 VIM-2 的分离株对碳青霉烯类有敏感性。这些分离物表现出慢性铜绿假单胞菌分离物的特性,如突变体或粘液表型,这与使用强化抗生素治疗后仍出现持续感染有关。系统发育分析表明,所有 VIM-2 分离物都属于高风险克隆 ST235。核心基因组 MLST 分析显示,有 7-260 个等位基因存在差异,这表明病毒不是近期传播的,但也不能排除存在共同感染源或古老的患者间传播事件:总之,这些研究结果表明,铜绿假单胞菌慢性呼吸道感染可能是可转移耐药决定簇和铜绿假单胞菌高危克隆的一个重要而沉默的贮藏库,从而导致其耐药性增强并在全球范围内传播。
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
5.30
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0.00%
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审稿时长
16 weeks
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