Characterization of Carbapenemase-producing Enterobacterales isolated from patients returning from Sub-Saharan Africa, France, 2015–2022

粘菌素 阿米卡星 头孢他啶 抗生素 基因分型 肺炎克雷伯菌 生物 抗生素耐药性 微生物学 阿维巴坦 基因型 遗传学 基因 铜绿假单胞菌 细菌 大肠杆菌
作者
Corentin Poignon,Laurent Dortet,A. Birer,Inès Rezzoug,Cécile Emeraud,Delphine Girlich,Thierry Naas,Rémy A. Bonnin,Agnès B. Jousset
出处
期刊:Journal of Antimicrobial Chemotherapy [Oxford University Press]
标识
DOI:10.1093/jac/dkaf206
摘要

Abstract Objectives The rise of carbapenemase-producing Enterobacterales (CPE) represents a major public health threat, as highlighted in numerous reports from international health organizations. However, a significant data gap remains for certain regions, particularly Sub-Saharan Africa (SSA). The aim of this study is to characterize CPE isolates from patients returning from SSA at both phenotypic and genomic levels. Methods This retrospective study analysed 408 CPE received at the French National Reference Center between 2015 and 2022 and collected from patients returning from SSA. Antibiotic susceptibility testing and WGS were performed to assess phenotypic and genomic diversity. Results Among 408 isolates collected from 29 countries, 55.1% produced oxacillinase-48 (OXA-48)-like carbapenemases, predominantly OXA-181, while 46.3% produced NDM (New Delhi metallo-β-lactamase), with NDM-5 being the major variant despite regional disparities. Temporal analysis revealed a trend shifting from OXA-48-like producers to NDM producers. Ceftazidime-avibactam was effective against 100% of non-metallo-β-lactamase producers. Cefiderocol, amikacin and colistin were effective on 73%, 86.7% and 98.4% of all CPEs respectively. Genomic analysis revealed a polyclonal dissemination among K. pneumoniae strains, whereas three E. coli clonal complexes were dominant (CC410, CC167, CC448). Conclusion This study provides a comprehensive characterization of CPE isolated from patients returning from SSA. WGS allowed the identification of major circulating clones, their associated resistance genes, and their susceptibility to last-resort antibiotics.
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