Shifting molecular epidemiology of carbapenem-resistant Klebsiella pneumoniae in a regional Greek hospital: Department-specific trends and national context (2022-2024).

IF 1.6 4区 医学 Q4 IMMUNOLOGY
Acta microbiologica et immunologica Hungarica Pub Date : 2025-07-17 Print Date: 2025-10-09 DOI:10.1556/030.2025.02655
Pandora Tsolakidou, Georgios Tsikrikonis, Kontantina Tsaprouni, Martha Souplioti, Eumorfia Sxoina
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引用次数: 0

Abstract

Carbapenem-resistant Klebsiella pneumoniae (CRKP) poses a growing threat in Greek hospitals, with increasing reports of multidrug- and pandrug-resistant strains; however, molecular data from regional centers remain limited. This study aimed to investigate the molecular epidemiology, resistance mechanisms, and transmission dynamics of CRKP isolates collected at the General Hospital of Volos, Central Greece, between 2022 and 2024. Thirty-seven non-duplicate CRKP isolates were analyzed. Identification and antibiotic susceptibility testing were performed using VITEK® 2, disk diffusion, Etest®, and broth microdilution. Carbapenemase production was assessed using the NG-Test® Carba-5. Eight isolates underwent multilocus sequence typing (MLST). All isolates were resistant to carbapenems, cephalosporins, and fluoroquinolones; furthermore, 40% were colistin-resistant. The dominant carbapenemase genes were blaNDM-1 (45.9%), blaKPC-2 (18.9%), and blaVIM-1 (27.0%), with co-expression of multiple carbapenemases in 30% of the isolates. MLST revealed the high-risk clones ST11, ST15, and ST323, and three intra-intensive care unit (ICU) transmission clusters. The emergence of dual-carbapenemase and colistin-resistant clones underscores the need for local genomic surveillance, improved infection control, and access to newer antimicrobials in non-tertiary settings.

希腊一家地区医院耐碳青霉烯肺炎克雷伯菌的分子流行病学变化:部门特定趋势和国家背景(2022-2024)。
耐碳青霉烯肺炎克雷伯菌(CRKP)在希腊医院构成越来越大的威胁,越来越多的多药和泛药耐药菌株的报告;然而,来自区域中心的分子数据仍然有限。本研究旨在调查2022年至2024年在希腊中部Volos总医院收集的CRKP分离株的分子流行病学、耐药机制和传播动力学。分析了37株非重复的CRKP分离株。使用VITEK®2、纸片扩散、Etest®和肉汤微量稀释进行鉴定和药敏试验。使用NG-Test®Carba-5评估碳青霉烯酶的产生。8株进行了多位点序列分型(MLST)。所有分离株均对碳青霉烯类、头孢菌素类和氟喹诺酮类耐药;此外,40%的患者对粘菌素耐药。碳青霉烯酶基因主要为blaNDM-1(45.9%)、blaKPC-2(18.9%)和blaVIM-1(27.0%),其中30%的菌株存在多种碳青霉烯酶共表达。MLST发现高危克隆ST11、ST15和ST323,以及3个重症监护病房(ICU)内传播聚集群。双碳青霉烯酶和粘菌素耐药克隆的出现强调了在非三级环境中进行局部基因组监测、改进感染控制和获得更新的抗菌素的必要性。
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
2.30
自引率
13.30%
发文量
36
审稿时长
>12 weeks
期刊介绍: AMIH is devoted to the publication of research in all fields of medical microbiology (bacteriology, virology, parasitology, mycology); immunology of infectious diseases and study of the microbiome related to human diseases.
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