乌克兰患者中产碳青霉烯酶细菌对最后一种抗生素的抗菌敏感性。

IF 3.7 2区 生物学 Q2 MICROBIOLOGY
Microbiology spectrum Pub Date : 2024-11-05 Epub Date: 2024-09-24 DOI:10.1128/spectrum.01142-24
Nelianne J Verkaik, Cornelia C H Wielders, Hans den Boer, Diana Langerak, Marius Vogel, Sandra Witteveen, Angela de Haan, Jeroen Bos, Mireille van Westreenen, Daan W Notermans, Antoni P A Hendrickx
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引用次数: 0

摘要

自 2022 年 3 月以来,与乌克兰病人转院有关的耐多药微生物(MDRO)有所增加。我们的目标是收集表型药敏数据并评估其临床影响。产碳青霉烯酶肠杆菌(CPE,n = 96)、铜绿假单胞菌(CPPA,n = 20)和耐碳青霉烯类鲍曼不动杆菌-铜绿假单胞菌(CRAB,n = 6)是 2022 年 3 月至 12 月期间从荷兰 MDRO 监测中获得的乌克兰患者的样本。抗菌药敏感性检测采用肉汤微量稀释法(BMD)(如有)、磷霉素琼脂稀释法、头孢菌素盘扩散法(DD)和多样化梯度条带法进行。所有分离物均采用 Illumina 下一代测序技术进行测序。对于美罗培南、氨基糖苷类、头孢唑肟-阿维巴坦、头孢洛氮烷-他唑巴坦和亚胺培南-雷贝拉坦,由于 blaNDM 阳性分离株数量较多(79/122;65%),其药敏率较低(0%-30%)。对于头孢羟氨苄,结果取决于有无微菌落读数、采用 EUCAST 还是 CLSI 断点,以及使用 DD 还是 BMD;例如,对于肺炎克雷伯菌,30%-97% 的菌株对头孢羟氨苄敏感。对于可乐定,103/111 个(93%)非内在耐药的 CPE/CPPA/CRAB 分离物是易感的。对大多数 CPE 而言,最低抑菌浓度(MIC)较低:自 2022 年 3 月以来,欧洲多个国家的国家监测系统发现了与乌克兰患者有关的耐多药微生物。我们研究了荷兰乌克兰患者中的耐多药微生物对最后抗生素的表型抗菌药敏感性,并评估了临床影响。我们的研究发现,最后耐药抗生素存在广泛的表型耐药性。医护人员在治疗近期在乌克兰住院的疑似革兰氏阴性菌感染患者时,应注意耐多药微生物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antimicrobial susceptibility to last-resort antibiotics in carbapenemase-producing bacteria from Ukrainian patients.

Since March 2022, an increase was observed in multidrug-resistant microorganisms (MDRO), associated with the hospital transfer of Ukrainian patients. The goal was to collect phenotypic susceptibility data and assess clinical implications. Carbapenemase-producing Enterobacterales (CPE, n = 96), Pseudomonas aeruginosa (CPPA, n = 20), and carbapenem-resistant Acinetobacter baumannii-calcoaceticus (CRAB, n = 6) from Ukrainian patients were obtained from March to December 2022 from the Dutch MDRO surveillance. Antimicrobial susceptibility testing was performed using broth microdilution (BMD) when available, fosfomycin agar dilution, disk diffusion (DD) for cefiderocol, and diverse gradient strips. All isolates were sequenced with Illumina next-generation sequencing. For meropenem, aminoglycosides, ceftazidime-avibactam, ceftolozane-tazobactam, and imipenem-relebactam, susceptibility rates were low (0%-30%), due to the high number of blaNDM-positive isolates (79/122; 65%). For cefiderocol, results depended on reading with or without microcolonies, applying EUCAST or CLSI breakpoints, and whether DD or BMD was used; e.g., for Klebsiella pneumoniae, 30%-97% were susceptible. For colistin, 103/111 (93%) non-intrinsically resistant CPE/CPPA/CRAB isolates were susceptible. For most CPE, a low minimal inhibitory concentration (MIC) of <0.5 mg/L was measured for tigecycline and ceftazidime-avibactam-aztreonam. For CPPA, cefiderocol tested susceptible in 65%-100% of isolates. For CRAB, ampicillin-sulbactam MICs were ≥128 mg/L; for sulbactam-durlobactam, 1-2 mg/L. Admission in a Ukrainian hospital in the last year was a risk factor for MDRO, and majority were screening isolates (79%). There is extensive phenotypic resistance to last-resort antibiotics in MDRO from Ukrainian patients. Interpretation of cefiderocol susceptibility results depends on several variables. When treating patients recently admitted in Ukraine, suspected for Gram-negative bacterial infection, this should be taken into consideration.

Importance: Since March 2022, multidrug-resistant microorganisms associated with Ukrainian patients have been detected in national surveillance systems of several European countries. We studied the phenotypic antimicrobial susceptibility to last-resort antibiotics of multidrug-resistant microorganisms from Ukrainian patients in the Netherlands and assessed clinical implications. Our research revealed that there was extensive phenotypic resistance to last-resort antibiotics. Healthcare professionals should be aware of multidrug-resistant microorganisms when treating patients recently admitted in Ukraine, suspected for Gram-negative bacterial infection.

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来源期刊
Microbiology spectrum
Microbiology spectrum Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.20
自引率
5.40%
发文量
1800
期刊介绍: Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.
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