Novel, rapid, and reliable typing of vancomycin-resistant Enterococcus faecium CC17/ST80 strains using MALDI-TOF MS.

IF 3.8 2区 生物学 Q2 MICROBIOLOGY
Silke Huber, Christina Brühwasser, David Eisele, Cornelia Lass-Flörl, Stefan Fuchs, Miriam Govrins
{"title":"Novel, rapid, and reliable typing of vancomycin-resistant <i>Enterococcus faecium</i> CC17/ST80 strains using MALDI-TOF MS.","authors":"Silke Huber, Christina Brühwasser, David Eisele, Cornelia Lass-Flörl, Stefan Fuchs, Miriam Govrins","doi":"10.1128/spectrum.02702-25","DOIUrl":null,"url":null,"abstract":"<p><p>Vancomycin-resistant <i>Enterococcus faecium</i> (VREfm) is an important nosocomial pathogen. The recent emergence of the highly virulent clonal complex 17 (CC17) is posing a challenge for both therapeutic interventions and hospital infection control measures. Hence, prompt discrimination of CC17 VREfm from unrelated and less-virulent VREfm strains is essential for preventing its spread in hospitals and beyond. Between January 2022 and November 2024, 340 VREfm primary isolates have been identified in our lab and underwent genotyping by pulsed-field gel electrophoresis (PFGE) to survey a potential outbreak in the Tyrol region. In addition, whole-genome sequencing (WGS) was performed on a selected subset (<i>n</i> = 40). To curtail the lengthy time-to-result (TTR) of these methods, a novel typing protocol using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) was established, validated, and optimized for rapid sample processing. PFGE and WGS showed that 61.2% of isolates (<i>n</i> = 208) belonged to a specific VREfm cluster identified as CC17 sequence type (ST) 80 <i>vanA</i> VREfm. A comprehensive MALDI-TOF MS analysis identified a distinct peak pattern specific to this lineage. This phenotypic characterization was used as a novel typing method with excellent performance (sensitivity: 1.00 [0.98-1.00], specificity: 0.89 [0.70-0.97]) and demonstrated a short TTR of 1 day after the cultural growth of VREfm. A rapid and novel MALDI-TOF MS-based typing approach for a specific CC17/ST80 <i>vanA</i> VREfm cluster was developed and enabled real-life application in routine diagnostics to assure accurate infection prevention and control measures. Future outbreak investigations may benefit from adopting this cost- and labor-efficient approach.IMPORTANCEThis study addresses the urgent need for faster ways to detect problematic hospital bacteria. A highly transmissible strain of <i>Enterococcus faecium</i> (CC17) has been spreading in healthcare settings, making infections harder to treat and control. Traditional methods to identify and track outbreaks are accurate but slow and resource-intensive, delaying critical infection control actions. By developing and validating a new method using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry, the researchers demonstrated that this strain can be identified quickly, reliably, and at lower cost. Importantly, the new approach delivers results within a day, compared to the lengthy turnaround times of existing methods. This rapid detection tool provides hospitals with a practical solution to respond to outbreaks more effectively, prevent further spread, and protect vulnerable patients. The findings highlight a valuable step forward in strengthening hospital infection control and improving patient safety.</p>","PeriodicalId":18670,"journal":{"name":"Microbiology spectrum","volume":" ","pages":"e0270225"},"PeriodicalIF":3.8000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbiology spectrum","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1128/spectrum.02702-25","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Vancomycin-resistant Enterococcus faecium (VREfm) is an important nosocomial pathogen. The recent emergence of the highly virulent clonal complex 17 (CC17) is posing a challenge for both therapeutic interventions and hospital infection control measures. Hence, prompt discrimination of CC17 VREfm from unrelated and less-virulent VREfm strains is essential for preventing its spread in hospitals and beyond. Between January 2022 and November 2024, 340 VREfm primary isolates have been identified in our lab and underwent genotyping by pulsed-field gel electrophoresis (PFGE) to survey a potential outbreak in the Tyrol region. In addition, whole-genome sequencing (WGS) was performed on a selected subset (n = 40). To curtail the lengthy time-to-result (TTR) of these methods, a novel typing protocol using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) was established, validated, and optimized for rapid sample processing. PFGE and WGS showed that 61.2% of isolates (n = 208) belonged to a specific VREfm cluster identified as CC17 sequence type (ST) 80 vanA VREfm. A comprehensive MALDI-TOF MS analysis identified a distinct peak pattern specific to this lineage. This phenotypic characterization was used as a novel typing method with excellent performance (sensitivity: 1.00 [0.98-1.00], specificity: 0.89 [0.70-0.97]) and demonstrated a short TTR of 1 day after the cultural growth of VREfm. A rapid and novel MALDI-TOF MS-based typing approach for a specific CC17/ST80 vanA VREfm cluster was developed and enabled real-life application in routine diagnostics to assure accurate infection prevention and control measures. Future outbreak investigations may benefit from adopting this cost- and labor-efficient approach.IMPORTANCEThis study addresses the urgent need for faster ways to detect problematic hospital bacteria. A highly transmissible strain of Enterococcus faecium (CC17) has been spreading in healthcare settings, making infections harder to treat and control. Traditional methods to identify and track outbreaks are accurate but slow and resource-intensive, delaying critical infection control actions. By developing and validating a new method using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry, the researchers demonstrated that this strain can be identified quickly, reliably, and at lower cost. Importantly, the new approach delivers results within a day, compared to the lengthy turnaround times of existing methods. This rapid detection tool provides hospitals with a practical solution to respond to outbreaks more effectively, prevent further spread, and protect vulnerable patients. The findings highlight a valuable step forward in strengthening hospital infection control and improving patient safety.

新型、快速、可靠的耐万古霉素屎肠球菌CC17/ST80型MALDI-TOF质谱
万古霉素耐药屎肠球菌(VREfm)是一种重要的医院病原菌。最近出现的高毒力克隆复合物17 (CC17)对治疗干预和医院感染控制措施提出了挑战。因此,及时区分CC17 VREfm与不相关且毒性较低的VREfm菌株对于防止其在医院内外传播至关重要。在2022年1月至2024年11月期间,我们的实验室鉴定了340株VREfm初级分离株,并通过脉冲场凝胶电泳(PFGE)进行了基因分型,以调查蒂罗尔地区潜在的疫情。此外,对选定的子集(n = 40)进行全基因组测序(WGS)。为了缩短这些方法的长时间到结果(TTR),建立了一种新的类型协议,使用基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF MS),验证并优化了快速样品处理。PFGE和WGS结果显示,61.2%的分离株(n = 208)属于CC17序列型(ST) 80 vanA VREfm。全面的MALDI-TOF质谱分析鉴定出该谱系特有的明显峰型。这种表型特征被用作一种新的分型方法,具有优异的性能(灵敏度:1.00[0.98-1.00],特异性:0.89[0.70-0.97]),并且在VREfm培养生长后TTR较短,为1天。针对特定的CC17/ST80 vanA VREfm集群,开发了一种快速且新颖的基于MALDI-TOF ms的分型方法,并使其能够在常规诊断中实际应用,以确保准确的感染预防和控制措施。今后的疫情调查可能受益于采用这种成本和劳动效率高的方法。重要意义本研究解决了快速检测医院问题细菌的迫切需求。一种高传染性的屎肠球菌(CC17)一直在卫生保健机构中传播,使感染更难治疗和控制。识别和跟踪疫情的传统方法是准确的,但速度缓慢且资源密集,延误了关键的感染控制行动。通过开发和验证一种使用基质辅助激光解吸/电离飞行时间质谱法的新方法,研究人员证明了这种菌株可以快速、可靠地识别,并且成本更低。重要的是,与现有方法漫长的周转时间相比,新方法可以在一天内交付结果。这种快速检测工具为医院提供了一种实用的解决方案,以更有效地应对疫情,防止进一步传播,并保护脆弱的患者。这一发现为加强医院感染控制和提高患者安全迈出了宝贵的一步。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信