基质辅助激光解吸/电离飞行时间质谱技术在半乳糖不良链球菌亚群克隆鉴定中的应用equisimilis。

IF 2
Isis Hazelman Vieira Dos Anjos, Caroline Lopes Martini, Luis Guilherme de Araujo Longo, Úrsula Santos Lopez, Tatiana de Castro Abreu Pinto, Agnes Marie Sá Figueiredo, Bernadete Teixeira Ferreira-Carvalho
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引用次数: 0

摘要

介绍。无乳链球菌亚种。equisimilis (SDSE)是一种与化脓性链球菌密切相关的新兴病原体,可引起从轻到重的感染,包括坏死性筋膜炎和中毒性休克综合征。了解细菌多样性对于监测具有抗菌素耐药性和高毒力菌株的传播至关重要。全基因组测序(WGS)克隆分析成本高,耗时长,需要专门的生物信息学专业知识。PFGE定义的克隆通常与人类感染有关,但PFGE也要求很高,成本很高,不同实验室的结果也不尽相同。本研究探索了利用基质辅助激光解吸/电离飞行时间质谱(MALDI-TOF MS)检测具有不同PFGE克隆类型的SDSE菌株的特异性生物标志物。使用Microflex LT质谱仪(Bruker)生成SDSE菌株的MALDI-TOF质谱,并使用BioNumerics软件v7.6进行分析。为了验证PFGE脉冲型的遗传相关性,进行了WGS和系统基因组重建。独特的MALDI-TOF MS生物标记峰一致地区分了PFGE模式A和B对应的SDSE菌株,为区分这些克隆类型提供了强大的分子特征。系统基因组学分析进一步支持了这一区别,将PFGE A和B菌株聚类为两个不同的主分支,准确率提高到95.2(95%置信区间:76.2-99.9%)。MALDI-TOF质谱不仅能有效地进行物种鉴定,而且能快速、可靠地评估SDSE克隆多样性。该方法有可能实现对特定克隆的流行病学跟踪,增强对人类感染中SDSE的了解,并为研究和临床监测提供实用工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Matrix-assisted laser desorption/ionization-time of flight MS as a tool for clonal discrimination in Streptococcus dysgalactiae subsp. equisimilis.

Introduction. Streptococcus dysgalactiae subsp. equisimilis (SDSE) is an emerging pathogen closely related to Streptococcus pyogenes, causing infections from mild to severe, including necrotizing fasciitis and toxic shock syndrome. Understanding bacterial diversity is crucial for monitoring the spread of antimicrobial-resistant and highly virulent strains. Clonal analysis by whole-genome sequencing (WGS) is costly, time-consuming and requires specialized bioinformatics expertise. PFGE-defined clones are often linked to human infections, but PFGE is also demanding and costly and results can vary between laboratories.Aim. This study explores the use of matrix-assisted laser desorption/ionization-time of flight MS (MALDI-TOF MS) to detect discriminatory biomarkers that discriminate SDSE strains exhibiting distinct PFGE clonal types.Methodology. MALDI-TOF MS spectra were generated from SDSE strains using a Microflex LT mass spectrometer (Bruker) and analysed with BioNumerics software v7.6. To validate the genetic relevance of PFGE pulsotypes, WGS and phylogenomic reconstruction were performed.Results. Unique MALDI-TOF MS biomarker peaks consistently differentiated SDSE strains corresponding to PFGE patterns A and B, providing robust molecular signatures for discriminating these clonal types. Phylogenomic analyses further supported this distinction by clustering PFGE A and B strains into two distinct main clades with an elevated accuracy of 95.2 (95% confidence interval: 76.2-99.9%).Conclusion. MALDI-TOF MS is effective not only for species identification but also for rapid and reliable assessment of SDSE clonal diversity. This approach has the potential to enable epidemiological tracking of specific clones, enhance understanding of SDSE in human infections and provide a practical tool for research and clinical surveillance.

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