{"title":"Rapid Identification of Pathogenic Bacteria from Clinic Positive Blood Cultures Via Virus-like Magnetic Bead Enrichment and MALDI-TOF MS Profiling","authors":"Zhirou Zhang, Enyun Xing, Wenzhuo Zhao, Minghui Song, Cuiping Zhang, Hong Liu, Xiaomin Li, Hongxiu Yu","doi":"10.1039/d4an01424c","DOIUrl":null,"url":null,"abstract":"Reducing the time required for the detection of bacteria in blood samples is a critical area of investigation in the field of clinical diagnosis. Positive blood culture samples often require a plate culture stage due to the interference of blood cells and proteins, which can result in significant delays before the isolation of single colonies suitable for matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) analysis. In this study, we developed a non-specific enrichment strategy based on SiO<small><sub>2</sub></small>-encapsulated Fe<small><sub>3</sub></small>O<small><sub>4</sub></small> nanoparticles combined with MALDI-TOF MS for direct identification of bacteria from aqueous environments or positive blood culture samples. Three distinct types of Fe<small><sub>3</sub></small>O<small><sub>4</sub></small>@SiO<small><sub>2</sub></small> magnetic nanoparticles (MNPs) with unique surface morphologies were developed: spherical MNPs with smooth surfaces (Fe<small><sub>3</sub></small>O<small><sub>4</sub></small>@SN), mesoporous silica coated MNPs (Fe<small><sub>3</sub></small>O<small><sub>4</sub></small>@MSN), and MNPs exhibiting a viral spiked structure (Fe<small><sub>3</sub></small>O<small><sub>4</sub></small>@VSN). These MNPs exhibited excellent binding affinity towards both <em>Staphylococcus aureus</em> and <em>Klebsiella pneumoniae</em> in PBS and artificial saliva solutions. Furthermore, the use of the Fe<small><sub>3</sub></small>O<small><sub>4</sub></small>@VSN strategy, which involves non-specific interactions between bacterial cells and the virus-like surface, resulted in a dramatic reduction in the minimum detectable concentrations of target pathogens by up to 1000-fold compared to conventional methods. Our results demonstrate that the Fe<small><sub>3</sub></small>O<small><sub>4</sub></small>@VSN strategy has the potential to significantly reduce the processing time required after blood culture and may be useful for enrichment and identification of microorganisms in complex clinical samples.","PeriodicalId":63,"journal":{"name":"Analyst","volume":"36 1","pages":""},"PeriodicalIF":3.6000,"publicationDate":"2025-01-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analyst","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d4an01424c","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Reducing the time required for the detection of bacteria in blood samples is a critical area of investigation in the field of clinical diagnosis. Positive blood culture samples often require a plate culture stage due to the interference of blood cells and proteins, which can result in significant delays before the isolation of single colonies suitable for matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) analysis. In this study, we developed a non-specific enrichment strategy based on SiO2-encapsulated Fe3O4 nanoparticles combined with MALDI-TOF MS for direct identification of bacteria from aqueous environments or positive blood culture samples. Three distinct types of Fe3O4@SiO2 magnetic nanoparticles (MNPs) with unique surface morphologies were developed: spherical MNPs with smooth surfaces (Fe3O4@SN), mesoporous silica coated MNPs (Fe3O4@MSN), and MNPs exhibiting a viral spiked structure (Fe3O4@VSN). These MNPs exhibited excellent binding affinity towards both Staphylococcus aureus and Klebsiella pneumoniae in PBS and artificial saliva solutions. Furthermore, the use of the Fe3O4@VSN strategy, which involves non-specific interactions between bacterial cells and the virus-like surface, resulted in a dramatic reduction in the minimum detectable concentrations of target pathogens by up to 1000-fold compared to conventional methods. Our results demonstrate that the Fe3O4@VSN strategy has the potential to significantly reduce the processing time required after blood culture and may be useful for enrichment and identification of microorganisms in complex clinical samples.