Immunoassay-mass spectrometry to identify Brucella melitensis.

IF 4.8 2区 医学 Q2 IMMUNOLOGY Frontiers in Cellular and Infection Microbiology Pub Date : 2025-02-04 eCollection Date: 2025-01-01 DOI:10.3389/fcimb.2025.1531018
Amirreza Sharif, Ramin Bagheri Nejad, Alireza Ghassempour
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Abstract

Two factors frequently impede accurate bacterial identification using matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS): inadequate bacterial abundance in real samples and bacterial combinations. For MALDI-TOF MS analysis and libraries for bacterial identification, time-consuming culture procedures are necessary to achieve sufficient concentration and isolation of a single bacterium. When dealing with hazardous bacteria like Brucella, which are more difficult to handle and cure, this problem becomes even more crucial. To overcome these obstacles, Fe3O4 magnetic nanoparticles (MNPs) linked with Brucella-specific antibodies and MALDI-TOF MS analysis have been used to create a quick and accurate technique for direct bacterial separation and identification in complex samples. This method allows MNPs to immune-selectively collect Brucella cells, which are then deactivated and ready for MALDI-TOF MS analysis by a formic acid/acetonitrile wash. Rabbits were used to manufacture brucella antibodies, which have effectively adsorbed onto the MNPs-protein A. Any particular Brucella bacteria found in the media might be absorbed by this MNPs-protein A-antibody immunoprobe. The concentration of Brucella bacterial cells increases the protein spectrum's visibility by a factor of 103, making it possible to quickly identify Brucella spp. without first growing them in cultural conditions. This method has been successfully used to achieve a limit of detection (LOD) of 50 CFU/mL in an aqueous medium and genuine sample-milk. The diagnostic time for this harmful bacterium is greatly decreased because the entire procedure from bacterial isolation to species identification is finished in less than 60 min. High sensitivity and specificity are demonstrated by the immunoassay-MS approach, as the spectral pattern it produces matches well-known databases like SPECLUST and Ribopeaks.

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免疫测定-质谱法鉴定梅利氏布鲁氏菌。
两个因素经常阻碍使用基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)进行准确的细菌鉴定:实际样品中的细菌丰度不足和细菌组合。对于用于细菌鉴定的MALDI-TOF MS分析和文库,需要耗时的培养程序才能达到足够的浓度和分离单个细菌。在处理像布鲁氏菌这样更难处理和治愈的危险细菌时,这个问题变得更加关键。为了克服这些障碍,利用Fe3O4磁性纳米颗粒(MNPs)结合布鲁氏菌特异性抗体和MALDI-TOF质谱分析,建立了一种快速准确的技术,用于复杂样品的直接细菌分离和鉴定。该方法允许MNPs免疫选择性地收集布鲁氏菌细胞,然后将其灭活并准备通过甲酸/乙腈洗涤进行MALDI-TOF MS分析。兔制备的布氏菌抗体能有效吸附在mnps -蛋白a上。培养基中发现的任何特定的布氏菌均可被mnps -蛋白a抗体免疫探针所吸附。布鲁氏菌细胞的浓度将蛋白质光谱的可见度提高了103倍,使得无需首先在培养条件下培养就可以快速识别布鲁氏菌。该方法在含水介质和正品牛奶中的检出限(LOD)为50 CFU/mL。这种有害细菌的诊断时间大大缩短,因为从细菌分离到物种鉴定的整个过程在不到60分钟内完成。免疫测定-质谱法显示出高灵敏度和特异性,因为它产生的光谱模式与SPECLUST和Ribopeaks等知名数据库相匹配。
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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
1817
审稿时长
14 weeks
期刊介绍: Frontiers in Cellular and Infection Microbiology is a leading specialty journal, publishing rigorously peer-reviewed research across all pathogenic microorganisms and their interaction with their hosts. Chief Editor Yousef Abu Kwaik, University of Louisville is supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Cellular and Infection Microbiology includes research on bacteria, fungi, parasites, viruses, endosymbionts, prions and all microbial pathogens as well as the microbiota and its effect on health and disease in various hosts. The research approaches include molecular microbiology, cellular microbiology, gene regulation, proteomics, signal transduction, pathogenic evolution, genomics, structural biology, and virulence factors as well as model hosts. Areas of research to counteract infectious agents by the host include the host innate and adaptive immune responses as well as metabolic restrictions to various pathogenic microorganisms, vaccine design and development against various pathogenic microorganisms, and the mechanisms of antibiotic resistance and its countermeasures.
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