Mechaly Adva, Vitner Einat B, Levy Yinon, Gur David, Barlev-Gross Moria, Sittner Assa, Koren Michal, Levy Haim, Mamroud Emanuelle, Fisher Morly
The Department of Infectious Diseases, Israel Institute for Biological Research, Ness-Ziona 7410001, Israel.
The Department of Biochemistry and Molecular Genetics, Israel Institute for Biological Research, Ness Ziona 7410001, Israel.
Pathogens. 2021 Mar 2;10(3):285. doi: 10.3390/pathogens10030285.
Mouse monoclonal antibodies were raised against plague disease biomarkers: the bacterial capsular protein fraction 1 (F1) and the low-calcium response-LcrV virulence factor (Vag). A novel tandem assay, employing BioLayer Interferometry (BLI), enabled the isolation of antibodies against four different epitopes on Vag. The tandem assay was carried out with hybridoma supernatants, circumventing the need for antibody purification. The BioLayer assay was further adopted for characterization of epitope-repetitive antigens, enabling the discovery of two unique epitopes on F1. The selected antibodies were purified and applied as "oligo-clonal" reagents for the immuno-detection of both biomarkers. The developed Homogenous Time Resolved Fluorescence (HTRF) tests were short (10 min) and simple (no washing steps), allowing for detection of 10 ng/mL F1 and 2.5 ng/mL Vag. The tests were successfully applied for detection of disease biomarkers produced by various strains during growth in blood culture vials.
细菌荚膜蛋白组分1(F1)和低钙反应LcrV毒力因子(Vag)。一种采用生物层干涉术(BLI)的新型串联检测方法能够分离出针对Vag上四种不同表位的抗体。该串联检测使用杂交瘤细胞上清液进行,无需抗体纯化。生物层检测进一步用于表位重复抗原的表征,从而发现了F1上的两个独特表位。所选抗体经纯化后用作“寡克隆”试剂,用于两种生物标志物的免疫检测。所开发的均相时间分辨荧光(HTRF)检测方法耗时短(10分钟)且操作简单(无需洗涤步骤),能够检测出浓度为10 ng/mL的F1和2.5 ng/mL的Vag。这些检测方法已成功应用于检测血培养瓶中不同菌株生长过程中产生的疾病生物标志物。