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From protein microarrays to diagnostic antigen discovery: a study of the pathogen Francisella tularensis

机译:从蛋白质芯片到诊断性抗原发现:病原菌弗朗西斯菌的研究

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Motivation: An important application of protein microarray data analysis is identifying a serodiagnostic antigen set that can reliably detect patterns and classify antigen expression profiles. This work addresses this problem using antibody responses to protein markers measured by a novel high-throughput microarray technology. The findings from this study have direct relevance to rapid, broad-based diagnostic and vaccine development. Results: Protein microarray chips are probed with sera from individuals infected with the bacteria Francisella tularensis, a category A biodefense pathogen. A two-step approach to the diagnostic process is presented ( 1) feature ( antigen) selection and ( 2) classification using antigen response measurements obtained from F. tularensis microarrays ( 244 antigens, 46 infected and 54 healthy human sera measurements). To select antigens, a ranking scheme based on the identification of significant immune responses and differential expression analysis is described. Classification methods including k-nearest neighbors, support vector machines (SVM) and k-Means clustering are applied to training data using selected antigen sets of various sizes. SVM based models yield prediction accuracy rates in the range of similar to 90% on validation data, when antigen set sizes are between 25 and 50. These results strongly indicate that the top-ranked antigens can be considered high-priority candidates for diagnostic development.
机译:动机:蛋白质微阵列数据分析的一项重要应用是鉴定可以可靠地检测模式并分类抗原表达谱的血清诊断抗原集。这项工作使用通过新型高通量微阵列技术测量的对蛋白质标记物的抗体反应来解决此问题。这项研究的发现与快速,广泛的诊断和疫苗开发直接相关。结果:蛋白微阵列芯片被血清中的细菌弗朗西斯菌Tularensis感染,该细菌是A类生物防御性病原体。提出了一种诊断过程的两步方法(1)使用特征抗原(抗原)选择和(2)使用从杜氏镰刀菌微阵列获得的抗原反应测量值进行分类(244种抗原,46种被感染的人和54种健康的人血清测量)。为了选择抗原,描述了基于显着免疫应答的鉴定和差异表达分析的分级方案。使用选定的各种大小的抗原集,将包括k最近邻,支持向量机(SVM)和k-Means聚类在内的分类方法应用于训练数据。当抗原集大小在25到50之间时,基于SVM的模型在验证数据上的预测准确率约为90%。这些结果强烈表明,排名靠前的抗原可以被认为是诊断开发的高优先级候选者。

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