National Research Laboratory of Molecular Biotechnology, Department of Chemical Engineering, Pohang University of Science and Technology, Pohang 790-784, Korea.
Biotechnol Bioeng. 2010 Jun 1;106(2):183-92. doi: 10.1002/bit.22674.
Pathogen detection is an important issue in human health due to the threats posed by severe communicable diseases. In the present study, to achieve efficient and accurate multiple detection of 11 selected pathogenic bacteria, we constructed a 16S rDNA oligonucleotide microarray containing doubly specific capture probes. Many target pathogens were specifically detected by the microarray with the aid of traditional perfect match-based analysis using our previously proposed two-dimensional visualization plot tool. However, some target species or subtypes were difficult to discriminate by perfect match analysis due to nonspecific binding of conserved 16S rDNA-derived capture probes with high sequence similarity. We noticed that the patterns of specific spots for each strain were somewhat different in the two-dimensional gradation plot. Therefore, to discriminate subtle differences between phylogenetically related pathogens, a pattern-mapping statistical model was established using an artificial neural network algorithm trained by experimental repeats. The oligonucleotide microarray system harboring doubly specific capture probes combined with the pattern-mapping analysis tool resulted in successful detection of all target pathogens including even subtypes of two closely related species showing strong nonspecific binding. Collectively, the results indicate that our novel combined system of a 16S rDNA-based DNA microarray and a pattern-mapping statistical analysis tool is a simple and effective method for detecting multiple pathogens.
病原体检测在人类健康中是一个重要的问题,因为严重的传染病会带来威胁。在本研究中,为了实现对 11 种选定的致病细菌的高效、准确的多重检测,我们构建了一个包含双重特异性捕获探针的 16S rDNA 寡核苷酸微阵列。借助我们之前提出的二维可视化绘图工具的传统完美匹配分析,微阵列可以特异性地检测到许多目标病原体。然而,由于具有高度序列相似性的保守 16S rDNA 衍生捕获探针的非特异性结合,一些目标物种或亚型难以通过完美匹配分析来区分。我们注意到,每个菌株的特异性斑点在二维梯度图中的模式有些不同。因此,为了区分系统发育上相关的病原体之间的细微差异,我们使用通过实验重复训练的人工神经网络算法建立了一种模式映射统计模型。包含双重特异性捕获探针的寡核苷酸微阵列系统与模式映射分析工具相结合,成功地检测到了所有的目标病原体,包括两个密切相关的物种的亚型,尽管它们具有强烈的非特异性结合。总的来说,这些结果表明,我们基于 16S rDNA 的 DNA 微阵列和模式映射统计分析工具的新型组合系统是一种简单有效的多重病原体检测方法。