Prado-Prado Francisco J, González-Díaz Humberto, Santana Lourdes, Uriarte Eugenio
Department of Organic Chemistry and Institute of Industrial Pharmacy, Faculty of Pharmacy, University of Santiago de Compostela, 15782 Santiago, Spain.
Bioorg Med Chem. 2007 Jan 15;15(2):897-902. doi: 10.1016/j.bmc.2006.10.039. Epub 2006 Oct 21.
There are many different kinds of pathogenic bacteria species with very different susceptibility profiles to different antibacterial drugs. One limitation of QSAR models is that they consider the biological activity of drugs against only one species of bacteria. In a previous paper, we developed a unified Markov model to describe the biological activity of different drugs tested in the literature against some antimicrobial species. Consequently, predicting the probability with which a drug is active against different species of bacteria with a single unified model is a goal of major importance. The work described here develops the unified Markov model to describe the biological activity of more than 70 drugs from the literature tested against 96 species of bacteria. We applied linear discriminant analysis (LDA) to classify drugs as active or inactive against the different tested bacterial species. The model correctly classified 199 out of 237 active compounds (83.9%) and 168 out of 200 inactive compounds (84%). Overall training predictability was 84% (367 out of 437 cases). Validation of the model was carried out using an external predicting series, with the model classifying 202 out of 243 (i.e., 83.13%) of the compounds. In order to show how the model functions in practice, a virtual screening was carried out and the model recognized as active 84.5% (480 out of 568) antibacterial compounds not used in the training or predicting series. The current study is an attempt to calculate within a unified framework the probabilities of antibacterial action of drugs against many different species.
存在许多不同种类的致病细菌,它们对不同抗菌药物的敏感性差异很大。定量构效关系(QSAR)模型的一个局限性在于,它们仅考虑药物针对单一细菌物种的生物活性。在之前的一篇论文中,我们开发了一个统一的马尔可夫模型,以描述文献中测试的不同药物对某些抗菌物种的生物活性。因此,用一个统一的模型预测一种药物对不同细菌物种具有活性的概率是一个非常重要的目标。本文所述的工作进一步发展了统一的马尔可夫模型,以描述文献中70多种药物针对96种细菌的生物活性。我们应用线性判别分析(LDA)将药物分类为对不同测试细菌物种有活性或无活性。该模型正确分类了237种活性化合物中的199种(83.9%)和200种无活性化合物中的168种(84%)。总体训练可预测性为84%(437例中的367例)。使用外部预测系列对模型进行验证,该模型对243种化合物中的202种(即83.13%)进行了分类。为了展示该模型在实际中的作用,进行了虚拟筛选,该模型识别出84.5%(568种中的480种)未用于训练或预测系列的抗菌化合物具有活性。当前的研究试图在一个统一的框架内计算药物对许多不同物种的抗菌作用概率。