College of Computer Science and Technology, Hengyang Normal University, Hengyang, 421010, China.
Institute of Bioinformatics Complex Network Big Data, Changsha University, Changsha, 410022, China.
Sci Rep. 2023 May 6;13(1):7396. doi: 10.1038/s41598-023-34438-8.
Microbes are intimately tied to the occurrence of various diseases that cause serious hazards to human health, and play an essential role in drug discovery, clinical application, and drug quality control. In this manuscript, we put forward a novel prediction model named MDASAE based on a stacked autoencoder (SAE) with multi-head attention mechanism to infer potential microbe-drug associations. In MDASAE, we first constructed three kinds of microbe-related and drug-related similarity matrices based on known microbe-disease-drug associations respectively. And then, we fed two kinds of microbe-related and drug-related similarity matrices respectively into the SAE to learn node attribute features, and introduced a multi-head attention mechanism into the output layer of the SAE to enhance feature extraction. Thereafter, we further adopted the remaining microbe and drug similarity matrices to derive inter-node features by using the Restart Random Walk algorithm. After that, the node attribute features and inter-node features of microbes and drugs would be fused together to predict scores of possible associations between microbes and drugs. Finally, intensive comparison experiments and case studies based on different well-known public databases under 5-fold cross-validation and 10-fold cross-validation respectively, proved that MDASAE can effectively predict the potential microbe-drug associations.
微生物与各种疾病的发生密切相关,这些疾病对人类健康造成严重危害,在药物发现、临床应用和药物质量控制中发挥着重要作用。在本文中,我们提出了一种名为 MDASAE 的新型预测模型,该模型基于具有多头注意力机制的堆叠自编码器 (SAE) 来推断潜在的微生物-药物关联。在 MDASAE 中,我们首先基于已知的微生物-疾病-药物关联分别构建了三种微生物相关和药物相关的相似性矩阵。然后,我们将两种微生物相关和药物相关的相似性矩阵分别输入 SAE 以学习节点属性特征,并在 SAE 的输出层引入多头注意力机制来增强特征提取。此后,我们进一步采用剩余的微生物和药物相似性矩阵,通过重新启动随机游走算法,推导出节点间特征。然后,将微生物和药物的节点属性特征和节点间特征融合在一起,以预测微生物和药物之间可能存在的关联的评分。最后,通过基于不同知名公共数据库的 5 倍交叉验证和 10 倍交叉验证的大量比较实验和案例研究,证明 MDASAE 可以有效地预测潜在的微生物-药物关联。