Dan Liu, Francesca Young, Kieran D Lamb, David L Robertson, Ke Yuan
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引用次数: 0
摘要
预测病毒与宿主的关联对于确定病毒与之相互作用的特定宿主物种以及发现新病毒是否会感染人类和动物至关重要。目前,大多数病毒的宿主都是未知的,尤其是在微生物组中。为了应对这一挑战,我们引入了 EvoMIL,这是一种仅从病毒序列预测病毒宿主物种的深度学习方法。它还能识别对宿主预测有重大贡献的重要病毒蛋白。该方法结合了预先训练的大型蛋白质语言模型(ESM)和基于注意力的多实例学习,从而实现了面向蛋白质的预测。我们的研究结果表明,与氨基酸、理化性质和 DNA k-mers 等序列组成特征相比,蛋白质嵌入能捕捉到更强的预测信号。在多宿主预测任务中,EvoMIL 对原核宿主的中位 F1 分数分别提高了 10.8%、16.2% 和 4.9%,对真核宿主的中位 F1 分数分别提高了 1.7%、6.6% 和 11.5%。EvoMIL 的二元分类器在所有原核宿主中的 AUC 都超过了 0.95,令人印象深刻;在真核宿主中,AUC 大约在 0.8 到 0.9 之间。此外,EvoMIL 还能识别预测任务中的重要蛋白质。我们发现它们捕捉到了病毒-宿主特异性的关键功能。
Prediction of virus-host associations using protein language models and multiple instance learning.
Predicting virus-host associations is essential to determine the specific host species that viruses interact with, and discover if new viruses infect humans and animals. Currently, the host of the majority of viruses is unknown, particularly in microbiomes. To address this challenge, we introduce EvoMIL, a deep learning method that predicts the host species for viruses from viral sequences only. It also identifies important viral proteins that significantly contribute to host prediction. The method combines a pre-trained large protein language model (ESM) and attention-based multiple instance learning to allow protein-orientated predictions. Our results show that protein embeddings capture stronger predictive signals than sequence composition features, including amino acids, physiochemical properties, and DNA k-mers. In multi-host prediction tasks, EvoMIL achieves median F1 score improvements of 10.8%, 16.2%, and 4.9% in prokaryotic hosts, and 1.7%, 6.6% and 11.5% in eukaryotic hosts. EvoMIL binary classifiers achieve impressive AUC over 0.95 for all prokaryotic hosts and range from roughly 0.8 to 0.9 for eukaryotic hosts. Furthermore, EvoMIL identifies important proteins in the prediction task. We found them capturing key functions in virus-host specificity.
期刊介绍:
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