DeepVIC: modular prediction and classification of bacterial virulence factors using protein language model embeddings.

IF 2.6 Q2 MATHEMATICAL & COMPUTATIONAL BIOLOGY
Bioinformatics advances Pub Date : 2026-08-17 eCollection Date: 2026-01-01 DOI:10.1093/bioadv/vbag237
Wai-Kai Tsui, You-Xiang Chan, Kin-Hung Chow, Pak-Leung Ho, Huiluo Cao
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引用次数: 0

Abstract

Motivation: Virulence factors (VFs) play critical roles in bacterial pathogenesis, and identifying these proteins and elucidating their mechanisms is essential for developing effective infection treatments. While protein language models (PLMs) have revolutionized the protein analysis, current in silico methods for classifying VFs primarily rely on fine-tuned PLMs ProtBert-BFD that perform identification and classification in a single step. This monolithic approach lacks flexibility and is vulnerable to error propagation, particularly from false negatives. Moreover, the direct use of PLM embeddings as features for VF prediction and classification remains underexplored.

Results: To overcome these limitations, we introduce the Deep learning VF Identifier and Classifier (DeepVIC), a modular framework that separates identification and classification into distinct states. The identification module employs a binary classifier using information-rich PLM embeddings. The classification module then integrates these embeddings with evolutionary features derived from position-specific scoring matrices (PSSMs) in a multiclass classifier, structured according to the virulence factor database (VFDB) schema. We benchmarked DeepVIC against six state-of-the-art VF classifiers and predictors using a large independent holdout dataset and two literature-curated datasets for Streptococcus pneumoniae and Lactococcus spp. DeepVIC demonstrated strong generalizability, achieving robust and balanced performance on the independent holdout dataset and competitive recall of putative VFs from existing literature. The modular, task-separation architecture adopted in DeepVIC offers exceptional flexibility, making it a uniquely adaptable and competitive framework. Model interpretability strategies reveal that DeepVIC leverages biologically relevant motifs and effectively integrates PLM embeddings with evolutionary features, offering insights into how deep learning models interpret VFs.

DeepVIC:使用蛋白质语言模型嵌入的细菌毒力因子的模块化预测和分类。
动机:毒力因子(VFs)在细菌发病机制中起着关键作用,识别这些蛋白并阐明其机制对于开发有效的感染治疗至关重要。虽然蛋白质语言模型(PLMs)已经彻底改变了蛋白质分析,但目前用于分类VFs的计算机方法主要依赖于微调的PLMs ProtBert-BFD,该方法在一个步骤中执行识别和分类。这种单一的方法缺乏灵活性,容易受到错误传播的影响,特别是假阴性。此外,直接使用PLM嵌入作为VF预测和分类的特征仍未得到充分探索。结果:为了克服这些限制,我们引入了深度学习VF识别器和分类器(DeepVIC),这是一个模块化框架,将识别和分类分离到不同的状态。识别模块采用信息丰富的PLM嵌入的二值分类器。然后,分类模块将这些嵌入与来自特定位置评分矩阵(PSSMs)的进化特征集成到一个多类分类器中,该分类器根据毒力因子数据库(VFDB)模式构建。我们使用一个大型独立抵抗数据集和两个针对肺炎链球菌和乳球菌的文献整理数据集,将DeepVIC与六个最先进的VF分类器和预测器进行基准测试。DeepVIC显示出很强的泛化性,在独立抵抗数据集上实现了稳健和平衡的性能,并从现有文献中竞争性地召回了假定的VF。DeepVIC采用的模块化、任务分离架构提供了卓越的灵活性,使其成为具有独特适应性和竞争力的框架。模型可解释性策略表明,DeepVIC利用了生物学相关的基序,并有效地将PLM嵌入与进化特征集成在一起,为深度学习模型如何解释VFs提供了见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
1.60
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