HViLM: A Foundation Model for Viral Genomics Enables Multi-Task Prediction of Pathogenicity, Transmissibility, and Host Tropism

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Abstract

Motivation The emergence of novel viral pathogens poses critical threats to global health, yet current computational approaches for viral risk assessment are predominantly virus-specific and require extensive retraining for each new threat. Computational methods for rapid characterization of emerging viruses across multiple epidemiologically relevant dimensions—pathogenicity, host tropism, and transmissibility—are urgently needed to inform public health responses and guide experimental prioritization. Results We present HViLM (Human Virome Language Model) , the first foundation model for panviral genomic analysis through continued pre-training of DNABERT-2 on 5 million non-redundant viral sequences (MMseqs2-clustered from 25 million chunks at 80% identity) spanning 9,000 species across 45+ viral families from the VIRION database. We introduce the Human Virome Understanding Evaluation (HVUE) benchmark comprising seven curated datasets across three prediction tasks: pathogenicity classification, host tropism prediction, and transmissibility assessment. Through parameter-efficient fine-tuning with LoRA, HViLM achieves state-of-the-art performance with average accuracies of 95.32% for pathogenicity, 96.25% for host tropism, and 97.36% for transmissibility assessment. The model demonstrates robust cross-family generalization, substantially outperforming sequence-similarity baselines and general genomic foundation models. Attention-based interpretability analysis reveals that HViLM captures biologically meaningful pathogenicity determinants through molecular mimicry of host regulatory elements, including convergent evolution of eight independent sequences targeting Interferon Regulatory Factor 1 (Irf1) for immune evasion. Availability The HVUE benchmark datasets, training scripts, and complete implementation are publicly available at https://github.com/duttaprat/HViLM . Pre-trained HViLM-base model weights and fine-tuned task-specific variants are available on Hugging Face at https://huggingface.co/duttaprat/HViLM-base . Supplementary information Supplementary data are available online.
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Abstract

Motivation The emergence of novel viral pathogens poses critical threats to global health, yet current computational approaches for viral risk assessment are predominantly virus-specific and require extensive retraining for each new threat. Computational methods for rapid characterization of emerging viruses across multiple epidemiologically relevant dimensions—pathogenicity, host tropism, and transmissibility—are urgently needed to inform public health responses and guide experimental prioritization.

Results

We present HViLM (Human Virome Language Model), the first foundation model for panviral genomic analysis through continued pre-training of DNABERT-2 on 5 million non-redundant viral sequences (MMseqs2-clustered from 25 million chunks at 80% identity) spanning 9,000 species across 45+ viral families from the VIRION database. We introduce the Human Virome Understanding Evaluation (HVUE) benchmark comprising seven curated datasets across three prediction tasks: pathogenicity classification, host tropism prediction, and transmissibility assessment. Through parameter-efficient fine-tuning with LoRA, HViLM achieves state-of-the-art performance with average accuracies of 95.32% for pathogenicity, 96.25% for host tropism, and 97.36% for transmissibility assessment. The model demonstrates robust cross-family generalization, substantially outperforming sequence-similarity baselines and general genomic foundation models. Attention-based interpretability analysis reveals that HViLM captures biologically meaningful pathogenicity determinants through molecular mimicry of host regulatory elements, including convergent evolution of eight independent sequences targeting Interferon Regulatory Factor 1 (Irf1) for immune evasion. Availability The HVUE benchmark datasets, training scripts, and complete implementation are publicly available at https://github.com/duttaprat/HViLM. Pre-trained HViLM-base model weights and fine-tuned task-specific variants are available on Hugging Face at https://huggingface.co/duttaprat/HViLM-base. Supplementary information Supplementary data are available online.

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