A predictive language model for SARS-CoV-2 evolution

Modeling and predicting mutations are critical for COVID-19 and similar pandemic preparedness. However, existing predictive models have yet to integrate the regularity and randomness of viral mutations with minimal data requirements. Here, we develop a non-demanding language model utilizing both regularity and randomness to predict candidate SARS-CoV-2 variants and mutations that might prevail. We constructed the "grammatical frameworks" of the available S1 sequences for dimension reduction and semantic representation to grasp the model's latent regularity. The mutational profile, defined as the frequency of mutations, was introduced into the model to incorporate randomness. With this model, we successfully identified and validated several variants with significantly enhanced viral infectivity and immune evasion by wet-lab experiments. By inputting the sequence data from three different time points, we detected circulating strains or vital mutations for XBB.1.16, EG.5, JN.1, and BA.2.86 strains before their emergence. In addition, our results also predicted the previously unknown variants that may cause future epidemics. With both the data validation and experiment evidence, our study represents a fast-responding, concise, and promising language model, potentially generalizable to other viral pathogens, to forecast viral evolution and detect crucial hot mutation spots, thus warning the emerging variants that might raise public health concern.

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Publication Details

Journal
Signal Transduction and Targeted Therapy
Published
2024-12-22
DOI
https://doi.org/10.1038/s41392-024-02066-x
Citations
10
Primary Topic
SARS-CoV-2 and COVID-19 Research
Type
article
Field-Weighted Citation Impact
3.89

Funders

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article

A predictive language model for SARS-CoV-2 evolution

Penghua Wang, Xuan Guo, Enhao Ma, Gong Cheng et al.
10 citations
Signal Transduction and Targeted Therapy
SARS-CoV-2 and COVID-19 Research
3.89
article

A predictive language model for SARS-CoV-2 evolution

Penghua Wang, Xuan Guo, Enhao Ma, Gong Cheng, Mingda Hu, Congwen Wei, Xin Wang
article en
10 citations

Abstract

Modeling and predicting mutations are critical for COVID-19 and similar pandemic preparedness. However, existing predictive models have yet to integrate the regularity and randomness of viral mutations with minimal data requirements. Here, we develop a non-demanding language model utilizing both regularity and randomness to predict candidate SARS-CoV-2 variants and mutations that might prevail. We constructed the "grammatical frameworks" of the available S1 sequences for dimension reduction and semantic representation to grasp the model's latent regularity. The mutational profile, defined as the frequency of mutations, was introduced into the model to incorporate randomness. With this model, we successfully identified and validated several variants with significantly enhanced viral infectivity and immune evasion by wet-lab experiments. By inputting the sequence data from three different time points, we detected circulating strains or vital mutations for XBB.1.16, EG.5, JN.1, and BA.2.86 strains before their emergence. In addition, our results also predicted the previously unknown variants that may cause future epidemics. With both the data validation and experiment evidence, our study represents a fast-responding, concise, and promising language model, potentially generalizable to other viral pathogens, to forecast viral evolution and detect crucial hot mutation spots, thus warning the emerging variants that might raise public health concern.

Signal Transduction and Targeted TherapyVol. 9(1)
Shenzhen Bay Laboratory (CN), Beijing Fengtai Hospital (CN), UConn Health (US), Tsinghua University (CN)
Tencent, National Natural Science Foundation of China, Tsinghua University
Good health and well-being
Openalex Percentile: Top 5%
SARS-CoV-2 and COVID-19 Research
3.89
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