TY - JOUR
T1 - Machine learning assessment of zoonotic potential in avian influenza viruses using PB2 segment
AU - Kim, Sangwook
AU - Kim, Min Ah
AU - Kim, Bitgoeul
AU - Lee, Jisu
AU - Jung, Se Kyung
AU - Kim, Jonghong
AU - Chung, Ho Young
AU - Lee, Chung Young
AU - Jeong, Sungmoon
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/12
Y1 - 2025/12
N2 - Background: Influenza A virus (IAV) is a major global health threat, causing seasonal epidemics and occasional pandemics. Particularly, Influenza A viruses from avian species pose significant zoonotic threats, with PB2 adaptation serving as a critical first step in cross-species transmission. A comprehensive risk assessment framework based on PB2 sequences is necessary, which should encompass detailed analyses of specific residues and mutations while maintaining sufficient generality for application to non-PB2 segments. Results: In this study, we developed two complementary approaches: a regression-based model for accurately distinguishing among risk groups, and a SHAP-based risk assessment model for more meaningful risk analyses. For the regression-based risk models, we compared various methodologies, including tree ensemble methods, conventional regression models, and deep learning architectures. The optimized regression model, combined with SHAP value analysis, identified and ranked individual residues contributing to zoonotic potential. The SHAP-based risk model enabled intra-class analyses within the zoonotic risk assessment framework and quantified risk yields from specific mutations. Conclusion: Experimental analyses demonstrated that the Random Forest regression model outperformed other models in most cases, and we validated the target value settings for risk regression through ablation studies. Our SHAP-based analysis identified key residues (271A, 627K, 591R, 588A, 292I, 684S, 684A, 81M, 199S, and 368Q) and mutations (T271A, Q368R/K, E627K, Q591R, A588T/I/V, and I292V/T) critical for zoonotic risk assessment. Using the SHAP-based risk assessment model, we found that influenza A viruses from Phasianidae showed elevated zoonotic risk scores compared to those from other avian species. Additionally, mutations I292V/T, Q368R, A588T/I, V598A/I/T, and E/V627K were identified as significant mutations in the Phasianidae. These PB2-focused quantitative methods provide a robust and generalizable framework for both rapid screening of avians’ zoonotic potential and analytical quantification of risks associated with specific residues or mutations.
AB - Background: Influenza A virus (IAV) is a major global health threat, causing seasonal epidemics and occasional pandemics. Particularly, Influenza A viruses from avian species pose significant zoonotic threats, with PB2 adaptation serving as a critical first step in cross-species transmission. A comprehensive risk assessment framework based on PB2 sequences is necessary, which should encompass detailed analyses of specific residues and mutations while maintaining sufficient generality for application to non-PB2 segments. Results: In this study, we developed two complementary approaches: a regression-based model for accurately distinguishing among risk groups, and a SHAP-based risk assessment model for more meaningful risk analyses. For the regression-based risk models, we compared various methodologies, including tree ensemble methods, conventional regression models, and deep learning architectures. The optimized regression model, combined with SHAP value analysis, identified and ranked individual residues contributing to zoonotic potential. The SHAP-based risk model enabled intra-class analyses within the zoonotic risk assessment framework and quantified risk yields from specific mutations. Conclusion: Experimental analyses demonstrated that the Random Forest regression model outperformed other models in most cases, and we validated the target value settings for risk regression through ablation studies. Our SHAP-based analysis identified key residues (271A, 627K, 591R, 588A, 292I, 684S, 684A, 81M, 199S, and 368Q) and mutations (T271A, Q368R/K, E627K, Q591R, A588T/I/V, and I292V/T) critical for zoonotic risk assessment. Using the SHAP-based risk assessment model, we found that influenza A viruses from Phasianidae showed elevated zoonotic risk scores compared to those from other avian species. Additionally, mutations I292V/T, Q368R, A588T/I, V598A/I/T, and E/V627K were identified as significant mutations in the Phasianidae. These PB2-focused quantitative methods provide a robust and generalizable framework for both rapid screening of avians’ zoonotic potential and analytical quantification of risks associated with specific residues or mutations.
KW - Artificial intelligence
KW - Avian influenza virus
KW - Influenza A virus
KW - Machine learning
KW - Mutation analysis
KW - PB2
KW - SHAP
UR - https://www.scopus.com/pages/publications/105003250044
U2 - 10.1186/s12864-025-11589-8
DO - 10.1186/s12864-025-11589-8
M3 - Article
C2 - 40269678
AN - SCOPUS:105003250044
SN - 1471-2164
VL - 26
JO - BMC Genomics
JF - BMC Genomics
IS - 1
M1 - 395
ER -