Machine learning-driven identification of immune signatures from RNA-Seq data in H5N1-infected chickens: a computational Immunology approach

Authors

    Fatemeh Keivan Department of Microbiology and Immunology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran.
    Gholamreza Nikbakht Brujeni * Department of Microbiology and Immunology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran. nikbakht@ut.ac.ir

Keywords:

H5N1, RNA-Seq, Machine Learning (ML), Chicken immune response, Immunoinformatics.

Abstract

Highly Pathogenic Avian Influenza (H5N1) continues to pose a serious risk to public health and poultry. In order to differentiate H5N1-infected from healthy chicken samples and to guide the development of diagnostics and vaccines, we postulated that Machine Learning (ML) applied to RNA sequencing (RNA-Seq) data could biologically detect meaningful immune gene signatures. While previous transcriptomic studies have characterized host responses to H5N1 infection in chickens, the application of interpretable machine-learning approaches to prioritize immune-associated transcriptional signatures from chicken RNA-Seq datasets remains relatively unexplored. RNA-Seq data from H5N1-infected chicken lung and ileum tissues (ArrayExpress E-MTAB-2908) that were publicly available, were chosen. Fivefold stratified cross-validation (~80/20 train/test per fold) was used to train two supervised ML models, such as Random Forest (RF) and linear-kernel Support Vector Machine (SVM). Performance was evaluated using Area Under Curve (AUC) and Receiver Operating Characteristic (ROC) curves.  RF reached a mean AUC=0.85, while SVM-Linear achieved AUC=0.75. Top-ranking interferon-stimulated genes (ISGs), including IFIT5, MX1, and OASL, were consistently upregulated in infected samples, indicating activation of type I interferon pathways. Concordant findings across models support the stability and biological relevance of the identified signatures despite the modest sample size. These findings demonstrate that interpretable ML approaches can successfully prioritize biologically relevant antiviral signatures from chicken RNA-Seq datasets. However, the identified signatures should be considered candidate computational immune signatures that require independent experimental validation before potential application in biomarker development, disease surveillance, or vaccine-related research.

Downloads

Download data is not yet available.

References

Ahmed, N., Ranaware, P. B., Mishra, A., Vijayakumar, P., Gandhale, P. N., Kumar, H., Kulkarni, D. D., & Raut, A. A. (2016). Genome Wide Host Gene Expression Analysis in Chicken Lungs Infected with Avian Influenza Viruses. Plos One, 11(4). https://doi.org/10.1371/journal.pone.0153671

Breiman, L. (2001). . Machine Learning, 45(1). https://doi.org/https://doi.org/10.1023/A:1010933404324

Bzhalava, Z., Tampuu, A., Bala, P., Vicente, R., & Dillner, J. (2018). Machine Learning for detection of viral sequences in human metagenomic datasets. BMC Bioinformatics, 19(1), 336. https://doi.org/10.1186/s12859-018-2340-x

Ching, T., Himmelstein, D. S., Beaulieu-Jones, B. K., Kalinin, A. A., Do, B. T., Way, G. P., Ferrero, E., Agapow, P. M., Zietz, M., Hoffman, M. M., Xie, W., Rosen, G. L., Lengerich, B. J., Israeli, J., Lanchantin, J., Woloszynek, S., Carpenter, A. E., Shrikumar, A., Xu, J., . . . Greene, C. S. (2018). Opportunities and obstacles for deep learning in biology and medicine. J R Soc Interface, 15(141). https://doi.org/10.1098/rsif.2017.0387

Conesa, A., Madrigal, P., Tarazona, S., Gomez-Cabrero, D., Cervera, A., McPherson, A., Szczesniak, M. W., Gaffney, D. J., Elo, L. L., Zhang, X., & Mortazavi, A. (2016). A survey of best practices for RNA-seq data analysis. Genome Biol, 17, 13. https://doi.org/10.1186/s13059-016-0881-8

CORTES, C., & VAPNIK, V. (1995). . Machine Leaming 20(3). https://doi.org/https://doi.org/10.1023/A:1022627411411

de la Fuente, A. (2010). From 'differential expression' to 'differential networking' - identification of dysfunctional regulatory networks in diseases. Trends Genet, 26(7), 326-333. https://doi.org/10.1016/j.tig.2010.05.001

Diaz-Uriarte, R., & Alvarez de Andres, S. (2006). Gene selection and classification of microarray data using random forest. BMC Bioinformatics, 7, 3. https://doi.org/10.1186/1471-2105-7-3

Ding, X., Ma, Y., Li, S., Liu, J., Qin, L., & Wu, A. (2025). Influenza virus reassortment patterns exhibit preference and continuity while uncovering cross-species transmission events. Brief Bioinform, 26(3). https://doi.org/10.1093/bib/bbaf233

Eraslan, G., Avsec, Z., Gagneur, J., & Theis, F. J. (2019). Deep learning: new computational modelling techniques for genomics. Nat Rev Genet, 20(7), 389-403. https://doi.org/10.1038/s41576-019-0122-6

Evseev, D., & Magor, K. E. (2019). Innate Immune Responses to Avian Influenza Viruses in Ducks and Chickens. Vet Sci, 6(1). https://doi.org/10.3390/vetsci6010005

Fawcett, T. (2006). An introduction to ROC analysis. Pattern Recognition Letters, 27(8), 861-874. https://doi.org/10.1016/j.patrec.2005.10.010

Ge, S., Sun, S., Xu, H., Cheng, Q., & Ren, Z. (2025). Deep learning in single-cell and spatial transcriptomics data analysis: advances and challenges from a data science perspective. Brief Bioinform, 26(2). https://doi.org/10.1093/bib/bbaf136

Geoffrey S Ginsburg, S. B. H. (2006). . Expert Review of Molecular Diagnostics, 6(2). https://doi.org/https://doi.org/10.1586/14737159.6.2.179

Giotis, E. S., Robey, R. C., Skinner, N. G., Tomlinson, C. D., Goodbourn, S., & Skinner, M. A. (2016). Chicken interferome: avian interferon-stimulated genes identified by microarray and RNA-seq of primary chick embryo fibroblasts treated with a chicken type I interferon (IFN-alpha). Vet Res, 47(1), 75. https://doi.org/10.1186/s13567-016-0363-8

Golpasand, S., Ghovvati, S., & Pezeshkian, Z. (2025). Exploring the molecular and biological mechanisms of host response in chickens infected with highly pathogenic avian influenza virus (H5N1): An integrative transcriptomic analysis. PLoS One, 20(10), e0332689. https://doi.org/10.1371/journal.pone.0332689

Hassan, M. S. H., & Sharif, S. (2025). Immune responses to avian influenza viruses in chickens. Virology, 603, 110405. https://doi.org/10.1016/j.virol.2025.110405

He, X., Zhang, S., Zou, Z., Gao, P., Yang, L., & Xiang, B. (2024). Antiviral Effects of Avian Interferon-Stimulated Genes. Animals, 14(21). https://doi.org/10.3390/ani14213062

Huang, S., Chaudhary, K., & Garmire, L. X. (2017). More Is Better: Recent Progress in Multi-Omics Data Integration Methods. Front Genet, 8, 84. https://doi.org/10.3389/fgene.2017.00084

Hwang, H., Jeon, H., Yeo, N., & Baek, D. (2024). Big data and deep learning for RNA biology. Exp Mol Med, 56(6), 1293-1321. https://doi.org/10.1038/s12276-024-01243-w

Karczewski, K. J., & Snyder, M. P. (2018). Integrative omics for health and disease. Nat Rev Genet, 19(5), 299-310. https://doi.org/10.1038/nrg.2018.4

Krstajic, D., Buturovic, L. J., Leahy, D. E., & Thomas, S. (2014). Cross-validation pitfalls when selecting and assessing regression and classification models. J Cheminform, 6(1), 10. https://doi.org/10.1186/1758-2946-6-10

Kuchipudi, S. V., Dunham, S. P., & Chang, K. C. (2015). DNA microarray global gene expression analysis of influenza virus-infected chicken and duck cells. Genom Data, 4, 60-64. https://doi.org/10.1016/j.gdata.2015.03.004

Li, R., Li, L., Xu, Y., & Yang, J. . (2022). . Briefings in Bioinformatics 23(1). https://doi.org/10.1093/bib/bbab460

Libbrecht, M. W., & Noble, W. S. (2015). Machine learning applications in genetics and genomics. Nat Rev Genet, 16(6), 321-332. https://doi.org/10.1038/nrg3920

Liniger, M., Summerfield, A., Zimmer, G., McCullough, K. C., & Ruggli, N. (2012). Chicken Cells Sense Influenza A Virus Infection through MDA5 and CARDIF Signaling Involving LGP2. Journal of Virology, 86(2), 705-717. https://doi.org/10.1128/jvi.00742-11

Love, M. I., Huber, W., & Anders, S. (2014). Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2. Genome Biol, 15(12), 550. https://doi.org/10.1186/s13059-014-0550-8

Lowe, R., Shirley, N., Bleackley, M., Dolan, S., & Shafee, T. (2017). Transcriptomics technologies. PLoS Comput Biol, 13(5), e1005457. https://doi.org/10.1371/journal.pcbi.1005457

Mckinney, W. (2010). . Proceedings of the 9th Python in Science Conference. https://doi.org/https://doi.org/10.25080/Majora-92bf1922-00a

Morris, K. M., Mishra, A., Raut, A. A., Gaunt, E. R., Borowska, D., Kuo, R. I., Wang, B., Vijayakumar, P., Chingtham, S., Dutta, R., Baillie, K., Digard, P., Vervelde, L., Burt, D. W., & Smith, J. (2023). The molecular basis of differential host responses to avian influenza viruses in avian species with differing susceptibility. Front Cell Infect Microbiol, 13, 1067993. https://doi.org/10.3389/fcimb.2023.1067993

Noble, W. S. (2006). . NATURE BIOTECHNOLOGY, 24(12). https://doi.org/https://doi.org/10.1038/nbt1206-1565.

Overmyer, K. A., Shishkova, E., Miller, I. J., Balnis, J., Bernstein, M. N., Peters-Clarke, T. M., Meyer, J. G., Quan, Q., Muehlbauer, L. K., Trujillo, E. A., He, Y., Chopra, A., Chieng, H. C., Tiwari, A., Judson, M. A., Paulson, B., Brademan, D. R., Zhu, Y., Serrano, L. R., . . . Jaitovich, A. (2021). Large-Scale Multi-omic Analysis of COVID-19 Severity. Cell Syst, 12(1), 23-40 e27. https://doi.org/10.1016/j.cels.2020.10.003

Pedregosa, F., Varoquaux, G., Gramfort, A., Michel, V., Thirion, B., Grisel, O.,. (2011). . Journal of machine learning research, 12. https://doi.org/http://arxiv.org/abs/1201.0490

Perrone, L. A., Plowden, J. K., Garcia-Sastre, A., Katz, J. M., & Tumpey, T. M. (2008). H5N1 and 1918 pandemic influenza virus infection results in early and excessive infiltration of macrophages and neutrophils in the lungs of mice. PLoS Pathog, 4(8), e1000115. https://doi.org/10.1371/journal.ppat.1000115

Pichlmair, A., Lassnig, C., Eberle, C. A., Gorna, M. W., Baumann, C. L., Burkard, T. R., Burckstummer, T., Stefanovic, A., Krieger, S., Bennett, K. L., Rulicke, T., Weber, F., Colinge, J., Muller, M., & Superti-Furga, G. (2011). IFIT1 is an antiviral protein that recognizes 5'-triphosphate RNA. Nat Immunol, 12(7), 624-630. https://doi.org/10.1038/ni.2048

Raeven, R. H. M., van Riet, E., Meiring, H. D., Metz, B., & Kersten, G. F. A. (2019). Systems vaccinology and big data in the vaccine development chain. Immunology, 156(1), 33-46. https://doi.org/10.1111/imm.13012

Randhawa, G. S., Soltysiak, M. P. M., El Roz, H., de Souza, C. P. E., Hill, K. A., & Kari, L. (2020). Machine learning using intrinsic genomic signatures for rapid classification of novel pathogens: COVID-19 case study. Plos One, 15(4), e0232391. https://doi.org/10.1371/journal.pone.0232391

Reel, P. S., Reel, S., Pearson, E., Trucco, E., & Jefferson, E. (2021). Using machine learning approaches for multi-omics data analysis: A review. Biotechnol Adv, 49, 107739. https://doi.org/10.1016/j.biotechadv.2021.107739

Rehman, S., Effendi, M. H., Witaningruma, A. M., Nnabuikeb, U. E., Bilal, M., Abbas, A., Abbas, R. Z., & Hussain, K. (2022). Avian influenza (H5N1) virus, epidemiology and its effects on backyard poultry in Indonesia: a review. F1000Res, 11, 1321. https://doi.org/10.12688/f1000research.125878.2

Ringnér, M. (2008). . NATURE BIOTECHNOLOGY 26. https://doi.org/https://doi.org/10.1038/nbt0308-303

Robinson, M. D., McCarthy, D. J., & Smyth, G. K. (2010). edgeR: a Bioconductor package for differential expression analysis of digital gene expression data. Bioinformatics, 26(1), 139-140. https://doi.org/10.1093/bioinformatics/btp616

Sadler, A. J., & Williams, B. R. (2008). Interferon-inducible antiviral effectors. Nat Rev Immunol, 8(7), 559-568. https://doi.org/10.1038/nri2314

Shu, L., Zhao, Y., Kurt, Z., Byars, S. G., Tukiainen, T., Kettunen, J., Orozco, L. D., Pellegrini, M., Lusis, A. J., Ripatti, S., Zhang, B., Inouye, M., Makinen, V. P., & Yang, X. (2016). Mergeomics: multidimensional data integration to identify pathogenic perturbations to biological systems. BMC Genomics, 17(1), 874. https://doi.org/10.1186/s12864-016-3198-9

Smith, J., Smith, N., Yu, L., Paton, I. R., Gutowska, M. W., Forrest, H. L., Danner, A. F., Seiler, J. P., Digard, P., Webster, R. G., & Burt, D. W. (2015). A comparative analysis of host responses to avian influenza infection in ducks and chickens highlights a role for the interferon-induced transmembrane proteins in viral resistance. BMC Genomics, 16(1), 574. https://doi.org/10.1186/s12864-015-1778-8

Stark, R., Grzelak, M., & Hadfield, J. (2019). RNA sequencing: the teenage years. Nat Rev Genet, 20(11), 631-656. https://doi.org/10.1038/s41576-019-0150-2

Statnikov, A., Aliferis, C. F., Tsamardinos, I., Hardin, D., & Levy, S. (2005). A comprehensive evaluation of multicategory classification methods for microarray gene expression cancer diagnosis. Bioinformatics, 21(5), 631-643. https://doi.org/10.1093/bioinformatics/bti033

Swayne, D. E. (2012). Impact of vaccines and vaccination on global control of avian influenza. Avian Dis, 56(4 Suppl), 818-828. https://doi.org/10.1637/10183-041012-Review.1

Tarca, A. L., Carey, V. J., Chen, X. wen, Romero, R., & Drǎghici, S. . (2007). . PLoS computational biology 3(6). https://doi.org/10.1371/journal.pcbi.0030116

Toussaint, P. A., Leiser, F., Thiebes, S., Schlesner, M., Brors, B., & Sunyaev, A. (2023). Explainable artificial intelligence for omics data: a systematic mapping study. Brief Bioinform, 25(1). https://doi.org/10.1093/bib/bbad453

Vu, T. H., Hong, Y., Truong, A. D., Lee, S., Heo, J., Lillehoj, H. S., & Hong, Y. H. (2022). The highly pathogenic H5N1 avian influenza virus induces the mitogen-activated protein kinase signaling pathway in the trachea of two Ri chicken lines. Anim Biosci, 35(7), 964-974. https://doi.org/10.5713/ab.21.0420

Wang, Z., Gerstein, M., & Snyder, M. (2009). RNA-Seq: a revolutionary tool for transcriptomics. Nat Rev Genet, 10(1), 57-63. https://doi.org/10.1038/nrg2484

Westermann, A. J., Barquist, L., & Vogel, J. (2017). Resolving host-pathogen interactions by dual RNA-seq. PLoS Pathog, 13(2), e1006033. https://doi.org/10.1371/journal.ppat.1006033

Graphical Abstract

Downloads

Published

2026-06-22

Issue

Section

Articles

How to Cite

Keivan, F., & Nikbakht Brujeni, G. (2026). Machine learning-driven identification of immune signatures from RNA-Seq data in H5N1-infected chickens: a computational Immunology approach. Journal of Poultry Sciences and Avian Diseases. https://jpsad.com/index.php/jpsad/article/view/217

Similar Articles

21-30 of 70

You may also start an advanced similarity search for this article.

Most read articles by the same author(s)