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Record W4413380895 · doi:10.3389/fcimb.2025.1667802

Editorial: Interactions at the viral-host nexus in animals: from omics insights to immune modulation

2025· editorial· en· W4413380895 on OpenAlexaff
Shaolin Qu, Muhammad Munir, Jing Qian, Jia He, Jianzhong Wang, Xiaohong Xu

Bibliographic record

VenueFrontiers in Cellular and Infection Microbiology · 2025
Typeeditorial
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicMetabolomics and Mass Spectrometry Studies
Canadian institutionsUniversity of Alberta
Fundersnot available
KeywordsOmicsProteomicsGenomicsComputational biologyBiologyMetabolomicsSystems biologyDiseaseBiomarker discoveryProteomeBioinformaticsGenomeMedicineGeneticsGenePathology

Abstract

fetched live from OpenAlex

Multi-omics integration has emerged as a powerful approach for gaining insights into complex biological system. By combining data from genomics, transcriptomics, proteomics, metabolomics, or other omics layers. This strategy enables a richer understanding of hostpathogen interactions, disease mechanisms, and therapeutic targets. Current advancements include three key areas: applications of multi-omics integration, innovations in algorithmic approaches, and emerging fields where these techniques are being applied.Multi-omics integration enhances the ability to characterize and manage pathogens by providing comprehensive data-driven insights into disease pathogenesis, biomarker discovery, and therapeutic interventions. In terms of disease diagnosis, multi-omics dataspanning genomic, transcriptomic, proteomic, and metabolomic layers-has significantly improved early detection and cancer subtype classification (Milner and Lennerz, 2024) (Zhao et al., 2024). Pathogen genomics plays a crucial role in monitoring and forecasting outbreaks, integrating methods allows experts to track the spread of pathogens and identify emerging threats, thereby supporting evolutionary and epidemiological studies (Knijn et al., 2023;Wu et al., 2024). Multi-omics data also reveals potential mechanisms underlying disease pathogenesis. For example, joint analysis of multi-omics data in chronic liver disease (CLD) or psychiatric conditions linked to infectious pathogens highlights novel aspects for drug development (Lin et al., 2022;Okobi et al., 2024). Zheng et al. integrated virome data of bronchoalveolar lavage fluid (BALF) and peripheral blood samples to provide novel insights into pulmonary microbial ecology(Ning Zheng, 2025). Shaji et al. have combined the data of kinase-substrate phosphomotif pattern analysis on the SARS-CoV-2 proteome with literature review and in-silico protein-protein docking approach, presents a framework for predicting SARS-CoV-2 phosphosites, suggesting MAP2K1 to be a key host kinase (Shaji V, 2025). Therefore, multi-omics integration provides a multidimensional view of diseases, significantly improving diagnostics, surveillance, and treatment strategies in pathogen-related contexts.Algorithmic innovations are critical for overcoming challenges in multi-omics data analysis, such as handling high-dimensional datasets, integrating diverse omics layers, and improving predictive accuracy. Recent advances leverage deep learning, machine learning, and novel computational frameworks to enhance integration. Deep learning has revolutionized multiomics integration by enabling feature learning and flexible data fusion strategies. Methods like MoAGL-SA introduced adaptive integration techniques for cancer subtype classification, addressing key issues such as embedding sample structure information into the feature space (Cheng et al., 2024). Supervised deep generalized canonical correlation analysis (SDGCCA) is another innovation that models nonlinear correlations between omics manifolds, improving phenotype classification and revealing relevant biological mechanisms (Moon et al., 2022). These approaches categorize architectures-such as neural networks-that handle complex, non-linear relationships in multi-omics data, facilitating more robust predictions for disease subtypes and biomarker identification (Ballard et al., 2024;ElKarami et al., 2022). Innovations in single-cell multi-omics integration allow for joint analysis at the resolution of individual cells, providing insights into cellular heterogeneity and complex traits like therapeutic resistance and immune evasion. Techniques focus on integrating omics data at the singlecell level, making them accessible for non-experts and enhancing understanding of cell states and gene functions (Hu et al., 2024;Xiao et al., 2024). Additionally, machine learning-based natural language processing (NLP) algorithms are employed to automate the extraction of pathogen-specific information from literature, such as detecting papers on experimental pathogen studies. Tools such as READBiomed-Pathogens train models to identify and characterize mentions of pathogens in scientific texts, filling gaps in manually annotated corpora and accelerating knowledge discovery (Jimeno Yepes and Verspoor, 2023).These innovations address challenges like data dimensionality reduction, integration of sparse datasets, and the incorporation of machine learning for refinement, thereby enabling more intuitive and informative interpretations in pathogen research (Ngai et al., 2025).Driven by technological advancements, omics are expanding into novel aspects. For instance, the integration of multi-omics with electronic health records (EHR) and clinical imaging represents a frontier in precision health, allowing for disentangling host-microbe and hostenvironmental interactions (Babu and Snyder, 2023;Lin et al., 2022) . Wang et al. integrated proteomics and phosphoproteomics of freshwater mollusks to provide novel insights as potential food source(Tielin Wang, 2025). Additionally, Li et al. innovatively utilized humanized major histocompatibility complex (hMHC) murine models to reflect immune responses in SARS-CoV-2 infection, showing elevated immune response, especially IFN-γ signaling pathways and neutrophil mobilization dynamics that closely parallel human postvaccination responses, confirmed that the hMHC murine model can serve as an effective platform for vaccine research (Siyue Li, 2025). Chen et al. applied transcriptomic analysis to aquatilia, explained Chinese mitten crab immunity against bacterial infection, showing the differences between disease-resistant and susceptible species(Duanduan Chen, 2024). Research on novel or understudied pathogens emphasizes the need for multidisciplinary approaches, such as collaborations across animal, plant, and human disease contexts to understand cross-sectional involvement.Multi-omics integration has become a cornerstone of modern pathogen research, offering unprecedented capabilities in disease understanding, algorithmic processing, and crossdisciplinary applications. Through innovations in deep learning and machine learning-based algorithms, researchers can now better integrate complex datasets for improved disease prediction and pathogen-host interaction. Emerging fields, such as radiopathomics and spatial multi-omics, demonstrate the versatility of this approach, extending beyond human health into agriculture and environmental science. However, challenges still remain, including data integration hurdles and the need for high-quality annotations. Future directions emphasize collaborative efforts to refine multi-omics strategies and accelerate their implementation. Overall, these advancements highlight the transformative potential of multiomics integration in unlocking new frontiers in pathogen biology.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.005
metaresearch head score (Gemma)0.015
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Not applicable · Consensus signal: Not applicable
GenreCandidate signal: Editorial · Consensus signal: Editorial
Teacher disagreement score0.017
Threshold uncertainty score0.058

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0050.015
Meta-epidemiology (narrow)0.0030.001
Meta-epidemiology (broad)0.0030.003
Bibliometrics0.0030.001
Science and technology studies0.0020.002
Scholarly communication0.0050.004
Open science0.0030.001
Research integrity0.0130.015
Insufficient payload (model declined to judge)0.0170.012

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.004
GPT teacher head0.228
Teacher spread0.225 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designNot applicable
Domainnot available
GenreEditorial

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations1
Published2025
Admission routes1
Has abstractyes

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