# Weighted gene co-expression network analysis identifies functional modules related to bovine respiratory disease

## TL;DR

This study uses gene network analysis to identify immune-related gene modules and key regulators linked to bovine respiratory disease in cattle.

## Contribution

The study introduces an integrative approach combining meta-analysis, co-expression networks, and machine learning to uncover novel gene modules and biomarkers for BRD.

## Key findings

- Six functional gene modules were identified, with altered connectivity in BRD-affected cattle.
- CFB gene expression was found to correlate with BRD susceptibility and clinical symptoms.
- Key transcription factors like GABPA and TCF4 were linked to immune pathways in BRD.

## Abstract

Bovine respiratory disease (BRD) is a multifactorial disease of dairy and beef cattle that involves complex interactions with the host immune system. In the current study, a comprehensive meta-analysis was performed using a P-value combination approach. In the next step, the identified meta-genes were subjected to systems biology analysis using the weighted gene co-expression network analysis (WGCNA) method. Subsequently, the most functionally important modules and genes were validated using machine learning algorithms. Finally, the critical regulatory network associated with BRD was constructed. A total of 1,908 common meta-genes were identified through the combined analysis of differentially expressed genes (DEGs) using the Fisher and Invorm approaches. Co-expression network analysis confirmed six functional modules, among which the connectivity patterns of the blue, brown, green, and yellow modules were significantly altered in BRD-affected cattle compared with healthy controls. Functional enrichment analysis of the significant modules revealed that the ‘Salmonella infection,’ ‘NOD-like receptor signaling pathway,’ ‘Necroptosis,’ ‘Toll-like receptor signaling pathway,’ ‘TNF signaling pathway,’ ‘IL-17 signaling pathway,’ ‘Apoptosis,’ and ‘Influenza A’ pathways were the most significantly associated with BRD. The constructed regulatory network identified GABPA, TCF4, ELK1, NR2C2, and ARNT as key transcription factors (TFs), each playing a central role in regulating immune and inflammatory pathways implicated in BRD. Finally, the constructed model revealed that differential expression of the CFB gene is significantly associated with susceptibility to BRD. In cattle, CFB expression correlates with clinical signs of respiratory disease, supporting its potential as a biomarker. Moreover, the involvement of CFB in modulating pro-inflammatory cytokines (e.g., TNF) and its integration with other immune-related pathways (e.g., NF-κB signaling) further highlight its relevance as a biomarker. Overall, this integrative approach enhances our understanding of the molecular mechanisms underlying BRD and provides a foundation for developing diagnostic, therapeutic, and genetic selection strategies to improve cattle health and disease resistance.