Evidence map›Paper›PMID 41144480›Full record

ArticlePloS one2025

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

Nooshin Ghahramani, Ali Hashemi, Bahman Panahi

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Nooshin GhahramaniDepartment of Animal Science, Division of Animal Breeding and Genetics, Faculty of Agriculture, Urmia University, Urmia, Iran.
Ali HashemiDepartment of Animal Science, Division of Animal Breeding and Genetics, Faculty of Agriculture, Urmia University, Urmia, Iran.ORCID https://orcid.org/0009-0006-3740-2996
Bahman PanahiDepartment of Genomics, Northwest and West Branch, Agricultural Biotechnology Research Institute of Iran (ABRII), Agricultural Research, Education and Extension Organization (AREEO), Tabriz, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Bovine Respiratory Disease ComplexCattle DiseasesGene Regulatory NetworksAnimalsCattleGene Expression ProfilingGene Expression RegulationSignal TransductionSystems Biology

Identifiers

PMID41144480
PMCPMC12558457

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.