Potential Diagnostic Value of the Peripheral Blood Mononuclear Cell Transcriptome From Cattle With Bovine

Lichun Fang1, Weidong Lin1,2, Hong Jia1

  • 1Institute of Animal Sciences (IAS), Chinese Academy of Agricultural Sciences (CAAS), Beijing, China.

Insights

This study reveals immune responses in cattle with bovine tuberculosis (bTB) using RNA-Seq. Transcriptome analysis identified potential biomarkers for diagnosing bTB in infected cattle.

Area of Science:

  • Veterinary Immunology
  • Molecular Diagnostics
  • Transcriptomics

Background:

  • Bovine tuberculosis (bTB) is a significant chronic disease in cattle caused by Mycobacterium bovis.
  • Early-stage M. bovis infection involves shedding of mycobacteria, detectable via nested-polymerase chain reaction (PCR).
  • Limited research exists on immune responses in nested PCR-positive (bTB PCR-P) and nested PCR-negative (bTB PCR-N) M. bovis-infected cattle.

Purpose of the Study:

  • To investigate the transcriptomes of peripheral blood mononuclear cells (PBMCs) in bTB PCR-P, bTB PCR-N, and healthy cattle.
  • To explore the potential of PBMC transcripts as novel biomarkers for bTB diagnosis.
  • To compare immune responses between different cattle groups, with and without purified protein derivative of bovine tuberculin (PPD-B) stimulation.

Main Methods:

  • RNA-sequencing (RNA-Seq) was used to analyze PBMC transcriptomes.
  • Comparative analysis was performed between healthy, bTB PCR-P, and bTB PCR-N cattle groups.
  • Differential gene expression and pathway analysis were conducted, with and without PPD-B stimulation.

Main Results:

  • Numerous differentially expressed genes were identified across comparisons (adjusted p < 0.05).
  • Shared dysregulated pathways between bTB PCR-P and bTB PCR-N cattle included Cytokine-cytokine receptor interaction and NF-kappa B signaling.
  • Specific genes like Lymphotoxin alpha and Interleukin-8 showed potential for differentiating infected from healthy cattle, while B cell lymphoma 2 and Chitinase 3-like 1 differentiated between bTB PCR-P and bTB PCR-N.

Conclusions:

  • PBMC transcriptome analysis provides insights into immune responses in M. bovis-infected cattle.
  • Identified genes and pathways offer potential novel biomarkers for bTB diagnosis.
  • Further validation of identified biomarkers could enhance bTB diagnostic strategies.

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