Whole-blood gene-expression profiles of cows infected with Mycobacterium avium subsp. paratuberculosis reveal changes in immune response and lipid metabolism

J Microbiol Biotechnol. 2015 Feb;25(2):255-67. doi: 10.4014/jmb.1408.08059.

Abstract

Mycobacterium avium subsp. paratuberculosis (MAP) is the causative agent of Johne's disease, a chronic debilitating disease affecting ruminants worldwide. In the present study, we aimed to determine the major gene networks and pathways underlying the immune response to MAP infection using whole-blood cells, as well as provide the potential transcriptional markers for identifying the status of MAP infection. We analyzed the transcriptional profiles of whole-blood cells of cattle identified and grouped according to the presence of MAP-specific antibodies and the MAP shed by them. The grouping was based on the results obtained by ELISA and PCR analyses as follows: i) Test1 group: MAP-negative results obtained by ELISA and positive results obtained by PCR; ii) Test2 group: MAP-positive results obtained by ELISA and negative results obtained by PCR; iii) Test3 group: MAP-positive results obtained by ELISA and positive results obtained by PCR; iv) uninfected control: MAP-negative results obtained both by ELISA and PCR analysis. The results showed down-regulated production and metabolism of reactive oxygen species in the Test1 group, activation of pathways related to the host-defense response against MAP (LXR/RXR activation and complement system) in the Test2 and Test3 groups, and anti-inflammatory response (activation of IL-10 signaling pathway) only in the Test3 group. Our data indicate a balanced response that serves the immune-limiting mechanism while the host-defense responses are progressing.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Bacterial / blood
  • Blood Cells / immunology*
  • Blood Cells / metabolism*
  • Cattle
  • Cattle Diseases / genetics*
  • Cattle Diseases / immunology
  • Cattle Diseases / metabolism
  • Complement System Proteins / genetics
  • Down-Regulation
  • Enzyme-Linked Immunosorbent Assay
  • Gene Expression Profiling*
  • Gene Regulatory Networks
  • Immunity, Cellular
  • Lipid Metabolism*
  • Microarray Analysis
  • Mycobacterium avium subsp. paratuberculosis / immunology*
  • Paratuberculosis / genetics*
  • Paratuberculosis / immunology
  • Paratuberculosis / metabolism
  • Reactive Oxygen Species / metabolism
  • Real-Time Polymerase Chain Reaction
  • Signal Transduction
  • Up-Regulation

Substances

  • Antibodies, Bacterial
  • Reactive Oxygen Species
  • Complement System Proteins