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Immunobiology2015; 221(2); 236-244; doi: 10.1016/j.imbio.2015.09.002

Immune gene expression profiling of PBMC isolated from horses vaccinated with attenuated African horsesickness virus serotype 4.

Abstract: Development of African horsesickness (AHS) subunit vaccines will have to include a rational approach that uses knowledge of how the virus interacts with the host immune system. The global in vivo immune response induced by attenuated AHSV serotype 4 in horses was characterised using transcriptome sequencing. PBMC were collected with 24h intervals for four days after inoculation and four days after a second boost, 21 days later. Transcriptome data were normalised to the day 0 naïve transcriptome and up- or down-regulated immune genes identified using the CLC workbench. Peak expression was observed 24h after each inoculation. Innate immunity was up-regulated after both inoculations and was characterised by type-1 interferon activation via the RIG-1/MDA5 pathway and the up-regulation of complement cascade components. After the second boost an adaptive immune response could be identified that included the production of cytokines indicative of T helper (Th)1, Th2 and Th17 responses.
Publication Date: 2015-09-03 PubMed ID: 26382058DOI: 10.1016/j.imbio.2015.09.002Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This research article focuses on understanding the interaction between the African horsesickness (AHS) virus and a horse’s immune system in response to a vaccination. It particularly concentrates on observing any changes in the immune gene expression in the horse’s peripheral blood mononuclear cells (PBMC).

Understanding the Immune Response

The study aims to gather deeper insights into the global immune response generated in horses by the attenuated AHSV serotype 4 vaccine. It’s important to understand how a vaccine affects an animal’s immune response at a genetic level to develop more effective vaccines in future.

  • Peripheral blood mononuclear cells (PBMC) from vaccinated horses were collected at a frequency of every 24 hours for four days following the first vaccination, and again for four days after a second booster shot given 21 days later.
  • The gene expression profiles of these cells were then sequenced and analysed to identify immune genes that were either upregulated (increased in activity) or downregulated (decreased in activity).
  • These data were normalised to the gene expression profile of a naïve horse (day 0) who had not been exposed to the virus. This provided a baseline for comparison.

Observations and Findings

Analysis of the immune gene expression profiles revealed interesting dynamics in the immune response of the vaccinated horses.

  • The peak of gene expression was noted to occur 24 hours after each vaccination, indicative of an active immune response.
  • Following each inoculation, the innate immunity – the body’s first line of defence – was observed to be upregulated. This was characterized by the activation of type-1 interferon via the RIG-1/MDA5 pathway and an increased activity in the genes involved in the complement cascade, which is an important part of the immune response.
  • After the second booster shot, an enhanced adaptive immune response was noted. The adaptive immune response is a more specific, learned response informed by past exposure to pathogens. This response showed an increase in the production of cytokines connected to T helper (Th)1, Th2, and Th17 responses, which have distinct roles in immune regulation and disease course.

This study provides valuable insights into the mechanisms and timing of immune gene regulation in response to the AHSV serotype 4 vaccine, which may inform future vaccine research and development for African horsesickness.

Cite This Article

APA
Pretorius A, Faber FE, van Kleef M. (2015). Immune gene expression profiling of PBMC isolated from horses vaccinated with attenuated African horsesickness virus serotype 4. Immunobiology, 221(2), 236-244. https://doi.org/10.1016/j.imbio.2015.09.002

Publication

ISSN: 1878-3279
NlmUniqueID: 8002742
Country: Netherlands
Language: English
Volume: 221
Issue: 2
Pages: 236-244
PII: S0171-2985(15)30053-X

Researcher Affiliations

Pretorius, A
  • ARC-Onderstepoort Veterinary Institute, Private Bag X5, Onderstepoort 0110, South Africa. Electronic address: PretoriusAL@arc.agric.za.
Faber, F E
  • ARC-Onderstepoort Veterinary Institute, Private Bag X5, Onderstepoort 0110, South Africa.
van Kleef, M
  • ARC-Onderstepoort Veterinary Institute, Private Bag X5, Onderstepoort 0110, South Africa.

MeSH Terms

  • African Horse Sickness / genetics
  • African Horse Sickness / immunology
  • African Horse Sickness / prevention & control
  • African Horse Sickness / virology
  • African Horse Sickness Virus / drug effects
  • African Horse Sickness Virus / immunology
  • Animals
  • Antibodies, Viral / biosynthesis
  • Antibodies, Viral / blood
  • Complement System Proteins / genetics
  • Complement System Proteins / immunology
  • DEAD-box RNA Helicases / genetics
  • DEAD-box RNA Helicases / immunology
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Horses
  • Immunity, Active
  • Immunity, Innate / drug effects
  • Interferon Type I / genetics
  • Interferon Type I / immunology
  • Microarray Analysis
  • Serogroup
  • T-Lymphocytes, Helper-Inducer / drug effects
  • T-Lymphocytes, Helper-Inducer / immunology
  • T-Lymphocytes, Helper-Inducer / virology
  • Transcriptome / immunology
  • Vaccination
  • Vaccines, Attenuated
  • Viral Vaccines / administration & dosage

Citations

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