Development of a 3-transcript host expression assay to differentiate between viral and bacterial infections in pigs

PLoS One. 2021 Sep 23;16(9):e0256106. doi: 10.1371/journal.pone.0256106. eCollection 2021.

Abstract

Indiscriminate use of antibiotics to treat infections that are of viral origin contributes to unnecessary use which potentially may induce resistance in commensal bacteria. To counteract this a number of host gene transcriptional studies have been conducted to identify genes that are differently expressed during bacterial and viral infections in humans, and thus could be used as a tool to base decisions on the use of antibiotics. In this paper, we aimed to evaluate the potential of a selection of genes that have been considered biomarkers in humans, to differentially diagnose bacterial from viral infections in the pig. First porcine PBMC were induced with six toll-like receptor (TLR) agonists (FliC, LPS, ODN 2216, Pam3CSK4, poly I:C, R848) to mimic host gene expression induced by bacterial or viral pathogens, or exposed to heat-killed Actinobacillus pleuropneumoniae or a split influenza virus. Genes that were differentially expressed between bacterial and viral inducers were further evaluated on clinical material comprising eleven healthy pigs, and six pigs infected with A. pleuropneumoniae. This comprised three virally upregulated genes (IFI44L, MxA, RSAD2) and four bacterially upregulated genes (IL-1β, IL-8, FAM89A, S100PBP). All six infected pigs could be differentially diagnosed to healthy pigs using a host gene transcription assay based on the geometric average of the bacterially induced genes IL-8 and S100PBP over that of the virally induced gene MxA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacteria / classification*
  • Bacteria / isolation & purification
  • Bacterial Infections / diagnosis*
  • Bacterial Infections / genetics
  • Bacterial Infections / microbiology
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Biological Assay
  • Leukocytes, Mononuclear / microbiology
  • Leukocytes, Mononuclear / pathology
  • Leukocytes, Mononuclear / virology
  • Swine
  • Swine Diseases / diagnosis*
  • Swine Diseases / genetics
  • Swine Diseases / microbiology
  • Swine Diseases / virology
  • Viral Proteins / genetics
  • Viral Proteins / metabolism*
  • Virus Diseases / diagnosis*
  • Virus Diseases / genetics
  • Virus Diseases / virology
  • Viruses / classification*
  • Viruses / isolation & purification

Substances

  • Bacterial Proteins
  • Viral Proteins

Grants and funding

This study was financially supported by the Animal Health Flagship of the CGIAR research Program on Livestock (https://livestock.cgiar.org). Department of Biomedical Sciences and Veterinary Public Health (Uppsala, Sweden) and the International Livestock Research Institute (Nairobi, Kenya) were allocated funds by the Animal Health Flagship to perform this study (consumables and salaries). BH, CL, ES and UM received parts of their salaries from this fund. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.