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

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 exp...

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Autores principales: Hjertner, Bernt, Lützelschwab, Claudia, Schieck, Elise, Nzau, Benjamin, Henson, Sonal, Sjölund, Marie, Fossum, Caroline, Magnusson, Ulf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8459988/
https://www.ncbi.nlm.nih.gov/pubmed/34555028
http://dx.doi.org/10.1371/journal.pone.0256106
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author Hjertner, Bernt
Lützelschwab, Claudia
Schieck, Elise
Nzau, Benjamin
Henson, Sonal
Sjölund, Marie
Fossum, Caroline
Magnusson, Ulf
author_facet Hjertner, Bernt
Lützelschwab, Claudia
Schieck, Elise
Nzau, Benjamin
Henson, Sonal
Sjölund, Marie
Fossum, Caroline
Magnusson, Ulf
author_sort Hjertner, Bernt
collection PubMed
description 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.
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spelling pubmed-84599882021-09-24 Development of a 3-transcript host expression assay to differentiate between viral and bacterial infections in pigs Hjertner, Bernt Lützelschwab, Claudia Schieck, Elise Nzau, Benjamin Henson, Sonal Sjölund, Marie Fossum, Caroline Magnusson, Ulf PLoS One Research Article 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. Public Library of Science 2021-09-23 /pmc/articles/PMC8459988/ /pubmed/34555028 http://dx.doi.org/10.1371/journal.pone.0256106 Text en © 2021 Hjertner et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Hjertner, Bernt
Lützelschwab, Claudia
Schieck, Elise
Nzau, Benjamin
Henson, Sonal
Sjölund, Marie
Fossum, Caroline
Magnusson, Ulf
Development of a 3-transcript host expression assay to differentiate between viral and bacterial infections in pigs
title Development of a 3-transcript host expression assay to differentiate between viral and bacterial infections in pigs
title_full Development of a 3-transcript host expression assay to differentiate between viral and bacterial infections in pigs
title_fullStr Development of a 3-transcript host expression assay to differentiate between viral and bacterial infections in pigs
title_full_unstemmed Development of a 3-transcript host expression assay to differentiate between viral and bacterial infections in pigs
title_short Development of a 3-transcript host expression assay to differentiate between viral and bacterial infections in pigs
title_sort development of a 3-transcript host expression assay to differentiate between viral and bacterial infections in pigs
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8459988/
https://www.ncbi.nlm.nih.gov/pubmed/34555028
http://dx.doi.org/10.1371/journal.pone.0256106
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