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Stress significantly increases mortality following a secondary bacterial respiratory infection

A variety of mechanisms contribute to the viral-bacterial synergy which results in fatal secondary bacterial respiratory infections. Epidemiological investigations have implicated physical and psychological stressors as factors contributing to the incidence and severity of respiratory infections and...

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Autores principales: Hodgson, Paul D, Aich, Palok, Stookey, Joseph, Popowych, Yurij, Potter, Andrew, Babiuk, Lorne, Griebel, Philip J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3348069/
https://www.ncbi.nlm.nih.gov/pubmed/22435642
http://dx.doi.org/10.1186/1297-9716-43-21
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author Hodgson, Paul D
Aich, Palok
Stookey, Joseph
Popowych, Yurij
Potter, Andrew
Babiuk, Lorne
Griebel, Philip J
author_facet Hodgson, Paul D
Aich, Palok
Stookey, Joseph
Popowych, Yurij
Potter, Andrew
Babiuk, Lorne
Griebel, Philip J
author_sort Hodgson, Paul D
collection PubMed
description A variety of mechanisms contribute to the viral-bacterial synergy which results in fatal secondary bacterial respiratory infections. Epidemiological investigations have implicated physical and psychological stressors as factors contributing to the incidence and severity of respiratory infections and psychological stress alters host responses to experimental viral respiratory infections. The effect of stress on secondary bacterial respiratory infections has not, however, been investigated. A natural model of secondary bacterial respiratory infection in naive calves was used to determine if weaning and maternal separation (WMS) significantly altered mortality when compared to calves pre-adapted (PA) to this psychological stressor. Following weaning, calves were challenged with Mannheimia haemolytica four days after a primary bovine herpesvirus-1 (BHV-1) respiratory infection. Mortality doubled in WMS calves when compared to calves pre-adapted to weaning for two weeks prior to the viral respiratory infection. Similar results were observed in two independent experiments and fatal viral-bacterial synergy did not extend beyond the time of viral shedding. Virus shedding did not differ significantly between treatment groups but innate immune responses during viral infection, including IFN-γ secretion, the acute-phase inflammatory response, CD14 expression, and LPS-induced TNFα production, were significantly greater in WMS versus PA calves. These observations demonstrate that weaning and maternal separation at the time of a primary BHV-1 respiratory infection increased innate immune responses that correlated significantly with mortality following a secondary bacterial respiratory infection.
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spelling pubmed-33480692012-05-09 Stress significantly increases mortality following a secondary bacterial respiratory infection Hodgson, Paul D Aich, Palok Stookey, Joseph Popowych, Yurij Potter, Andrew Babiuk, Lorne Griebel, Philip J Vet Res Research A variety of mechanisms contribute to the viral-bacterial synergy which results in fatal secondary bacterial respiratory infections. Epidemiological investigations have implicated physical and psychological stressors as factors contributing to the incidence and severity of respiratory infections and psychological stress alters host responses to experimental viral respiratory infections. The effect of stress on secondary bacterial respiratory infections has not, however, been investigated. A natural model of secondary bacterial respiratory infection in naive calves was used to determine if weaning and maternal separation (WMS) significantly altered mortality when compared to calves pre-adapted (PA) to this psychological stressor. Following weaning, calves were challenged with Mannheimia haemolytica four days after a primary bovine herpesvirus-1 (BHV-1) respiratory infection. Mortality doubled in WMS calves when compared to calves pre-adapted to weaning for two weeks prior to the viral respiratory infection. Similar results were observed in two independent experiments and fatal viral-bacterial synergy did not extend beyond the time of viral shedding. Virus shedding did not differ significantly between treatment groups but innate immune responses during viral infection, including IFN-γ secretion, the acute-phase inflammatory response, CD14 expression, and LPS-induced TNFα production, were significantly greater in WMS versus PA calves. These observations demonstrate that weaning and maternal separation at the time of a primary BHV-1 respiratory infection increased innate immune responses that correlated significantly with mortality following a secondary bacterial respiratory infection. BioMed Central 2012 2012-03-21 /pmc/articles/PMC3348069/ /pubmed/22435642 http://dx.doi.org/10.1186/1297-9716-43-21 Text en Copyright ©2012 Hodgson et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Hodgson, Paul D
Aich, Palok
Stookey, Joseph
Popowych, Yurij
Potter, Andrew
Babiuk, Lorne
Griebel, Philip J
Stress significantly increases mortality following a secondary bacterial respiratory infection
title Stress significantly increases mortality following a secondary bacterial respiratory infection
title_full Stress significantly increases mortality following a secondary bacterial respiratory infection
title_fullStr Stress significantly increases mortality following a secondary bacterial respiratory infection
title_full_unstemmed Stress significantly increases mortality following a secondary bacterial respiratory infection
title_short Stress significantly increases mortality following a secondary bacterial respiratory infection
title_sort stress significantly increases mortality following a secondary bacterial respiratory infection
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3348069/
https://www.ncbi.nlm.nih.gov/pubmed/22435642
http://dx.doi.org/10.1186/1297-9716-43-21
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