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The acute phase response of haptoglobin and serum amyloid A (SAA) in cattle undergoing experimental infection with bovine respiratory syncytial virus
The ability of a pure virus infection to induce an acute phase protein response is of interest as viral infections are normally considered to be less efficient in inducing an acute phase protein response than bacterial infections. This was studied in a bovine model for infection with bovine respirat...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science B.V.
2000
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7119828/ https://www.ncbi.nlm.nih.gov/pubmed/11068073 http://dx.doi.org/10.1016/S0165-2427(00)00226-9 |
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author | Heegaard, Peter M.H Godson, Dale L Toussaint, Mathilda J.M Tjørnehøj, Kirsten Larsen, Lars E Viuff, Birgitte Rønsholt, Leif |
author_facet | Heegaard, Peter M.H Godson, Dale L Toussaint, Mathilda J.M Tjørnehøj, Kirsten Larsen, Lars E Viuff, Birgitte Rønsholt, Leif |
author_sort | Heegaard, Peter M.H |
collection | PubMed |
description | The ability of a pure virus infection to induce an acute phase protein response is of interest as viral infections are normally considered to be less efficient in inducing an acute phase protein response than bacterial infections. This was studied in a bovine model for infection with bovine respiratory syncytial virus (BRSV), analysing the induction of the two most dominant bovine acute phase proteins haptoglobin and serum amyloid A (SAA). Strong and reproducible acute phase responses were detected for both proteins, peaking at around 7–8 days after inoculation of BRSV, while no response was seen in mock-inoculated control animals. The serum concentrations reached for SAA and haptoglobin during the BRSV-induced acute phase response were generally the same or higher than previously reported for bacterial infections in calves. The magnitude and the duration of the haptoglobin response was found to correlate well with the severity of clinical signs (fever) and with the extent of lung consolidation while SAA responded most rapidly to infection. |
format | Online Article Text |
id | pubmed-7119828 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | Elsevier Science B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71198282020-04-08 The acute phase response of haptoglobin and serum amyloid A (SAA) in cattle undergoing experimental infection with bovine respiratory syncytial virus Heegaard, Peter M.H Godson, Dale L Toussaint, Mathilda J.M Tjørnehøj, Kirsten Larsen, Lars E Viuff, Birgitte Rønsholt, Leif Vet Immunol Immunopathol Article The ability of a pure virus infection to induce an acute phase protein response is of interest as viral infections are normally considered to be less efficient in inducing an acute phase protein response than bacterial infections. This was studied in a bovine model for infection with bovine respiratory syncytial virus (BRSV), analysing the induction of the two most dominant bovine acute phase proteins haptoglobin and serum amyloid A (SAA). Strong and reproducible acute phase responses were detected for both proteins, peaking at around 7–8 days after inoculation of BRSV, while no response was seen in mock-inoculated control animals. The serum concentrations reached for SAA and haptoglobin during the BRSV-induced acute phase response were generally the same or higher than previously reported for bacterial infections in calves. The magnitude and the duration of the haptoglobin response was found to correlate well with the severity of clinical signs (fever) and with the extent of lung consolidation while SAA responded most rapidly to infection. Elsevier Science B.V. 2000-11-23 2000-11-02 /pmc/articles/PMC7119828/ /pubmed/11068073 http://dx.doi.org/10.1016/S0165-2427(00)00226-9 Text en Copyright © 2000 Elsevier Science B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Heegaard, Peter M.H Godson, Dale L Toussaint, Mathilda J.M Tjørnehøj, Kirsten Larsen, Lars E Viuff, Birgitte Rønsholt, Leif The acute phase response of haptoglobin and serum amyloid A (SAA) in cattle undergoing experimental infection with bovine respiratory syncytial virus |
title | The acute phase response of haptoglobin and serum amyloid A (SAA) in cattle undergoing experimental infection with bovine respiratory syncytial virus |
title_full | The acute phase response of haptoglobin and serum amyloid A (SAA) in cattle undergoing experimental infection with bovine respiratory syncytial virus |
title_fullStr | The acute phase response of haptoglobin and serum amyloid A (SAA) in cattle undergoing experimental infection with bovine respiratory syncytial virus |
title_full_unstemmed | The acute phase response of haptoglobin and serum amyloid A (SAA) in cattle undergoing experimental infection with bovine respiratory syncytial virus |
title_short | The acute phase response of haptoglobin and serum amyloid A (SAA) in cattle undergoing experimental infection with bovine respiratory syncytial virus |
title_sort | acute phase response of haptoglobin and serum amyloid a (saa) in cattle undergoing experimental infection with bovine respiratory syncytial virus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7119828/ https://www.ncbi.nlm.nih.gov/pubmed/11068073 http://dx.doi.org/10.1016/S0165-2427(00)00226-9 |
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