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Systemic influenza virus H5N1 infection in cats after gastrointestinal exposure

Please cite this paper as: Vahlenkamp et al. (2010) Systemic influenza virus H5N1 infection in cats after gastrointestinal exposure. Influenza and Other Respiratory Viruses 4(6), 379–386. Background  Highly pathogenic avian influenza virus (HPAIV) H5N1 infections in felids have been reported in seve...

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Autores principales: Vahlenkamp, Thomas W., Teifke, Jens P., Harder, Timm C., Beer, Martin, Mettenleiter, Thomas C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4634607/
https://www.ncbi.nlm.nih.gov/pubmed/20958932
http://dx.doi.org/10.1111/j.1750-2659.2010.00173.x
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author Vahlenkamp, Thomas W.
Teifke, Jens P.
Harder, Timm C.
Beer, Martin
Mettenleiter, Thomas C.
author_facet Vahlenkamp, Thomas W.
Teifke, Jens P.
Harder, Timm C.
Beer, Martin
Mettenleiter, Thomas C.
author_sort Vahlenkamp, Thomas W.
collection PubMed
description Please cite this paper as: Vahlenkamp et al. (2010) Systemic influenza virus H5N1 infection in cats after gastrointestinal exposure. Influenza and Other Respiratory Viruses 4(6), 379–386. Background  Highly pathogenic avian influenza virus (HPAIV) H5N1 infections in felids have been reported in several countries. Feeding on infected birds has been suggested as potential source of infection. Objectives  The study aimed to verify gastrointestinal infection as possible portal of entry for HPAIV H5N1 in cats. Methods  Four cats were infected oculo‐nasopharyngeally with 10(6) 50% egg infectious dose (EID(50)) of HPAIV H5N1 A/cat/Germany/R606/2006. Two cats were infected intravenously with 10(6) EID(50) and two cats were inoculated orally with 10(7) EID(50) HPAIV embedded in gelatine capsules to mimic gastrointestinal exposure and to avoid virus contact to oropharyngeal or respiratory tissues. Cats were monitored for 6 days by physical examination, virus excretion, and peripheral blood lymphocyte counts. Blood chemical parameters (including AST, ALT, CPK, and TBIL) and viral excretion using pharyngeal and rectal swabs were analyzed. Results  Infected cats showed elevated body temperature up to 41·3°C starting from day 1 or 2 p.i. All infected cats excreted virus in pharyngeal swabs within 2 days p.i. co‐inciding with the development of clinical signs (anorexia, depression, and labored breathing) irrespective of the infection route. Virus dissemination occurred through cell‐free and cell‐associated viremia. Infected cats developed lymphopenia, hepatic necrosis, pneumonia, and significantly elevated levels of aspartate aminotransferase (AST), alanine aminotransferase (ALT), creatine phosphokinase (CPK), and TBIL. Conclusions  The experiments show that the gastrointestinal tract can serve as portal for the entry of HPAIV H5N1 into cats. Infection routes used did not influence viral tissue tropism and course of disease.
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spelling pubmed-46346072015-11-30 Systemic influenza virus H5N1 infection in cats after gastrointestinal exposure Vahlenkamp, Thomas W. Teifke, Jens P. Harder, Timm C. Beer, Martin Mettenleiter, Thomas C. Influenza Other Respir Viruses Original Articles Please cite this paper as: Vahlenkamp et al. (2010) Systemic influenza virus H5N1 infection in cats after gastrointestinal exposure. Influenza and Other Respiratory Viruses 4(6), 379–386. Background  Highly pathogenic avian influenza virus (HPAIV) H5N1 infections in felids have been reported in several countries. Feeding on infected birds has been suggested as potential source of infection. Objectives  The study aimed to verify gastrointestinal infection as possible portal of entry for HPAIV H5N1 in cats. Methods  Four cats were infected oculo‐nasopharyngeally with 10(6) 50% egg infectious dose (EID(50)) of HPAIV H5N1 A/cat/Germany/R606/2006. Two cats were infected intravenously with 10(6) EID(50) and two cats were inoculated orally with 10(7) EID(50) HPAIV embedded in gelatine capsules to mimic gastrointestinal exposure and to avoid virus contact to oropharyngeal or respiratory tissues. Cats were monitored for 6 days by physical examination, virus excretion, and peripheral blood lymphocyte counts. Blood chemical parameters (including AST, ALT, CPK, and TBIL) and viral excretion using pharyngeal and rectal swabs were analyzed. Results  Infected cats showed elevated body temperature up to 41·3°C starting from day 1 or 2 p.i. All infected cats excreted virus in pharyngeal swabs within 2 days p.i. co‐inciding with the development of clinical signs (anorexia, depression, and labored breathing) irrespective of the infection route. Virus dissemination occurred through cell‐free and cell‐associated viremia. Infected cats developed lymphopenia, hepatic necrosis, pneumonia, and significantly elevated levels of aspartate aminotransferase (AST), alanine aminotransferase (ALT), creatine phosphokinase (CPK), and TBIL. Conclusions  The experiments show that the gastrointestinal tract can serve as portal for the entry of HPAIV H5N1 into cats. Infection routes used did not influence viral tissue tropism and course of disease. Blackwell Publishing Ltd 2010-08-24 2010-11 /pmc/articles/PMC4634607/ /pubmed/20958932 http://dx.doi.org/10.1111/j.1750-2659.2010.00173.x Text en © 2010 Blackwell Publishing Ltd
spellingShingle Original Articles
Vahlenkamp, Thomas W.
Teifke, Jens P.
Harder, Timm C.
Beer, Martin
Mettenleiter, Thomas C.
Systemic influenza virus H5N1 infection in cats after gastrointestinal exposure
title Systemic influenza virus H5N1 infection in cats after gastrointestinal exposure
title_full Systemic influenza virus H5N1 infection in cats after gastrointestinal exposure
title_fullStr Systemic influenza virus H5N1 infection in cats after gastrointestinal exposure
title_full_unstemmed Systemic influenza virus H5N1 infection in cats after gastrointestinal exposure
title_short Systemic influenza virus H5N1 infection in cats after gastrointestinal exposure
title_sort systemic influenza virus h5n1 infection in cats after gastrointestinal exposure
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4634607/
https://www.ncbi.nlm.nih.gov/pubmed/20958932
http://dx.doi.org/10.1111/j.1750-2659.2010.00173.x
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