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Mucosal Immune Response to Feline Enteric Coronavirus Infection
Feline infectious peritonitis is a devastating, fatal disease of domestic cats caused by a pathogenic mutant virus derived from the ubiquitous feline enteric coronavirus (FECV). Infection by FECV is generally subclinical, and little is known about the mucosal immune response that controls and elimin...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6832150/ https://www.ncbi.nlm.nih.gov/pubmed/31569783 http://dx.doi.org/10.3390/v11100906 |
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author | Pearson, Morgan LaVoy, Alora Evans, Samantha Vilander, Allison Webb, Craig Graham, Barbara Musselman, Esther LeCureux, Jonathan VandeWoude, Sue Dean, Gregg A. |
author_facet | Pearson, Morgan LaVoy, Alora Evans, Samantha Vilander, Allison Webb, Craig Graham, Barbara Musselman, Esther LeCureux, Jonathan VandeWoude, Sue Dean, Gregg A. |
author_sort | Pearson, Morgan |
collection | PubMed |
description | Feline infectious peritonitis is a devastating, fatal disease of domestic cats caused by a pathogenic mutant virus derived from the ubiquitous feline enteric coronavirus (FECV). Infection by FECV is generally subclinical, and little is known about the mucosal immune response that controls and eliminates the virus. We investigated the mucosal immune response against FECV in an endemically infected breeding colony over a seven-month period. Thirty-three cats were grouped according to FECV seropositivity and fecal virus shedding into naïve/immunologically quiescent, convalescent and actively infected groups. Blood, fecal samples and colon biopsies were collected to assess the mucosal and systemic immunologic and virologic profile. Results showed that cats with active FECV infections have strong systemic IgG and mucosal IgA responses that wane after virus clearance. Significant FECV-specific mucosal T cell IFNγ responses were not detected in any of the three groups. A shift toward an inflammatory state in the mucosa was suggested by increased IL17:FoxP3 expression. However, no histologic abnormalities were observed, and no shifts in lymphocyte subpopulation phenotype or proliferation were noted. Together, the results suggest that control of FECV is mediated by humoral mucosal and systemic responses and that perturbations in the primary reservoir organ (colon) are minimal. |
format | Online Article Text |
id | pubmed-6832150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-68321502019-11-20 Mucosal Immune Response to Feline Enteric Coronavirus Infection Pearson, Morgan LaVoy, Alora Evans, Samantha Vilander, Allison Webb, Craig Graham, Barbara Musselman, Esther LeCureux, Jonathan VandeWoude, Sue Dean, Gregg A. Viruses Article Feline infectious peritonitis is a devastating, fatal disease of domestic cats caused by a pathogenic mutant virus derived from the ubiquitous feline enteric coronavirus (FECV). Infection by FECV is generally subclinical, and little is known about the mucosal immune response that controls and eliminates the virus. We investigated the mucosal immune response against FECV in an endemically infected breeding colony over a seven-month period. Thirty-three cats were grouped according to FECV seropositivity and fecal virus shedding into naïve/immunologically quiescent, convalescent and actively infected groups. Blood, fecal samples and colon biopsies were collected to assess the mucosal and systemic immunologic and virologic profile. Results showed that cats with active FECV infections have strong systemic IgG and mucosal IgA responses that wane after virus clearance. Significant FECV-specific mucosal T cell IFNγ responses were not detected in any of the three groups. A shift toward an inflammatory state in the mucosa was suggested by increased IL17:FoxP3 expression. However, no histologic abnormalities were observed, and no shifts in lymphocyte subpopulation phenotype or proliferation were noted. Together, the results suggest that control of FECV is mediated by humoral mucosal and systemic responses and that perturbations in the primary reservoir organ (colon) are minimal. MDPI 2019-09-27 /pmc/articles/PMC6832150/ /pubmed/31569783 http://dx.doi.org/10.3390/v11100906 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Pearson, Morgan LaVoy, Alora Evans, Samantha Vilander, Allison Webb, Craig Graham, Barbara Musselman, Esther LeCureux, Jonathan VandeWoude, Sue Dean, Gregg A. Mucosal Immune Response to Feline Enteric Coronavirus Infection |
title | Mucosal Immune Response to Feline Enteric Coronavirus Infection |
title_full | Mucosal Immune Response to Feline Enteric Coronavirus Infection |
title_fullStr | Mucosal Immune Response to Feline Enteric Coronavirus Infection |
title_full_unstemmed | Mucosal Immune Response to Feline Enteric Coronavirus Infection |
title_short | Mucosal Immune Response to Feline Enteric Coronavirus Infection |
title_sort | mucosal immune response to feline enteric coronavirus infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6832150/ https://www.ncbi.nlm.nih.gov/pubmed/31569783 http://dx.doi.org/10.3390/v11100906 |
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