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Resistance to coronavirus infection in amino peptidase N-deficient pigs

The alphacoronaviruses, transmissible gastroenteritis virus (TGEV) and Porcine epidemic diarrhea virus (PEDV) are sources of high morbidity and mortality in neonatal pigs, a consequence of dehydration caused by the infection and necrosis of enterocytes. The biological relevance of amino peptidase N...

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Autores principales: Whitworth, Kristin M., Rowland, Raymond R. R., Petrovan, Vlad, Sheahan, Maureen, Cino-Ozuna, Ada G., Fang, Ying, Hesse, Richard, Mileham, Alan, Samuel, Melissa S., Wells, Kevin D., Prather, Randall S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6353812/
https://www.ncbi.nlm.nih.gov/pubmed/30315482
http://dx.doi.org/10.1007/s11248-018-0100-3
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author Whitworth, Kristin M.
Rowland, Raymond R. R.
Petrovan, Vlad
Sheahan, Maureen
Cino-Ozuna, Ada G.
Fang, Ying
Hesse, Richard
Mileham, Alan
Samuel, Melissa S.
Wells, Kevin D.
Prather, Randall S.
author_facet Whitworth, Kristin M.
Rowland, Raymond R. R.
Petrovan, Vlad
Sheahan, Maureen
Cino-Ozuna, Ada G.
Fang, Ying
Hesse, Richard
Mileham, Alan
Samuel, Melissa S.
Wells, Kevin D.
Prather, Randall S.
author_sort Whitworth, Kristin M.
collection PubMed
description The alphacoronaviruses, transmissible gastroenteritis virus (TGEV) and Porcine epidemic diarrhea virus (PEDV) are sources of high morbidity and mortality in neonatal pigs, a consequence of dehydration caused by the infection and necrosis of enterocytes. The biological relevance of amino peptidase N (ANPEP) as a putative receptor for TGEV and PEDV in pigs was evaluated by using CRISPR/Cas9 to edit exon 2 of ANPEP resulting in a premature stop codon. Knockout pigs possessing the null ANPEP phenotype and age matched wild type pigs were challenged with either PEDV or TGEV. Fecal swabs were collected daily from each animal beginning 1 day prior to challenge with PEDV until the termination of the study. The presence of virus nucleic acid was determined by PCR. ANPEP null pigs did not support infection with TGEV, but retained susceptibility to infection with PEDV. Immunohistochemistry confirmed the presence of PEDV reactivity and absence of TGEV reactivity in the enterocytes lining the ileum in ANPEP null pigs. The different receptor requirements for TGEV and PEDV have important implications in the development of new genetic tools for the control of enteric disease in pigs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11248-018-0100-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-63538122019-02-21 Resistance to coronavirus infection in amino peptidase N-deficient pigs Whitworth, Kristin M. Rowland, Raymond R. R. Petrovan, Vlad Sheahan, Maureen Cino-Ozuna, Ada G. Fang, Ying Hesse, Richard Mileham, Alan Samuel, Melissa S. Wells, Kevin D. Prather, Randall S. Transgenic Res Original Paper The alphacoronaviruses, transmissible gastroenteritis virus (TGEV) and Porcine epidemic diarrhea virus (PEDV) are sources of high morbidity and mortality in neonatal pigs, a consequence of dehydration caused by the infection and necrosis of enterocytes. The biological relevance of amino peptidase N (ANPEP) as a putative receptor for TGEV and PEDV in pigs was evaluated by using CRISPR/Cas9 to edit exon 2 of ANPEP resulting in a premature stop codon. Knockout pigs possessing the null ANPEP phenotype and age matched wild type pigs were challenged with either PEDV or TGEV. Fecal swabs were collected daily from each animal beginning 1 day prior to challenge with PEDV until the termination of the study. The presence of virus nucleic acid was determined by PCR. ANPEP null pigs did not support infection with TGEV, but retained susceptibility to infection with PEDV. Immunohistochemistry confirmed the presence of PEDV reactivity and absence of TGEV reactivity in the enterocytes lining the ileum in ANPEP null pigs. The different receptor requirements for TGEV and PEDV have important implications in the development of new genetic tools for the control of enteric disease in pigs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11248-018-0100-3) contains supplementary material, which is available to authorized users. Springer International Publishing 2018-10-12 2019 /pmc/articles/PMC6353812/ /pubmed/30315482 http://dx.doi.org/10.1007/s11248-018-0100-3 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Paper
Whitworth, Kristin M.
Rowland, Raymond R. R.
Petrovan, Vlad
Sheahan, Maureen
Cino-Ozuna, Ada G.
Fang, Ying
Hesse, Richard
Mileham, Alan
Samuel, Melissa S.
Wells, Kevin D.
Prather, Randall S.
Resistance to coronavirus infection in amino peptidase N-deficient pigs
title Resistance to coronavirus infection in amino peptidase N-deficient pigs
title_full Resistance to coronavirus infection in amino peptidase N-deficient pigs
title_fullStr Resistance to coronavirus infection in amino peptidase N-deficient pigs
title_full_unstemmed Resistance to coronavirus infection in amino peptidase N-deficient pigs
title_short Resistance to coronavirus infection in amino peptidase N-deficient pigs
title_sort resistance to coronavirus infection in amino peptidase n-deficient pigs
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6353812/
https://www.ncbi.nlm.nih.gov/pubmed/30315482
http://dx.doi.org/10.1007/s11248-018-0100-3
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