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Disruption of anthrax toxin receptor 1 in pigs leads to a rare disease phenotype and protection from senecavirus A infection

Senecavirus A (SVA) is a cause of vesicular disease in pigs, and infection rates are rising within the swine industry. Recently, anthrax toxin receptor 1 (ANTXR1) was revealed as the receptor for SVA in human cells. Herein, the role of ANTXR1 as a receptor for SVA in pigs was investigated by CRISPR/...

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Autores principales: Chen, Paula R., Rowland, Raymond R. R., Stoian, Ana M., Petrovan, Vlad, Sheahan, Maureen, Ganta, Charan, Cino-Ozuna, Giselle, Kim, Dae Young, Dunleavey, James M., Whitworth, Kristin M., Samuel, Melissa S., Spate, Lee D., Cecil, Raissa F., Benne, Joshua A., Yan, Xingyu, Fang, Ying, Croix, Brad St., Lechtenberg, Kelly, Wells, Kevin D., Prather, Randall S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8943192/
https://www.ncbi.nlm.nih.gov/pubmed/35322150
http://dx.doi.org/10.1038/s41598-022-09123-x
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author Chen, Paula R.
Rowland, Raymond R. R.
Stoian, Ana M.
Petrovan, Vlad
Sheahan, Maureen
Ganta, Charan
Cino-Ozuna, Giselle
Kim, Dae Young
Dunleavey, James M.
Whitworth, Kristin M.
Samuel, Melissa S.
Spate, Lee D.
Cecil, Raissa F.
Benne, Joshua A.
Yan, Xingyu
Fang, Ying
Croix, Brad St.
Lechtenberg, Kelly
Wells, Kevin D.
Prather, Randall S.
author_facet Chen, Paula R.
Rowland, Raymond R. R.
Stoian, Ana M.
Petrovan, Vlad
Sheahan, Maureen
Ganta, Charan
Cino-Ozuna, Giselle
Kim, Dae Young
Dunleavey, James M.
Whitworth, Kristin M.
Samuel, Melissa S.
Spate, Lee D.
Cecil, Raissa F.
Benne, Joshua A.
Yan, Xingyu
Fang, Ying
Croix, Brad St.
Lechtenberg, Kelly
Wells, Kevin D.
Prather, Randall S.
author_sort Chen, Paula R.
collection PubMed
description Senecavirus A (SVA) is a cause of vesicular disease in pigs, and infection rates are rising within the swine industry. Recently, anthrax toxin receptor 1 (ANTXR1) was revealed as the receptor for SVA in human cells. Herein, the role of ANTXR1 as a receptor for SVA in pigs was investigated by CRISPR/Cas9 genome editing. Strikingly, ANTXR1 knockout (KO) pigs exhibited features consistent with the rare disease, GAPO syndrome, in humans. Fibroblasts from wild type (WT) pigs supported replication of SVA; whereas, fibroblasts from KO pigs were resistant to infection. During an SVA challenge, clinical symptoms, including vesicular lesions, and circulating viremia were present in infected WT pigs but were absent in KO pigs. Additional ANTXR1-edited piglets were generated that were homozygous for an in-frame (IF) mutation. While IF pigs presented a GAPO phenotype similar to the KO pigs, fibroblasts showed mild infection, and circulating SVA nucleic acid was decreased in IF compared to WT pigs. Thus, this new ANTXR1 mutation resulted in decreased permissiveness of SVA in pigs. Overall, genetic disruption of ANTXR1 in pigs provides a unique model for GAPO syndrome and prevents circulating SVA infection and clinical symptoms, confirming that ANTXR1 acts as a receptor for the virus.
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spelling pubmed-89431922022-03-28 Disruption of anthrax toxin receptor 1 in pigs leads to a rare disease phenotype and protection from senecavirus A infection Chen, Paula R. Rowland, Raymond R. R. Stoian, Ana M. Petrovan, Vlad Sheahan, Maureen Ganta, Charan Cino-Ozuna, Giselle Kim, Dae Young Dunleavey, James M. Whitworth, Kristin M. Samuel, Melissa S. Spate, Lee D. Cecil, Raissa F. Benne, Joshua A. Yan, Xingyu Fang, Ying Croix, Brad St. Lechtenberg, Kelly Wells, Kevin D. Prather, Randall S. Sci Rep Article Senecavirus A (SVA) is a cause of vesicular disease in pigs, and infection rates are rising within the swine industry. Recently, anthrax toxin receptor 1 (ANTXR1) was revealed as the receptor for SVA in human cells. Herein, the role of ANTXR1 as a receptor for SVA in pigs was investigated by CRISPR/Cas9 genome editing. Strikingly, ANTXR1 knockout (KO) pigs exhibited features consistent with the rare disease, GAPO syndrome, in humans. Fibroblasts from wild type (WT) pigs supported replication of SVA; whereas, fibroblasts from KO pigs were resistant to infection. During an SVA challenge, clinical symptoms, including vesicular lesions, and circulating viremia were present in infected WT pigs but were absent in KO pigs. Additional ANTXR1-edited piglets were generated that were homozygous for an in-frame (IF) mutation. While IF pigs presented a GAPO phenotype similar to the KO pigs, fibroblasts showed mild infection, and circulating SVA nucleic acid was decreased in IF compared to WT pigs. Thus, this new ANTXR1 mutation resulted in decreased permissiveness of SVA in pigs. Overall, genetic disruption of ANTXR1 in pigs provides a unique model for GAPO syndrome and prevents circulating SVA infection and clinical symptoms, confirming that ANTXR1 acts as a receptor for the virus. Nature Publishing Group UK 2022-03-23 /pmc/articles/PMC8943192/ /pubmed/35322150 http://dx.doi.org/10.1038/s41598-022-09123-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Chen, Paula R.
Rowland, Raymond R. R.
Stoian, Ana M.
Petrovan, Vlad
Sheahan, Maureen
Ganta, Charan
Cino-Ozuna, Giselle
Kim, Dae Young
Dunleavey, James M.
Whitworth, Kristin M.
Samuel, Melissa S.
Spate, Lee D.
Cecil, Raissa F.
Benne, Joshua A.
Yan, Xingyu
Fang, Ying
Croix, Brad St.
Lechtenberg, Kelly
Wells, Kevin D.
Prather, Randall S.
Disruption of anthrax toxin receptor 1 in pigs leads to a rare disease phenotype and protection from senecavirus A infection
title Disruption of anthrax toxin receptor 1 in pigs leads to a rare disease phenotype and protection from senecavirus A infection
title_full Disruption of anthrax toxin receptor 1 in pigs leads to a rare disease phenotype and protection from senecavirus A infection
title_fullStr Disruption of anthrax toxin receptor 1 in pigs leads to a rare disease phenotype and protection from senecavirus A infection
title_full_unstemmed Disruption of anthrax toxin receptor 1 in pigs leads to a rare disease phenotype and protection from senecavirus A infection
title_short Disruption of anthrax toxin receptor 1 in pigs leads to a rare disease phenotype and protection from senecavirus A infection
title_sort disruption of anthrax toxin receptor 1 in pigs leads to a rare disease phenotype and protection from senecavirus a infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8943192/
https://www.ncbi.nlm.nih.gov/pubmed/35322150
http://dx.doi.org/10.1038/s41598-022-09123-x
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