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Comparative Analysis of Novel Strains of Porcine Astrovirus Type 3 in the USA
Porcine astrovirus type 3 (PoAstV3) has been previously identified as a cause of polioencephalomyelitis in swine and continues to cause disease in the US swine industry. Herein, we describe the characterization of both untranslated regions, frameshifting signal, putative genome-linked virus protein...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8472076/ https://www.ncbi.nlm.nih.gov/pubmed/34578440 http://dx.doi.org/10.3390/v13091859 |
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author | Matias Ferreyra, Franco Harmon, Karen Bradner, Laura Burrough, Eric Derscheid, Rachel Magstadt, Drew R. Michael, Alyona de Almeida, Marcelo Nunes Schumacher, Loni Siepker, Chris Sitthicharoenchai, Panchan Stevenson, Gregory Arruda, Bailey |
author_facet | Matias Ferreyra, Franco Harmon, Karen Bradner, Laura Burrough, Eric Derscheid, Rachel Magstadt, Drew R. Michael, Alyona de Almeida, Marcelo Nunes Schumacher, Loni Siepker, Chris Sitthicharoenchai, Panchan Stevenson, Gregory Arruda, Bailey |
author_sort | Matias Ferreyra, Franco |
collection | PubMed |
description | Porcine astrovirus type 3 (PoAstV3) has been previously identified as a cause of polioencephalomyelitis in swine and continues to cause disease in the US swine industry. Herein, we describe the characterization of both untranslated regions, frameshifting signal, putative genome-linked virus protein (VPg) and conserved antigenic epitopes of several novel PoAstV3 genomes. Twenty complete coding sequences (CDS) were obtained from 32 diagnostic cases originating from 11 individual farms/systems sharing a nucleotide (amino acid) percent identity of 89.74–100% (94.79–100%), 91.9–100% (96.3–100%) and 90.71–100% (93.51–100%) for ORF1a, ORF1ab and ORF2, respectively. Our results indicate that the 5′UTR of PoAstV3 is highly conserved highlighting the importance of this region in translation initiation while their 3′UTR is moderately conserved among strains, presenting alternative configurations including multiple putative protein binding sites and pseudoknots. Moreover, two predicted conserved antigenic epitopes were identified matching the 3′ termini of VP27 of PoAstV3 USA strains. These epitopes may aid in the design and development of vaccine components and diagnostic assays useful to control outbreaks of PoAstV3-associated CNS disease. In conclusion, this is the first analysis predicting the structure of important regulatory motifs of neurotropic mamastroviruses, which differ from those previously described in human astroviruses. |
format | Online Article Text |
id | pubmed-8472076 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-84720762021-09-28 Comparative Analysis of Novel Strains of Porcine Astrovirus Type 3 in the USA Matias Ferreyra, Franco Harmon, Karen Bradner, Laura Burrough, Eric Derscheid, Rachel Magstadt, Drew R. Michael, Alyona de Almeida, Marcelo Nunes Schumacher, Loni Siepker, Chris Sitthicharoenchai, Panchan Stevenson, Gregory Arruda, Bailey Viruses Article Porcine astrovirus type 3 (PoAstV3) has been previously identified as a cause of polioencephalomyelitis in swine and continues to cause disease in the US swine industry. Herein, we describe the characterization of both untranslated regions, frameshifting signal, putative genome-linked virus protein (VPg) and conserved antigenic epitopes of several novel PoAstV3 genomes. Twenty complete coding sequences (CDS) were obtained from 32 diagnostic cases originating from 11 individual farms/systems sharing a nucleotide (amino acid) percent identity of 89.74–100% (94.79–100%), 91.9–100% (96.3–100%) and 90.71–100% (93.51–100%) for ORF1a, ORF1ab and ORF2, respectively. Our results indicate that the 5′UTR of PoAstV3 is highly conserved highlighting the importance of this region in translation initiation while their 3′UTR is moderately conserved among strains, presenting alternative configurations including multiple putative protein binding sites and pseudoknots. Moreover, two predicted conserved antigenic epitopes were identified matching the 3′ termini of VP27 of PoAstV3 USA strains. These epitopes may aid in the design and development of vaccine components and diagnostic assays useful to control outbreaks of PoAstV3-associated CNS disease. In conclusion, this is the first analysis predicting the structure of important regulatory motifs of neurotropic mamastroviruses, which differ from those previously described in human astroviruses. MDPI 2021-09-17 /pmc/articles/PMC8472076/ /pubmed/34578440 http://dx.doi.org/10.3390/v13091859 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Matias Ferreyra, Franco Harmon, Karen Bradner, Laura Burrough, Eric Derscheid, Rachel Magstadt, Drew R. Michael, Alyona de Almeida, Marcelo Nunes Schumacher, Loni Siepker, Chris Sitthicharoenchai, Panchan Stevenson, Gregory Arruda, Bailey Comparative Analysis of Novel Strains of Porcine Astrovirus Type 3 in the USA |
title | Comparative Analysis of Novel Strains of Porcine Astrovirus Type 3 in the USA |
title_full | Comparative Analysis of Novel Strains of Porcine Astrovirus Type 3 in the USA |
title_fullStr | Comparative Analysis of Novel Strains of Porcine Astrovirus Type 3 in the USA |
title_full_unstemmed | Comparative Analysis of Novel Strains of Porcine Astrovirus Type 3 in the USA |
title_short | Comparative Analysis of Novel Strains of Porcine Astrovirus Type 3 in the USA |
title_sort | comparative analysis of novel strains of porcine astrovirus type 3 in the usa |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8472076/ https://www.ncbi.nlm.nih.gov/pubmed/34578440 http://dx.doi.org/10.3390/v13091859 |
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