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A Novel Variant of Avian Reovirus Is Pathogenic to Vaccinated Chickens
Avian reovirus (ARV) infections, characterized by severe arthritis, tenosynovitis, pericarditis, and poor weight gain, have become increasingly serious in recent years. The economic impact is significant as it causes growth inhibition and immunosuppression. Some commercial poultry in China have been...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10538029/ https://www.ncbi.nlm.nih.gov/pubmed/37766207 http://dx.doi.org/10.3390/v15091800 |
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author | Liu, Rui Luo, Dan Gao, Jinhui Li, Kai Liu, Changjun Qi, Xiaole Cui, Hongyu Zhang, Yanping Wang, Suyan Wang, Xiaomei Gao, Yulong Gao, Li |
author_facet | Liu, Rui Luo, Dan Gao, Jinhui Li, Kai Liu, Changjun Qi, Xiaole Cui, Hongyu Zhang, Yanping Wang, Suyan Wang, Xiaomei Gao, Yulong Gao, Li |
author_sort | Liu, Rui |
collection | PubMed |
description | Avian reovirus (ARV) infections, characterized by severe arthritis, tenosynovitis, pericarditis, and poor weight gain, have become increasingly serious in recent years. The economic impact is significant as it causes growth inhibition and immunosuppression. Some commercial poultry in China have been widely vaccinated with available ARV vaccines; however, infections continue to occur even after vaccination. This study aimed to isolate a novel variant, ARV-SD19/11103, from the joint tissues of infected broiler chickens vaccinated with ARV vaccines in Shandong Province. Genetic evolution analysis of the major protective antigen σC gene in ARVs showed that ARV-SD19/11103 was located in the genotype cluster I but not in the same sub-cluster as the S1133 vaccine strain. The amino acid sequence similarity between SD19/11103 and vaccine strains S1133, 1733, and 2408 was <80%. After analyzing the amino acid sequences of the σC protein, 33 amino acid differences were found between the new variant isolate and the vaccine strains. This novel variant showed obvious pathogenicity in specific pathogen-free chicken embryos and chicks and could cause serious disease in chickens vaccinated with commercially available ARV vaccines. Cross-neutralization experiments further demonstrated a significant antigenic difference between the novel variant and genotype cluster I ARV strains. The novel variant strain isolated in this study provides an important theoretical basis for understanding the prevalence and genetic evolutionary characteristics of ARV variant strains in our country. This study identified the causes of ARVs circulating and emphasizes the needs for developing new vaccines against novel ARV variants. |
format | Online Article Text |
id | pubmed-10538029 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-105380292023-09-29 A Novel Variant of Avian Reovirus Is Pathogenic to Vaccinated Chickens Liu, Rui Luo, Dan Gao, Jinhui Li, Kai Liu, Changjun Qi, Xiaole Cui, Hongyu Zhang, Yanping Wang, Suyan Wang, Xiaomei Gao, Yulong Gao, Li Viruses Article Avian reovirus (ARV) infections, characterized by severe arthritis, tenosynovitis, pericarditis, and poor weight gain, have become increasingly serious in recent years. The economic impact is significant as it causes growth inhibition and immunosuppression. Some commercial poultry in China have been widely vaccinated with available ARV vaccines; however, infections continue to occur even after vaccination. This study aimed to isolate a novel variant, ARV-SD19/11103, from the joint tissues of infected broiler chickens vaccinated with ARV vaccines in Shandong Province. Genetic evolution analysis of the major protective antigen σC gene in ARVs showed that ARV-SD19/11103 was located in the genotype cluster I but not in the same sub-cluster as the S1133 vaccine strain. The amino acid sequence similarity between SD19/11103 and vaccine strains S1133, 1733, and 2408 was <80%. After analyzing the amino acid sequences of the σC protein, 33 amino acid differences were found between the new variant isolate and the vaccine strains. This novel variant showed obvious pathogenicity in specific pathogen-free chicken embryos and chicks and could cause serious disease in chickens vaccinated with commercially available ARV vaccines. Cross-neutralization experiments further demonstrated a significant antigenic difference between the novel variant and genotype cluster I ARV strains. The novel variant strain isolated in this study provides an important theoretical basis for understanding the prevalence and genetic evolutionary characteristics of ARV variant strains in our country. This study identified the causes of ARVs circulating and emphasizes the needs for developing new vaccines against novel ARV variants. MDPI 2023-08-24 /pmc/articles/PMC10538029/ /pubmed/37766207 http://dx.doi.org/10.3390/v15091800 Text en © 2023 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 Liu, Rui Luo, Dan Gao, Jinhui Li, Kai Liu, Changjun Qi, Xiaole Cui, Hongyu Zhang, Yanping Wang, Suyan Wang, Xiaomei Gao, Yulong Gao, Li A Novel Variant of Avian Reovirus Is Pathogenic to Vaccinated Chickens |
title | A Novel Variant of Avian Reovirus Is Pathogenic to Vaccinated Chickens |
title_full | A Novel Variant of Avian Reovirus Is Pathogenic to Vaccinated Chickens |
title_fullStr | A Novel Variant of Avian Reovirus Is Pathogenic to Vaccinated Chickens |
title_full_unstemmed | A Novel Variant of Avian Reovirus Is Pathogenic to Vaccinated Chickens |
title_short | A Novel Variant of Avian Reovirus Is Pathogenic to Vaccinated Chickens |
title_sort | novel variant of avian reovirus is pathogenic to vaccinated chickens |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10538029/ https://www.ncbi.nlm.nih.gov/pubmed/37766207 http://dx.doi.org/10.3390/v15091800 |
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