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Characterization and pathogenicity of a novel variant infectious bursal disease virus in China

Infectious bursal disease (IBD) is a highly epidemic and immunosuppressive disease of 3- to 6-week-old chicks caused by infectious bursal disease virus (IBDV). Since 2017, there has been a notable increase in the isolation rates of novel variant IBDV strains in China, of which characteristic amino a...

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Autores principales: Huang, Yuanling, Shu, Gang, Huang, Cong, Han, Jingyi, Li, Jia, Chen, Hongjun, Chen, Zongyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10064860/
https://www.ncbi.nlm.nih.gov/pubmed/37008302
http://dx.doi.org/10.3389/fmicb.2022.1039259
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author Huang, Yuanling
Shu, Gang
Huang, Cong
Han, Jingyi
Li, Jia
Chen, Hongjun
Chen, Zongyan
author_facet Huang, Yuanling
Shu, Gang
Huang, Cong
Han, Jingyi
Li, Jia
Chen, Hongjun
Chen, Zongyan
author_sort Huang, Yuanling
collection PubMed
description Infectious bursal disease (IBD) is a highly epidemic and immunosuppressive disease of 3- to 6-week-old chicks caused by infectious bursal disease virus (IBDV). Since 2017, there has been a notable increase in the isolation rates of novel variant IBDV strains in China, of which characteristic amino acid residues were different from those of early antigen variants. In this study, one IBDV strain was isolated from a farm with suspected IBD outbreak in Shandong Province, China, which was designated LY21/2. The strain LY21/2 could replicate in MC38 cells with previous culture adaption in SPF chick embryos. Phylogenetic analysis revealed that LY21/2 formed one branch with novel variant IBDVs and shared 96.8–98.6% nucleotide sequence identity with them. Moreover, LY21/2 serving as the major parent underwent the recombination event of a variant strain (19D69), while the minor parent was a very virulent strain (Harbin-1). SPF chicks inoculated with LY21/2 showed no gross clinic symptom, whereas bursal atrophy was exhibited and apoptosis was occurred in 55.21% of bursal cells. The results of histopathology and immunohistochemical staining showed that lymphocyte depletion and connective tissue hyperplasia and IBDV antigen-positive cells were observed in the bursa of LY21/2-infected chicks. Besides, DNA fragmentation was detected in the LY21/2-infected bursal tissue section by TUNEL assay. Collectivtely, these data presented analysis and evaluation of the genetic characteristics and pathogenicity of a novel variant IBDV strain. This study may help in the development of biosafety strategies for the prevention and control of IBDV in poultry.
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spelling pubmed-100648602023-04-01 Characterization and pathogenicity of a novel variant infectious bursal disease virus in China Huang, Yuanling Shu, Gang Huang, Cong Han, Jingyi Li, Jia Chen, Hongjun Chen, Zongyan Front Microbiol Microbiology Infectious bursal disease (IBD) is a highly epidemic and immunosuppressive disease of 3- to 6-week-old chicks caused by infectious bursal disease virus (IBDV). Since 2017, there has been a notable increase in the isolation rates of novel variant IBDV strains in China, of which characteristic amino acid residues were different from those of early antigen variants. In this study, one IBDV strain was isolated from a farm with suspected IBD outbreak in Shandong Province, China, which was designated LY21/2. The strain LY21/2 could replicate in MC38 cells with previous culture adaption in SPF chick embryos. Phylogenetic analysis revealed that LY21/2 formed one branch with novel variant IBDVs and shared 96.8–98.6% nucleotide sequence identity with them. Moreover, LY21/2 serving as the major parent underwent the recombination event of a variant strain (19D69), while the minor parent was a very virulent strain (Harbin-1). SPF chicks inoculated with LY21/2 showed no gross clinic symptom, whereas bursal atrophy was exhibited and apoptosis was occurred in 55.21% of bursal cells. The results of histopathology and immunohistochemical staining showed that lymphocyte depletion and connective tissue hyperplasia and IBDV antigen-positive cells were observed in the bursa of LY21/2-infected chicks. Besides, DNA fragmentation was detected in the LY21/2-infected bursal tissue section by TUNEL assay. Collectivtely, these data presented analysis and evaluation of the genetic characteristics and pathogenicity of a novel variant IBDV strain. This study may help in the development of biosafety strategies for the prevention and control of IBDV in poultry. Frontiers Media S.A. 2023-03-17 /pmc/articles/PMC10064860/ /pubmed/37008302 http://dx.doi.org/10.3389/fmicb.2022.1039259 Text en Copyright © 2023 Huang, Shu, Huang, Han, Li, Chen and Chen. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Huang, Yuanling
Shu, Gang
Huang, Cong
Han, Jingyi
Li, Jia
Chen, Hongjun
Chen, Zongyan
Characterization and pathogenicity of a novel variant infectious bursal disease virus in China
title Characterization and pathogenicity of a novel variant infectious bursal disease virus in China
title_full Characterization and pathogenicity of a novel variant infectious bursal disease virus in China
title_fullStr Characterization and pathogenicity of a novel variant infectious bursal disease virus in China
title_full_unstemmed Characterization and pathogenicity of a novel variant infectious bursal disease virus in China
title_short Characterization and pathogenicity of a novel variant infectious bursal disease virus in China
title_sort characterization and pathogenicity of a novel variant infectious bursal disease virus in china
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10064860/
https://www.ncbi.nlm.nih.gov/pubmed/37008302
http://dx.doi.org/10.3389/fmicb.2022.1039259
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