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Assessment on reticuloendotheliosis virus infection in specific-pathogen-free chickens based on detection of yolk antibody
Reticuloendotheliosis virus (REV) is the most frequent exogenous virus that contaminates attenuated vaccines. Therefore, it is extremely important to select REV-free specific-pathogen-free (SPF) chicken embryos. Generally, REV infection is assessed by detecting REV antibodies in SPF chickens. This p...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6476468/ https://www.ncbi.nlm.nih.gov/pubmed/31009463 http://dx.doi.org/10.1371/journal.pone.0213978 |
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author | Li, Yang Wang, Tuanjie Wang, Lin Sun, Mingjun Cui, Zhizhong Chang, Shuang Wu, Yongping Zhang, Xiaodong Yu, Xiaohui Sun, Tao Zhao, Peng |
author_facet | Li, Yang Wang, Tuanjie Wang, Lin Sun, Mingjun Cui, Zhizhong Chang, Shuang Wu, Yongping Zhang, Xiaodong Yu, Xiaohui Sun, Tao Zhao, Peng |
author_sort | Li, Yang |
collection | PubMed |
description | Reticuloendotheliosis virus (REV) is the most frequent exogenous virus that contaminates attenuated vaccines. Therefore, it is extremely important to select REV-free specific-pathogen-free (SPF) chicken embryos. Generally, REV infection is assessed by detecting REV antibodies in SPF chickens. This present study seeks to evaluate REV infection by replacing serum antibody detection with yolk antibody detection. A cohort of 40 nineteen-week-old SPF chickens were artificially inoculated with REV, with 32 SPF chickens raised in another isolation environment served as a blank control. Eggs and serum from 23-week-old chickens were sampled, and yolks were diluted separately to ratios of 1:150, 1:200, 1:300 and 1:400, which were detected together with serum. We found that the yolk antibody detection findings at a dilution of 1:300 had the highest coincidence rate compared with that based on serum antibody measurements. At a dilution ratio of 1:300 for yolk antibody, 72 chickens were continuously observed for 10 weeks from 25- to 34-weeks-old. Our findings were based on serum antibody or yolk antibody detection, and the evaluation results were completely consistent. Therefore, all serum antibody-positive chickens were yolk antibody-positive, and vice versa. Accordingly, vaccine producers can estimate REV cleanliness in a poultry farm by sampling yolk antibody titers. |
format | Online Article Text |
id | pubmed-6476468 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-64764682019-05-07 Assessment on reticuloendotheliosis virus infection in specific-pathogen-free chickens based on detection of yolk antibody Li, Yang Wang, Tuanjie Wang, Lin Sun, Mingjun Cui, Zhizhong Chang, Shuang Wu, Yongping Zhang, Xiaodong Yu, Xiaohui Sun, Tao Zhao, Peng PLoS One Research Article Reticuloendotheliosis virus (REV) is the most frequent exogenous virus that contaminates attenuated vaccines. Therefore, it is extremely important to select REV-free specific-pathogen-free (SPF) chicken embryos. Generally, REV infection is assessed by detecting REV antibodies in SPF chickens. This present study seeks to evaluate REV infection by replacing serum antibody detection with yolk antibody detection. A cohort of 40 nineteen-week-old SPF chickens were artificially inoculated with REV, with 32 SPF chickens raised in another isolation environment served as a blank control. Eggs and serum from 23-week-old chickens were sampled, and yolks were diluted separately to ratios of 1:150, 1:200, 1:300 and 1:400, which were detected together with serum. We found that the yolk antibody detection findings at a dilution of 1:300 had the highest coincidence rate compared with that based on serum antibody measurements. At a dilution ratio of 1:300 for yolk antibody, 72 chickens were continuously observed for 10 weeks from 25- to 34-weeks-old. Our findings were based on serum antibody or yolk antibody detection, and the evaluation results were completely consistent. Therefore, all serum antibody-positive chickens were yolk antibody-positive, and vice versa. Accordingly, vaccine producers can estimate REV cleanliness in a poultry farm by sampling yolk antibody titers. Public Library of Science 2019-04-22 /pmc/articles/PMC6476468/ /pubmed/31009463 http://dx.doi.org/10.1371/journal.pone.0213978 Text en © 2019 Li et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Li, Yang Wang, Tuanjie Wang, Lin Sun, Mingjun Cui, Zhizhong Chang, Shuang Wu, Yongping Zhang, Xiaodong Yu, Xiaohui Sun, Tao Zhao, Peng Assessment on reticuloendotheliosis virus infection in specific-pathogen-free chickens based on detection of yolk antibody |
title | Assessment on reticuloendotheliosis virus infection in specific-pathogen-free chickens based on detection of yolk antibody |
title_full | Assessment on reticuloendotheliosis virus infection in specific-pathogen-free chickens based on detection of yolk antibody |
title_fullStr | Assessment on reticuloendotheliosis virus infection in specific-pathogen-free chickens based on detection of yolk antibody |
title_full_unstemmed | Assessment on reticuloendotheliosis virus infection in specific-pathogen-free chickens based on detection of yolk antibody |
title_short | Assessment on reticuloendotheliosis virus infection in specific-pathogen-free chickens based on detection of yolk antibody |
title_sort | assessment on reticuloendotheliosis virus infection in specific-pathogen-free chickens based on detection of yolk antibody |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6476468/ https://www.ncbi.nlm.nih.gov/pubmed/31009463 http://dx.doi.org/10.1371/journal.pone.0213978 |
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