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Co-Infection with Marek’s Disease Virus and Reticuloendotheliosis Virus Increases Illness Severity and Reduces Marek’s Disease Vaccine Efficacy

Marek’s disease virus (MDV) and reticuloendotheliosis virus (REV) cause Marek’s disease (MD) and reticuloendotheliosis (RE), respectively. Co-infection with MDV and REV is common in chickens, causing serious losses to the poultry industry. However, experimental studies of such co-infection are lacki...

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Autores principales: Sun, Guo-Rong, Zhang, Yan-Ping, Zhou, Lin-Yi, Lv, Hong-Chao, Zhang, Feng, Li, Kai, Gao, Yu-Long, Qi, Xiao-Le, Cui, Hong-Yu, Wang, Yong-Qiang, Gao, Li, Pan, Qing, Wang, Xiao-Mei, Liu, Chang-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5490833/
https://www.ncbi.nlm.nih.gov/pubmed/28635675
http://dx.doi.org/10.3390/v9060158
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author Sun, Guo-Rong
Zhang, Yan-Ping
Zhou, Lin-Yi
Lv, Hong-Chao
Zhang, Feng
Li, Kai
Gao, Yu-Long
Qi, Xiao-Le
Cui, Hong-Yu
Wang, Yong-Qiang
Gao, Li
Pan, Qing
Wang, Xiao-Mei
Liu, Chang-Jun
author_facet Sun, Guo-Rong
Zhang, Yan-Ping
Zhou, Lin-Yi
Lv, Hong-Chao
Zhang, Feng
Li, Kai
Gao, Yu-Long
Qi, Xiao-Le
Cui, Hong-Yu
Wang, Yong-Qiang
Gao, Li
Pan, Qing
Wang, Xiao-Mei
Liu, Chang-Jun
author_sort Sun, Guo-Rong
collection PubMed
description Marek’s disease virus (MDV) and reticuloendotheliosis virus (REV) cause Marek’s disease (MD) and reticuloendotheliosis (RE), respectively. Co-infection with MDV and REV is common in chickens, causing serious losses to the poultry industry. However, experimental studies of such co-infection are lacking. In this study, Chinese field strains of MDV (ZW/15) and REV (JLR1501) were used as challenge viruses to evaluate the pathogenicity of co-infection and the influence of MD vaccination in chickens. Compared to the MDV-challenged group, the mortality and tumor rates increased significantly by 20.0% (76.7 to 96.7%) and 26.7% (53.3 to 80.0%), in the co-challenged group, respectively. The protective index of the MD vaccines CVI988 and 814 decreased by 33.3 (80.0 to 47.7) and 13.3 (90.0 to 76.7), respectively. These results indicated that MDV and REV co-infection significantly increased disease severity and reduced the vaccine efficacy. The MDV genome load showed no difference in the feather pulps and spleen, and pathogenicity-related MDV gene expression (meq, pp38, vIL-8, and ICP4) in the spleen significantly increased at some time points in the co-challenged group. Clearly, synergistic pathogenicity occurred between MDV and REV, and the protective efficacy of existing MD vaccines was attenuated by co-infection with Chinese field MDV and REV strains.
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spelling pubmed-54908332017-06-30 Co-Infection with Marek’s Disease Virus and Reticuloendotheliosis Virus Increases Illness Severity and Reduces Marek’s Disease Vaccine Efficacy Sun, Guo-Rong Zhang, Yan-Ping Zhou, Lin-Yi Lv, Hong-Chao Zhang, Feng Li, Kai Gao, Yu-Long Qi, Xiao-Le Cui, Hong-Yu Wang, Yong-Qiang Gao, Li Pan, Qing Wang, Xiao-Mei Liu, Chang-Jun Viruses Article Marek’s disease virus (MDV) and reticuloendotheliosis virus (REV) cause Marek’s disease (MD) and reticuloendotheliosis (RE), respectively. Co-infection with MDV and REV is common in chickens, causing serious losses to the poultry industry. However, experimental studies of such co-infection are lacking. In this study, Chinese field strains of MDV (ZW/15) and REV (JLR1501) were used as challenge viruses to evaluate the pathogenicity of co-infection and the influence of MD vaccination in chickens. Compared to the MDV-challenged group, the mortality and tumor rates increased significantly by 20.0% (76.7 to 96.7%) and 26.7% (53.3 to 80.0%), in the co-challenged group, respectively. The protective index of the MD vaccines CVI988 and 814 decreased by 33.3 (80.0 to 47.7) and 13.3 (90.0 to 76.7), respectively. These results indicated that MDV and REV co-infection significantly increased disease severity and reduced the vaccine efficacy. The MDV genome load showed no difference in the feather pulps and spleen, and pathogenicity-related MDV gene expression (meq, pp38, vIL-8, and ICP4) in the spleen significantly increased at some time points in the co-challenged group. Clearly, synergistic pathogenicity occurred between MDV and REV, and the protective efficacy of existing MD vaccines was attenuated by co-infection with Chinese field MDV and REV strains. MDPI 2017-06-21 /pmc/articles/PMC5490833/ /pubmed/28635675 http://dx.doi.org/10.3390/v9060158 Text en © 2017 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sun, Guo-Rong
Zhang, Yan-Ping
Zhou, Lin-Yi
Lv, Hong-Chao
Zhang, Feng
Li, Kai
Gao, Yu-Long
Qi, Xiao-Le
Cui, Hong-Yu
Wang, Yong-Qiang
Gao, Li
Pan, Qing
Wang, Xiao-Mei
Liu, Chang-Jun
Co-Infection with Marek’s Disease Virus and Reticuloendotheliosis Virus Increases Illness Severity and Reduces Marek’s Disease Vaccine Efficacy
title Co-Infection with Marek’s Disease Virus and Reticuloendotheliosis Virus Increases Illness Severity and Reduces Marek’s Disease Vaccine Efficacy
title_full Co-Infection with Marek’s Disease Virus and Reticuloendotheliosis Virus Increases Illness Severity and Reduces Marek’s Disease Vaccine Efficacy
title_fullStr Co-Infection with Marek’s Disease Virus and Reticuloendotheliosis Virus Increases Illness Severity and Reduces Marek’s Disease Vaccine Efficacy
title_full_unstemmed Co-Infection with Marek’s Disease Virus and Reticuloendotheliosis Virus Increases Illness Severity and Reduces Marek’s Disease Vaccine Efficacy
title_short Co-Infection with Marek’s Disease Virus and Reticuloendotheliosis Virus Increases Illness Severity and Reduces Marek’s Disease Vaccine Efficacy
title_sort co-infection with marek’s disease virus and reticuloendotheliosis virus increases illness severity and reduces marek’s disease vaccine efficacy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5490833/
https://www.ncbi.nlm.nih.gov/pubmed/28635675
http://dx.doi.org/10.3390/v9060158
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