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Apoptosis induced in vivo by new type gosling viral enteritis virus

In this study, apoptosis was induced by new type gosling viral enteritis virus (NGVEV) in experimentally infected goslings is reported in detail for the first time. After 3-day-old goslings were orally inoculated with a NGVEV-CN strain suspension, the time course of NGVEV effects on apoptotic morpho...

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Autores principales: Chen, Shun, Cheng, Anchun, Wang, Mingshu, Zhu, Dekang, Jia, Renyong, Luo, Qihui, Cui, Hengmin, Zhou, Yi, Wang, Yin, Xu, Zhiwen, Chen, Zhengli, Chen, Xiaoyue, Wang, Xiaoyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Veterinary Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3232392/
https://www.ncbi.nlm.nih.gov/pubmed/22122899
http://dx.doi.org/10.4142/jvs.2011.12.4.333
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author Chen, Shun
Cheng, Anchun
Wang, Mingshu
Zhu, Dekang
Jia, Renyong
Luo, Qihui
Cui, Hengmin
Zhou, Yi
Wang, Yin
Xu, Zhiwen
Chen, Zhengli
Chen, Xiaoyue
Wang, Xiaoyu
author_facet Chen, Shun
Cheng, Anchun
Wang, Mingshu
Zhu, Dekang
Jia, Renyong
Luo, Qihui
Cui, Hengmin
Zhou, Yi
Wang, Yin
Xu, Zhiwen
Chen, Zhengli
Chen, Xiaoyue
Wang, Xiaoyu
author_sort Chen, Shun
collection PubMed
description In this study, apoptosis was induced by new type gosling viral enteritis virus (NGVEV) in experimentally infected goslings is reported in detail for the first time. After 3-day-old goslings were orally inoculated with a NGVEV-CN strain suspension, the time course of NGVEV effects on apoptotic morphological changes of the internal tissues was evaluated. These changes were observed by histological analysis with light microscopy and ultrastructural analysis with transmission electron microscopy. DNA fragmentation was assessed with a terminal deoxynucleotidyl transferase-mediated dUTP nick end-labeling (TUNEL) assay and DNA ladder analysis. A series of characteristic apoptotic morphological changes including chromatin condensation and margination, cytoplasmic shrinkage, plasma membrane blebbing, and formation of apoptotic bodies were noted. Apoptosis was readily observed in the lymphoid and gastrointestinal organs, and sporadically occurred in other organs after 3 days post-infection (PI). The presence and quantity of TUNEL-positive cells increased with infection time until 9 days PI. DNA extracted from the NGVEV-infected gosling cells displayed characteristic 180~200 bp ladders. Apoptotic cells were ubiquitously distributed, especially among lymphocytes, macrophages, monocytes, and epithelial and intestinal cells. Necrosis was subsequently detected during the late NGVEV-infection phase, which was characterized by cell swelling, plasma membrane collapse, and rapidly lysis. Our results suggested that apoptosis may play an important role in the pathogenesis of NGVE disease.
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spelling pubmed-32323922011-12-08 Apoptosis induced in vivo by new type gosling viral enteritis virus Chen, Shun Cheng, Anchun Wang, Mingshu Zhu, Dekang Jia, Renyong Luo, Qihui Cui, Hengmin Zhou, Yi Wang, Yin Xu, Zhiwen Chen, Zhengli Chen, Xiaoyue Wang, Xiaoyu J Vet Sci Original Article In this study, apoptosis was induced by new type gosling viral enteritis virus (NGVEV) in experimentally infected goslings is reported in detail for the first time. After 3-day-old goslings were orally inoculated with a NGVEV-CN strain suspension, the time course of NGVEV effects on apoptotic morphological changes of the internal tissues was evaluated. These changes were observed by histological analysis with light microscopy and ultrastructural analysis with transmission electron microscopy. DNA fragmentation was assessed with a terminal deoxynucleotidyl transferase-mediated dUTP nick end-labeling (TUNEL) assay and DNA ladder analysis. A series of characteristic apoptotic morphological changes including chromatin condensation and margination, cytoplasmic shrinkage, plasma membrane blebbing, and formation of apoptotic bodies were noted. Apoptosis was readily observed in the lymphoid and gastrointestinal organs, and sporadically occurred in other organs after 3 days post-infection (PI). The presence and quantity of TUNEL-positive cells increased with infection time until 9 days PI. DNA extracted from the NGVEV-infected gosling cells displayed characteristic 180~200 bp ladders. Apoptotic cells were ubiquitously distributed, especially among lymphocytes, macrophages, monocytes, and epithelial and intestinal cells. Necrosis was subsequently detected during the late NGVEV-infection phase, which was characterized by cell swelling, plasma membrane collapse, and rapidly lysis. Our results suggested that apoptosis may play an important role in the pathogenesis of NGVE disease. The Korean Society of Veterinary Science 2011-12 2011-11-30 /pmc/articles/PMC3232392/ /pubmed/22122899 http://dx.doi.org/10.4142/jvs.2011.12.4.333 Text en Copyright © 2011 The Korean Society of Veterinary Science https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Chen, Shun
Cheng, Anchun
Wang, Mingshu
Zhu, Dekang
Jia, Renyong
Luo, Qihui
Cui, Hengmin
Zhou, Yi
Wang, Yin
Xu, Zhiwen
Chen, Zhengli
Chen, Xiaoyue
Wang, Xiaoyu
Apoptosis induced in vivo by new type gosling viral enteritis virus
title Apoptosis induced in vivo by new type gosling viral enteritis virus
title_full Apoptosis induced in vivo by new type gosling viral enteritis virus
title_fullStr Apoptosis induced in vivo by new type gosling viral enteritis virus
title_full_unstemmed Apoptosis induced in vivo by new type gosling viral enteritis virus
title_short Apoptosis induced in vivo by new type gosling viral enteritis virus
title_sort apoptosis induced in vivo by new type gosling viral enteritis virus
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3232392/
https://www.ncbi.nlm.nih.gov/pubmed/22122899
http://dx.doi.org/10.4142/jvs.2011.12.4.333
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