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Duck Circovirus genotype 2 ORF3 protein induces apoptosis through the mitochondrial pathway

Duck circovirus genotype 2 (DuCV2) belongs to the genus Circovirus, family Circoviridae. It can generally cause lymphocyte atrophy and necrosis in ducks, which leads to immunosuppression. The function of the DuCV2 open reading frame 3 (ORF3) protein in viral pathogenesis in host cells remains unclea...

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Autores principales: Huang, Juan, Zhang, Yanting, Cheng, Anchun, Wang, Mingshu, Liu, Mafeng, Zhu, Dekang, Chen, Shun, Zhao, Xinxin, Yang, Qiao, Wu, Ying, Zhang, Shaqiu, Ou, Xumin, Mao, Sai, Gao, Qun, Sun, Di, Tian, Bin, Yin, Zhongqiong, Jia, Renyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9984893/
https://www.ncbi.nlm.nih.gov/pubmed/36848756
http://dx.doi.org/10.1016/j.psj.2023.102533
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author Huang, Juan
Zhang, Yanting
Cheng, Anchun
Wang, Mingshu
Liu, Mafeng
Zhu, Dekang
Chen, Shun
Zhao, Xinxin
Yang, Qiao
Wu, Ying
Zhang, Shaqiu
Ou, Xumin
Mao, Sai
Gao, Qun
Sun, Di
Tian, Bin
Yin, Zhongqiong
Jia, Renyong
author_facet Huang, Juan
Zhang, Yanting
Cheng, Anchun
Wang, Mingshu
Liu, Mafeng
Zhu, Dekang
Chen, Shun
Zhao, Xinxin
Yang, Qiao
Wu, Ying
Zhang, Shaqiu
Ou, Xumin
Mao, Sai
Gao, Qun
Sun, Di
Tian, Bin
Yin, Zhongqiong
Jia, Renyong
author_sort Huang, Juan
collection PubMed
description Duck circovirus genotype 2 (DuCV2) belongs to the genus Circovirus, family Circoviridae. It can generally cause lymphocyte atrophy and necrosis in ducks, which leads to immunosuppression. The function of the DuCV2 open reading frame 3 (ORF3) protein in viral pathogenesis in host cells remains unclear. Therefore, a series of studies based on ORF3 of the isolate DuCV GH01 strain (belonging to DuCV2) were carried out in duck embryo fibroblasts (DEFs) in this study. The results showed that the ORF3 protein could induce nuclear shrinkage and fragmentation in DEFs. Chromosomal DNA breakage was observed by TUNEL assay. The expression levels of caspase-related genes showed that ORF3 primarily promoted caspase 3 and caspase 9 expression. Furthermore, the protein expression levels of cleaved caspase 3 and cleaved caspase 9 in DEFs were enhanced by ORF3. Thus, ORF3 may activate the mitochondrial apoptosis pathway. When the 20 amino acid residues at the C-terminus of ORF3 (ORF3ΔC(20)) were deleted, the apoptosis rates were decreased. Moreover, compared to ORF3, ORF3ΔC(20) downregulated the mRNA levels of cytochrome c (Cyt c), poly ADP-ribose polymerase (PARP) and apoptosis protease activating factor 1 (Apaf-1), which are the key molecules in the mitochondrial apoptotic pathway. Further study showed that ORF3ΔC(20) could reduce the mitochondrial membrane potential (MMP). This study suggested that the DuCV2 ORF3 protein may primarily activate apoptosis through the mitochondrial pathway in DEFs, and this function is ORF3 C(20) dependent.
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spelling pubmed-99848932023-03-05 Duck Circovirus genotype 2 ORF3 protein induces apoptosis through the mitochondrial pathway Huang, Juan Zhang, Yanting Cheng, Anchun Wang, Mingshu Liu, Mafeng Zhu, Dekang Chen, Shun Zhao, Xinxin Yang, Qiao Wu, Ying Zhang, Shaqiu Ou, Xumin Mao, Sai Gao, Qun Sun, Di Tian, Bin Yin, Zhongqiong Jia, Renyong Poult Sci IMMUNOLOGY, HEALTH AND DISEASE Duck circovirus genotype 2 (DuCV2) belongs to the genus Circovirus, family Circoviridae. It can generally cause lymphocyte atrophy and necrosis in ducks, which leads to immunosuppression. The function of the DuCV2 open reading frame 3 (ORF3) protein in viral pathogenesis in host cells remains unclear. Therefore, a series of studies based on ORF3 of the isolate DuCV GH01 strain (belonging to DuCV2) were carried out in duck embryo fibroblasts (DEFs) in this study. The results showed that the ORF3 protein could induce nuclear shrinkage and fragmentation in DEFs. Chromosomal DNA breakage was observed by TUNEL assay. The expression levels of caspase-related genes showed that ORF3 primarily promoted caspase 3 and caspase 9 expression. Furthermore, the protein expression levels of cleaved caspase 3 and cleaved caspase 9 in DEFs were enhanced by ORF3. Thus, ORF3 may activate the mitochondrial apoptosis pathway. When the 20 amino acid residues at the C-terminus of ORF3 (ORF3ΔC(20)) were deleted, the apoptosis rates were decreased. Moreover, compared to ORF3, ORF3ΔC(20) downregulated the mRNA levels of cytochrome c (Cyt c), poly ADP-ribose polymerase (PARP) and apoptosis protease activating factor 1 (Apaf-1), which are the key molecules in the mitochondrial apoptotic pathway. Further study showed that ORF3ΔC(20) could reduce the mitochondrial membrane potential (MMP). This study suggested that the DuCV2 ORF3 protein may primarily activate apoptosis through the mitochondrial pathway in DEFs, and this function is ORF3 C(20) dependent. Elsevier 2023-01-25 /pmc/articles/PMC9984893/ /pubmed/36848756 http://dx.doi.org/10.1016/j.psj.2023.102533 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle IMMUNOLOGY, HEALTH AND DISEASE
Huang, Juan
Zhang, Yanting
Cheng, Anchun
Wang, Mingshu
Liu, Mafeng
Zhu, Dekang
Chen, Shun
Zhao, Xinxin
Yang, Qiao
Wu, Ying
Zhang, Shaqiu
Ou, Xumin
Mao, Sai
Gao, Qun
Sun, Di
Tian, Bin
Yin, Zhongqiong
Jia, Renyong
Duck Circovirus genotype 2 ORF3 protein induces apoptosis through the mitochondrial pathway
title Duck Circovirus genotype 2 ORF3 protein induces apoptosis through the mitochondrial pathway
title_full Duck Circovirus genotype 2 ORF3 protein induces apoptosis through the mitochondrial pathway
title_fullStr Duck Circovirus genotype 2 ORF3 protein induces apoptosis through the mitochondrial pathway
title_full_unstemmed Duck Circovirus genotype 2 ORF3 protein induces apoptosis through the mitochondrial pathway
title_short Duck Circovirus genotype 2 ORF3 protein induces apoptosis through the mitochondrial pathway
title_sort duck circovirus genotype 2 orf3 protein induces apoptosis through the mitochondrial pathway
topic IMMUNOLOGY, HEALTH AND DISEASE
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9984893/
https://www.ncbi.nlm.nih.gov/pubmed/36848756
http://dx.doi.org/10.1016/j.psj.2023.102533
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