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Transcriptomic analysis reveals upregulated host metabolisms and downregulated immune responses or cell death induced by acute African swine fever virus infection

The African swine fever virus is a virulent and communicable viral disease that can be transmitted by infected swine, contaminated pork products, or soft tick vectors. Nonstructural proteins encoded by ASFV regulate viral replication, transcription, and evasion. However, the mechanisms underlying th...

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Autores principales: Cao, Shinuo, Jia, Peng, Wu, Zhi, Lu, Huipeng, Cheng, Yuting, Chen, Changchun, Zhou, Mo, Zhu, Shanyuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10500123/
https://www.ncbi.nlm.nih.gov/pubmed/37720481
http://dx.doi.org/10.3389/fvets.2023.1239926
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author Cao, Shinuo
Jia, Peng
Wu, Zhi
Lu, Huipeng
Cheng, Yuting
Chen, Changchun
Zhou, Mo
Zhu, Shanyuan
author_facet Cao, Shinuo
Jia, Peng
Wu, Zhi
Lu, Huipeng
Cheng, Yuting
Chen, Changchun
Zhou, Mo
Zhu, Shanyuan
author_sort Cao, Shinuo
collection PubMed
description The African swine fever virus is a virulent and communicable viral disease that can be transmitted by infected swine, contaminated pork products, or soft tick vectors. Nonstructural proteins encoded by ASFV regulate viral replication, transcription, and evasion. However, the mechanisms underlying the host response to ASFV infection remain incompletely understood. In order to enhance comprehension of the biology and molecular mechanisms at distinct time intervals (6, 12, 24 h) post infection, transcriptome analyses were executed to discern differentially expressed genes (DEGs) between ASFV and mock-infected PAMs. The transcriptomic analysis unveiled a total of 1,677, 2,122, and 2,945 upregulated DEGs and 933, 1,148, and 1,422 downregulated DEGs in ASFV- and mock-infected groups at 6, 12, and 24 h.p.i.. The results of the transcriptomic analysis demonstrated that the infection of ASFV significantly stimulated host metabolism pathways while concurrently inhibiting the expression of various immune responses and cell death pathways. Our study offers crucial mechanistic insights into the comprehension of ASFV viral pathogenesis and the multifaceted host immune responses. The genes that were dysregulated may serve as potential candidates for further exploration of anti-ASFV strategies.
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spelling pubmed-105001232023-09-15 Transcriptomic analysis reveals upregulated host metabolisms and downregulated immune responses or cell death induced by acute African swine fever virus infection Cao, Shinuo Jia, Peng Wu, Zhi Lu, Huipeng Cheng, Yuting Chen, Changchun Zhou, Mo Zhu, Shanyuan Front Vet Sci Veterinary Science The African swine fever virus is a virulent and communicable viral disease that can be transmitted by infected swine, contaminated pork products, or soft tick vectors. Nonstructural proteins encoded by ASFV regulate viral replication, transcription, and evasion. However, the mechanisms underlying the host response to ASFV infection remain incompletely understood. In order to enhance comprehension of the biology and molecular mechanisms at distinct time intervals (6, 12, 24 h) post infection, transcriptome analyses were executed to discern differentially expressed genes (DEGs) between ASFV and mock-infected PAMs. The transcriptomic analysis unveiled a total of 1,677, 2,122, and 2,945 upregulated DEGs and 933, 1,148, and 1,422 downregulated DEGs in ASFV- and mock-infected groups at 6, 12, and 24 h.p.i.. The results of the transcriptomic analysis demonstrated that the infection of ASFV significantly stimulated host metabolism pathways while concurrently inhibiting the expression of various immune responses and cell death pathways. Our study offers crucial mechanistic insights into the comprehension of ASFV viral pathogenesis and the multifaceted host immune responses. The genes that were dysregulated may serve as potential candidates for further exploration of anti-ASFV strategies. Frontiers Media S.A. 2023-08-31 /pmc/articles/PMC10500123/ /pubmed/37720481 http://dx.doi.org/10.3389/fvets.2023.1239926 Text en Copyright © 2023 Cao, Jia, Wu, Lu, Cheng, Chen, Zhou and Zhu. 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 Veterinary Science
Cao, Shinuo
Jia, Peng
Wu, Zhi
Lu, Huipeng
Cheng, Yuting
Chen, Changchun
Zhou, Mo
Zhu, Shanyuan
Transcriptomic analysis reveals upregulated host metabolisms and downregulated immune responses or cell death induced by acute African swine fever virus infection
title Transcriptomic analysis reveals upregulated host metabolisms and downregulated immune responses or cell death induced by acute African swine fever virus infection
title_full Transcriptomic analysis reveals upregulated host metabolisms and downregulated immune responses or cell death induced by acute African swine fever virus infection
title_fullStr Transcriptomic analysis reveals upregulated host metabolisms and downregulated immune responses or cell death induced by acute African swine fever virus infection
title_full_unstemmed Transcriptomic analysis reveals upregulated host metabolisms and downregulated immune responses or cell death induced by acute African swine fever virus infection
title_short Transcriptomic analysis reveals upregulated host metabolisms and downregulated immune responses or cell death induced by acute African swine fever virus infection
title_sort transcriptomic analysis reveals upregulated host metabolisms and downregulated immune responses or cell death induced by acute african swine fever virus infection
topic Veterinary Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10500123/
https://www.ncbi.nlm.nih.gov/pubmed/37720481
http://dx.doi.org/10.3389/fvets.2023.1239926
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