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Metabolomic analysis of porcine intestinal epithelial cells during swine acute diarrhea syndrome coronavirus infection

Swine acute diarrhea syndrome coronavirus (SADS-CoV) is an enveloped, positive single-stranded RNA virus belonging to Coronaviridae family, Orthocoronavirinae subfamily, Alphacoronavirus genus. As one of the main causes of swine diarrhea, SADS-CoV has brought huge losses to the pig industry. Althoug...

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Autores principales: Zeng, Siying, Peng, Ouyang, Hu, Fangyu, Xia, Yu, Geng, Rui, Zhao, Yan, He, Yihong, Xu, Qiuping, Xue, Chunyi, Cao, Yongchang, Zhang, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9751206/
https://www.ncbi.nlm.nih.gov/pubmed/36530441
http://dx.doi.org/10.3389/fcimb.2022.1079297
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author Zeng, Siying
Peng, Ouyang
Hu, Fangyu
Xia, Yu
Geng, Rui
Zhao, Yan
He, Yihong
Xu, Qiuping
Xue, Chunyi
Cao, Yongchang
Zhang, Hao
author_facet Zeng, Siying
Peng, Ouyang
Hu, Fangyu
Xia, Yu
Geng, Rui
Zhao, Yan
He, Yihong
Xu, Qiuping
Xue, Chunyi
Cao, Yongchang
Zhang, Hao
author_sort Zeng, Siying
collection PubMed
description Swine acute diarrhea syndrome coronavirus (SADS-CoV) is an enveloped, positive single-stranded RNA virus belonging to Coronaviridae family, Orthocoronavirinae subfamily, Alphacoronavirus genus. As one of the main causes of swine diarrhea, SADS-CoV has brought huge losses to the pig industry. Although we have a basic understanding of SADS-CoV, the research on the pathogenicity and interactions between host and virus are still limited, especially the metabolic changes induced by SADS-CoV infection. Here, we utilized a combination of untargeted metabolomics and lipomics to analyze the metabolic alteration in SADS-CoV infected cells. Significant changes were observed in 1257 of 2225 metabolites identified in untargeted metabolomics, while the number of lipomics was 435 out of 868. Metabolic pathway enrichment analysis showed that amino acid metabolism, tricarboxylic acid (TCA) cycle and ferroptosis were disrupted during viral infection, suggesting that these metabolic pathways may partake in pathological processes related to SADS-CoV pathogenesis. Collectively, our findings gain insights into the cellular metabolic disorder during SADS-CoV infection, offer a valuable resource for further exploration of the relationship between virus and host metabolic activities, and provide potential targets for the development of antiviral drugs.
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spelling pubmed-97512062022-12-16 Metabolomic analysis of porcine intestinal epithelial cells during swine acute diarrhea syndrome coronavirus infection Zeng, Siying Peng, Ouyang Hu, Fangyu Xia, Yu Geng, Rui Zhao, Yan He, Yihong Xu, Qiuping Xue, Chunyi Cao, Yongchang Zhang, Hao Front Cell Infect Microbiol Cellular and Infection Microbiology Swine acute diarrhea syndrome coronavirus (SADS-CoV) is an enveloped, positive single-stranded RNA virus belonging to Coronaviridae family, Orthocoronavirinae subfamily, Alphacoronavirus genus. As one of the main causes of swine diarrhea, SADS-CoV has brought huge losses to the pig industry. Although we have a basic understanding of SADS-CoV, the research on the pathogenicity and interactions between host and virus are still limited, especially the metabolic changes induced by SADS-CoV infection. Here, we utilized a combination of untargeted metabolomics and lipomics to analyze the metabolic alteration in SADS-CoV infected cells. Significant changes were observed in 1257 of 2225 metabolites identified in untargeted metabolomics, while the number of lipomics was 435 out of 868. Metabolic pathway enrichment analysis showed that amino acid metabolism, tricarboxylic acid (TCA) cycle and ferroptosis were disrupted during viral infection, suggesting that these metabolic pathways may partake in pathological processes related to SADS-CoV pathogenesis. Collectively, our findings gain insights into the cellular metabolic disorder during SADS-CoV infection, offer a valuable resource for further exploration of the relationship between virus and host metabolic activities, and provide potential targets for the development of antiviral drugs. Frontiers Media S.A. 2022-12-01 /pmc/articles/PMC9751206/ /pubmed/36530441 http://dx.doi.org/10.3389/fcimb.2022.1079297 Text en Copyright © 2022 Zeng, Peng, Hu, Xia, Geng, Zhao, He, Xu, Xue, Cao and Zhang 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 Cellular and Infection Microbiology
Zeng, Siying
Peng, Ouyang
Hu, Fangyu
Xia, Yu
Geng, Rui
Zhao, Yan
He, Yihong
Xu, Qiuping
Xue, Chunyi
Cao, Yongchang
Zhang, Hao
Metabolomic analysis of porcine intestinal epithelial cells during swine acute diarrhea syndrome coronavirus infection
title Metabolomic analysis of porcine intestinal epithelial cells during swine acute diarrhea syndrome coronavirus infection
title_full Metabolomic analysis of porcine intestinal epithelial cells during swine acute diarrhea syndrome coronavirus infection
title_fullStr Metabolomic analysis of porcine intestinal epithelial cells during swine acute diarrhea syndrome coronavirus infection
title_full_unstemmed Metabolomic analysis of porcine intestinal epithelial cells during swine acute diarrhea syndrome coronavirus infection
title_short Metabolomic analysis of porcine intestinal epithelial cells during swine acute diarrhea syndrome coronavirus infection
title_sort metabolomic analysis of porcine intestinal epithelial cells during swine acute diarrhea syndrome coronavirus infection
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9751206/
https://www.ncbi.nlm.nih.gov/pubmed/36530441
http://dx.doi.org/10.3389/fcimb.2022.1079297
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