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Global exploration of the metabolic requirements of gallid alphaherpesvirus 1

Although therapeutics targeting viral metabolic processes have been considered as promising strategies to treat herpesvirus infection, the metabolic requirements of gallid alphaherpesvirus 1 (ILTV), which is economically important to the poultry industry worldwide, remain largely unknown. Using the...

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Autores principales: Qiao, Yangyang, Wang, Zhitao, Han, Zongxi, Shao, Yuhao, Ma, Yong, Liang, Yumeng, Chen, Zhijie, Wu, Hanguang, Cui, Lu, Zhang, Yanhui, Liu, Shengwang, Li, Hai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7470321/
https://www.ncbi.nlm.nih.gov/pubmed/32833996
http://dx.doi.org/10.1371/journal.ppat.1008815
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author Qiao, Yangyang
Wang, Zhitao
Han, Zongxi
Shao, Yuhao
Ma, Yong
Liang, Yumeng
Chen, Zhijie
Wu, Hanguang
Cui, Lu
Zhang, Yanhui
Liu, Shengwang
Li, Hai
author_facet Qiao, Yangyang
Wang, Zhitao
Han, Zongxi
Shao, Yuhao
Ma, Yong
Liang, Yumeng
Chen, Zhijie
Wu, Hanguang
Cui, Lu
Zhang, Yanhui
Liu, Shengwang
Li, Hai
author_sort Qiao, Yangyang
collection PubMed
description Although therapeutics targeting viral metabolic processes have been considered as promising strategies to treat herpesvirus infection, the metabolic requirements of gallid alphaherpesvirus 1 (ILTV), which is economically important to the poultry industry worldwide, remain largely unknown. Using the ILTV-susceptible but nonpermissive chicken cell line DF-1 and the ILTV-permissive chicken cell line LMH as models, the present study explored the metabolic requirements of ILTV by global transcriptome analysis and metabolome assays of ILTV infected cell lines in combination with a set of functional validations. The extensive metabolic exploration demonstrated that ILTV infection tended to promote a metabolic shift from glycolysis to fatty acid (FA) and nucleotide biosynthesis and utilizes glutamine independently of glutaminolysis, without significant general effect on the TCA cycle. In addition, different metabolic pathways were found to be required for distinct stages of ILTV replication. Glucose and glutamine were required for the transcription of viral immediate early gene ICP4 and subsequent steps of viral replication. However, FA synthesis was essential for assembly but not required for other upstream steps of ILTV replication. Moreover, the metabolic requirements of ILTV infection revealed in chicken cell lines were further validated in chicken primary cells isolated from chicken embryo kidneys and chicken embryo livers. The present study, to the best of our knowledge, provides the first global metabolic profile of animal herpesviruses and illustrates the main characteristics of the metabolic program of ILTV.
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spelling pubmed-74703212020-09-11 Global exploration of the metabolic requirements of gallid alphaherpesvirus 1 Qiao, Yangyang Wang, Zhitao Han, Zongxi Shao, Yuhao Ma, Yong Liang, Yumeng Chen, Zhijie Wu, Hanguang Cui, Lu Zhang, Yanhui Liu, Shengwang Li, Hai PLoS Pathog Research Article Although therapeutics targeting viral metabolic processes have been considered as promising strategies to treat herpesvirus infection, the metabolic requirements of gallid alphaherpesvirus 1 (ILTV), which is economically important to the poultry industry worldwide, remain largely unknown. Using the ILTV-susceptible but nonpermissive chicken cell line DF-1 and the ILTV-permissive chicken cell line LMH as models, the present study explored the metabolic requirements of ILTV by global transcriptome analysis and metabolome assays of ILTV infected cell lines in combination with a set of functional validations. The extensive metabolic exploration demonstrated that ILTV infection tended to promote a metabolic shift from glycolysis to fatty acid (FA) and nucleotide biosynthesis and utilizes glutamine independently of glutaminolysis, without significant general effect on the TCA cycle. In addition, different metabolic pathways were found to be required for distinct stages of ILTV replication. Glucose and glutamine were required for the transcription of viral immediate early gene ICP4 and subsequent steps of viral replication. However, FA synthesis was essential for assembly but not required for other upstream steps of ILTV replication. Moreover, the metabolic requirements of ILTV infection revealed in chicken cell lines were further validated in chicken primary cells isolated from chicken embryo kidneys and chicken embryo livers. The present study, to the best of our knowledge, provides the first global metabolic profile of animal herpesviruses and illustrates the main characteristics of the metabolic program of ILTV. Public Library of Science 2020-08-24 /pmc/articles/PMC7470321/ /pubmed/32833996 http://dx.doi.org/10.1371/journal.ppat.1008815 Text en © 2020 Qiao et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Qiao, Yangyang
Wang, Zhitao
Han, Zongxi
Shao, Yuhao
Ma, Yong
Liang, Yumeng
Chen, Zhijie
Wu, Hanguang
Cui, Lu
Zhang, Yanhui
Liu, Shengwang
Li, Hai
Global exploration of the metabolic requirements of gallid alphaherpesvirus 1
title Global exploration of the metabolic requirements of gallid alphaherpesvirus 1
title_full Global exploration of the metabolic requirements of gallid alphaherpesvirus 1
title_fullStr Global exploration of the metabolic requirements of gallid alphaherpesvirus 1
title_full_unstemmed Global exploration of the metabolic requirements of gallid alphaherpesvirus 1
title_short Global exploration of the metabolic requirements of gallid alphaherpesvirus 1
title_sort global exploration of the metabolic requirements of gallid alphaherpesvirus 1
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7470321/
https://www.ncbi.nlm.nih.gov/pubmed/32833996
http://dx.doi.org/10.1371/journal.ppat.1008815
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