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Analysis of Virus and Host Proteomes During Productive HSV-1 and VZV Infection in Human Epithelial Cells

Herpes simplex virus 1 (HSV-1) and varicella-zoster virus (VZV) are two closely related human alphaherpesviruses that persistently infect most adults worldwide and cause a variety of clinically important diseases. Herpesviruses are extremely well adapted to their hosts and interact broadly with cell...

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Autores principales: Ouwendijk, Werner J. D., Dekker, Lennard J. M., van den Ham, Henk-Jan, Lenac Rovis, Tihana, Haefner, Erik S., Jonjic, Stipan, Haas, Jürgen, Luider, Theo M., Verjans, Georges M. G. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7273502/
https://www.ncbi.nlm.nih.gov/pubmed/32547533
http://dx.doi.org/10.3389/fmicb.2020.01179
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author Ouwendijk, Werner J. D.
Dekker, Lennard J. M.
van den Ham, Henk-Jan
Lenac Rovis, Tihana
Haefner, Erik S.
Jonjic, Stipan
Haas, Jürgen
Luider, Theo M.
Verjans, Georges M. G. M.
author_facet Ouwendijk, Werner J. D.
Dekker, Lennard J. M.
van den Ham, Henk-Jan
Lenac Rovis, Tihana
Haefner, Erik S.
Jonjic, Stipan
Haas, Jürgen
Luider, Theo M.
Verjans, Georges M. G. M.
author_sort Ouwendijk, Werner J. D.
collection PubMed
description Herpes simplex virus 1 (HSV-1) and varicella-zoster virus (VZV) are two closely related human alphaherpesviruses that persistently infect most adults worldwide and cause a variety of clinically important diseases. Herpesviruses are extremely well adapted to their hosts and interact broadly with cellular proteins to regulate virus replication and spread. However, it is incompletely understood how HSV-1 and VZV interact with the host proteome during productive infection. This study determined the temporal changes in virus and host protein expression during productive HSV-1 and VZV infection in the same cell type. Results demonstrated the temporally coordinated expression of HSV-1 and VZV proteins in infected cells. Analysis of the host proteomes showed that both viruses affected extracellular matrix composition, transcription, RNA processing and cell division. Moreover, the prominent role of epidermal growth factor receptor (EGFR) signaling during productive HSV-1 and VZV infection was identified. Stimulation and inhibition of EGFR leads to increased and decreased virus replication, respectively. Collectively, the comparative temporal analysis of viral and host proteomes in productively HSV-1 and VZV-infected cells provides a valuable resource for future studies aimed to identify target(s) for antiviral therapy development.
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spelling pubmed-72735022020-06-15 Analysis of Virus and Host Proteomes During Productive HSV-1 and VZV Infection in Human Epithelial Cells Ouwendijk, Werner J. D. Dekker, Lennard J. M. van den Ham, Henk-Jan Lenac Rovis, Tihana Haefner, Erik S. Jonjic, Stipan Haas, Jürgen Luider, Theo M. Verjans, Georges M. G. M. Front Microbiol Microbiology Herpes simplex virus 1 (HSV-1) and varicella-zoster virus (VZV) are two closely related human alphaherpesviruses that persistently infect most adults worldwide and cause a variety of clinically important diseases. Herpesviruses are extremely well adapted to their hosts and interact broadly with cellular proteins to regulate virus replication and spread. However, it is incompletely understood how HSV-1 and VZV interact with the host proteome during productive infection. This study determined the temporal changes in virus and host protein expression during productive HSV-1 and VZV infection in the same cell type. Results demonstrated the temporally coordinated expression of HSV-1 and VZV proteins in infected cells. Analysis of the host proteomes showed that both viruses affected extracellular matrix composition, transcription, RNA processing and cell division. Moreover, the prominent role of epidermal growth factor receptor (EGFR) signaling during productive HSV-1 and VZV infection was identified. Stimulation and inhibition of EGFR leads to increased and decreased virus replication, respectively. Collectively, the comparative temporal analysis of viral and host proteomes in productively HSV-1 and VZV-infected cells provides a valuable resource for future studies aimed to identify target(s) for antiviral therapy development. Frontiers Media S.A. 2020-05-29 /pmc/articles/PMC7273502/ /pubmed/32547533 http://dx.doi.org/10.3389/fmicb.2020.01179 Text en Copyright © 2020 Ouwendijk, Dekker, van den Ham, Lenac Rovis, Haefner, Jonjic, Haas, Luider and Verjans. http://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 Microbiology
Ouwendijk, Werner J. D.
Dekker, Lennard J. M.
van den Ham, Henk-Jan
Lenac Rovis, Tihana
Haefner, Erik S.
Jonjic, Stipan
Haas, Jürgen
Luider, Theo M.
Verjans, Georges M. G. M.
Analysis of Virus and Host Proteomes During Productive HSV-1 and VZV Infection in Human Epithelial Cells
title Analysis of Virus and Host Proteomes During Productive HSV-1 and VZV Infection in Human Epithelial Cells
title_full Analysis of Virus and Host Proteomes During Productive HSV-1 and VZV Infection in Human Epithelial Cells
title_fullStr Analysis of Virus and Host Proteomes During Productive HSV-1 and VZV Infection in Human Epithelial Cells
title_full_unstemmed Analysis of Virus and Host Proteomes During Productive HSV-1 and VZV Infection in Human Epithelial Cells
title_short Analysis of Virus and Host Proteomes During Productive HSV-1 and VZV Infection in Human Epithelial Cells
title_sort analysis of virus and host proteomes during productive hsv-1 and vzv infection in human epithelial cells
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7273502/
https://www.ncbi.nlm.nih.gov/pubmed/32547533
http://dx.doi.org/10.3389/fmicb.2020.01179
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