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Epstein-Barr Virus BBRF2 Is Required for Maximum Infectivity

Epstein-Barr virus (EBV) is a member of the gammaherpesvirinae, which causes infectious mononucleosis and several types of cancer. BBRF2 is an uncharacterized gene of EBV and is expressed during the lytic phase. To evaluate its function, BBRF2-knockout EBV was prepared using bacterial artificial chr...

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Autores principales: Masud, H. M. Abdullah Al, Yanagi, Yusuke, Watanabe, Takahiro, Sato, Yoshitaka, Kimura, Hiroshi, Murata, Takayuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6955869/
https://www.ncbi.nlm.nih.gov/pubmed/31888254
http://dx.doi.org/10.3390/microorganisms7120705
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author Masud, H. M. Abdullah Al
Yanagi, Yusuke
Watanabe, Takahiro
Sato, Yoshitaka
Kimura, Hiroshi
Murata, Takayuki
author_facet Masud, H. M. Abdullah Al
Yanagi, Yusuke
Watanabe, Takahiro
Sato, Yoshitaka
Kimura, Hiroshi
Murata, Takayuki
author_sort Masud, H. M. Abdullah Al
collection PubMed
description Epstein-Barr virus (EBV) is a member of the gammaherpesvirinae, which causes infectious mononucleosis and several types of cancer. BBRF2 is an uncharacterized gene of EBV and is expressed during the lytic phase. To evaluate its function, BBRF2-knockout EBV was prepared using bacterial artificial chromosome (BAC) technology and the CRISPR/Cas9 system. Although viral gene expression, DNA synthesis, and progeny secretion were not affected, the infectivity of progeny viruses was significantly reduced by the disruption of BBRF2. When expressed alone, BBRF2 protein localized to the nucleus and cytoplasm, while the coexpression of an interacting partner, BSRF1, resulted in its relocalization to the cytoplasm. Interestingly, the coexpression of BBRF2 protected BSRF1 from proteasome/ubiquitin-dependent degradation. Therefore, BBRF2, together with BSRF1, augments viral infectivity.
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spelling pubmed-69558692020-01-23 Epstein-Barr Virus BBRF2 Is Required for Maximum Infectivity Masud, H. M. Abdullah Al Yanagi, Yusuke Watanabe, Takahiro Sato, Yoshitaka Kimura, Hiroshi Murata, Takayuki Microorganisms Article Epstein-Barr virus (EBV) is a member of the gammaherpesvirinae, which causes infectious mononucleosis and several types of cancer. BBRF2 is an uncharacterized gene of EBV and is expressed during the lytic phase. To evaluate its function, BBRF2-knockout EBV was prepared using bacterial artificial chromosome (BAC) technology and the CRISPR/Cas9 system. Although viral gene expression, DNA synthesis, and progeny secretion were not affected, the infectivity of progeny viruses was significantly reduced by the disruption of BBRF2. When expressed alone, BBRF2 protein localized to the nucleus and cytoplasm, while the coexpression of an interacting partner, BSRF1, resulted in its relocalization to the cytoplasm. Interestingly, the coexpression of BBRF2 protected BSRF1 from proteasome/ubiquitin-dependent degradation. Therefore, BBRF2, together with BSRF1, augments viral infectivity. MDPI 2019-12-16 /pmc/articles/PMC6955869/ /pubmed/31888254 http://dx.doi.org/10.3390/microorganisms7120705 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Masud, H. M. Abdullah Al
Yanagi, Yusuke
Watanabe, Takahiro
Sato, Yoshitaka
Kimura, Hiroshi
Murata, Takayuki
Epstein-Barr Virus BBRF2 Is Required for Maximum Infectivity
title Epstein-Barr Virus BBRF2 Is Required for Maximum Infectivity
title_full Epstein-Barr Virus BBRF2 Is Required for Maximum Infectivity
title_fullStr Epstein-Barr Virus BBRF2 Is Required for Maximum Infectivity
title_full_unstemmed Epstein-Barr Virus BBRF2 Is Required for Maximum Infectivity
title_short Epstein-Barr Virus BBRF2 Is Required for Maximum Infectivity
title_sort epstein-barr virus bbrf2 is required for maximum infectivity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6955869/
https://www.ncbi.nlm.nih.gov/pubmed/31888254
http://dx.doi.org/10.3390/microorganisms7120705
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