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Mutations in HPV18 E1^E4 Impact Virus Capsid Assembly, Infectivity Competence, and Maturation

The most highly expressed protein during the productive phase of the human papillomavirus (HPV) life cycle is E1^E4. Its full role during infection remains to be established. HPV E1^E4 is expressed during both the early and late stages of the virus life cycle and contributes to viral genome amplific...

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Autores principales: Biryukov, Jennifer, Myers, Jocelyn C., McLaughlin-Drubin, Margaret E., Griffin, Heather M., Milici, Janice, Doorbar, John, Meyers, Craig
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5744159/
https://www.ncbi.nlm.nih.gov/pubmed/29257050
http://dx.doi.org/10.3390/v9120385
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author Biryukov, Jennifer
Myers, Jocelyn C.
McLaughlin-Drubin, Margaret E.
Griffin, Heather M.
Milici, Janice
Doorbar, John
Meyers, Craig
author_facet Biryukov, Jennifer
Myers, Jocelyn C.
McLaughlin-Drubin, Margaret E.
Griffin, Heather M.
Milici, Janice
Doorbar, John
Meyers, Craig
author_sort Biryukov, Jennifer
collection PubMed
description The most highly expressed protein during the productive phase of the human papillomavirus (HPV) life cycle is E1^E4. Its full role during infection remains to be established. HPV E1^E4 is expressed during both the early and late stages of the virus life cycle and contributes to viral genome amplification. In an attempt to further outline the functions of E1^E4, and determine whether it plays a role in viral capsid assembly and viral infectivity, we examined wild-type E1^E4 as well as four E1^E4 truncation mutants. Our study revealed that HPV18 genomes containing the shortest truncated form of E1^E4, the 17/18 mutant, produced viral titers that were similar to wild-type virus and significantly higher compared to virions containing the three longer E1^E4 mutants. Additionally, the infectivity of virus containing the shortest E1^E4 mutation was equivalent to wild-type and significantly higher than the other three mutants. In contrast, infectivity was completely abrogated for virus containing the longer E1^E4 mutants, regardless of virion maturity. Taken together, our results indicate for the first time that HPV18 E1^E4 impacts capsid assembly and viral infectivity as well as virus maturation.
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spelling pubmed-57441592017-12-31 Mutations in HPV18 E1^E4 Impact Virus Capsid Assembly, Infectivity Competence, and Maturation Biryukov, Jennifer Myers, Jocelyn C. McLaughlin-Drubin, Margaret E. Griffin, Heather M. Milici, Janice Doorbar, John Meyers, Craig Viruses Article The most highly expressed protein during the productive phase of the human papillomavirus (HPV) life cycle is E1^E4. Its full role during infection remains to be established. HPV E1^E4 is expressed during both the early and late stages of the virus life cycle and contributes to viral genome amplification. In an attempt to further outline the functions of E1^E4, and determine whether it plays a role in viral capsid assembly and viral infectivity, we examined wild-type E1^E4 as well as four E1^E4 truncation mutants. Our study revealed that HPV18 genomes containing the shortest truncated form of E1^E4, the 17/18 mutant, produced viral titers that were similar to wild-type virus and significantly higher compared to virions containing the three longer E1^E4 mutants. Additionally, the infectivity of virus containing the shortest E1^E4 mutation was equivalent to wild-type and significantly higher than the other three mutants. In contrast, infectivity was completely abrogated for virus containing the longer E1^E4 mutants, regardless of virion maturity. Taken together, our results indicate for the first time that HPV18 E1^E4 impacts capsid assembly and viral infectivity as well as virus maturation. MDPI 2017-12-19 /pmc/articles/PMC5744159/ /pubmed/29257050 http://dx.doi.org/10.3390/v9120385 Text en © 2017 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
Biryukov, Jennifer
Myers, Jocelyn C.
McLaughlin-Drubin, Margaret E.
Griffin, Heather M.
Milici, Janice
Doorbar, John
Meyers, Craig
Mutations in HPV18 E1^E4 Impact Virus Capsid Assembly, Infectivity Competence, and Maturation
title Mutations in HPV18 E1^E4 Impact Virus Capsid Assembly, Infectivity Competence, and Maturation
title_full Mutations in HPV18 E1^E4 Impact Virus Capsid Assembly, Infectivity Competence, and Maturation
title_fullStr Mutations in HPV18 E1^E4 Impact Virus Capsid Assembly, Infectivity Competence, and Maturation
title_full_unstemmed Mutations in HPV18 E1^E4 Impact Virus Capsid Assembly, Infectivity Competence, and Maturation
title_short Mutations in HPV18 E1^E4 Impact Virus Capsid Assembly, Infectivity Competence, and Maturation
title_sort mutations in hpv18 e1^e4 impact virus capsid assembly, infectivity competence, and maturation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5744159/
https://www.ncbi.nlm.nih.gov/pubmed/29257050
http://dx.doi.org/10.3390/v9120385
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