Establishment of Human Papillomavirus Infection Requires Cell Cycle Progression: e1000318
Human papillomaviruses (HPVs) are DNA viruses associated with major human cancers. As such there is a strong interest in developing new means, such as vaccines and microbicides, to prevent HPV infections. Developing the latter requires a better understanding of the infectious life cycle of HPVs. The...
Gespeichert in:
Veröffentlicht in: | PLoS pathogens 2009-02, Vol.5 (2) |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | 2 |
container_start_page | |
container_title | PLoS pathogens |
container_volume | 5 |
creator | Pyeon, Dohun Pearce, Shane M Lank, Simon M Ahlquist, Paul Lambert, Paul F |
description | Human papillomaviruses (HPVs) are DNA viruses associated with major human cancers. As such there is a strong interest in developing new means, such as vaccines and microbicides, to prevent HPV infections. Developing the latter requires a better understanding of the infectious life cycle of HPVs. The HPV infectious life cycle is closely linked to the differentiation state of the stratified epithelium it infects, with progeny virus only made in the terminally differentiating suprabasal compartment. It has long been recognized that HPV must first establish its infection within the basal layer of stratified epithelium, but why this is the case has not been understood. In part this restriction might reflect specificity of expression of entry receptors. However, this hypothesis could not fully explain the differentiation restriction of HPV infection, since many cell types can be infected with HPVs in monolayer cell culture. Here, we used chemical biology approaches to reveal that cell cycle progression through mitosis is critical for HPV infection. Using infectious HPV16 particles containing the intact viral genome, G1-synchronized human keratinocytes as hosts, and early viral gene expression as a readout for infection, we learned that the recipient cell must enter M phase (mitosis) for HPV infection to take place. Late M phase inhibitors had no effect on infection, whereas G1, S, G2, and early M phase cell cycle inhibitors efficiently prevented infection. We conclude that host cells need to pass through early prophase for successful onset of transcription of the HPV encapsidated genes. These findings provide one reason why HPVs initially establish infections in the basal compartment of stratified epithelia. Only this compartment of the epithelium contains cells progressing through the cell cycle, and therefore it is only in these cells that HPVs can establish their infection. By defining a major condition for cell susceptibility to HPV infection, these results also have potentially important implications for HPV control. |
doi_str_mv | 10.1371/journal.ppat.1000318 |
format | Article |
fullrecord | <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_journals_1289051853</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2896511401</sourcerecordid><originalsourceid>FETCH-proquest_journals_12890518533</originalsourceid><addsrcrecordid>eNqNjr0KwjAYRYMo-PsGDgHn1nzG_jgXpU6KuEuUVCNpUvMlgm9vh-LsdC_nnuESMgcWA89g-bTBGaHjphE-BsYYh7xHRpAkPMp4tu7_epoOyRjxydgaOKQjctiiF1et8FFL46mtaBlqYehRNEprW4u3cgHp3lTy5pU19CRfQTmJtJBa0-Jz05Ienb23CNt9SgaV0ChnXU7IYrc9F2XUOPsKEv2lO4sXWOUblkCecP6f9QWDvkhw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1289051853</pqid></control><display><type>article</type><title>Establishment of Human Papillomavirus Infection Requires Cell Cycle Progression: e1000318</title><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central Open Access</source><source>Public Library of Science (PLoS)</source><source>PubMed Central</source><creator>Pyeon, Dohun ; Pearce, Shane M ; Lank, Simon M ; Ahlquist, Paul ; Lambert, Paul F</creator><creatorcontrib>Pyeon, Dohun ; Pearce, Shane M ; Lank, Simon M ; Ahlquist, Paul ; Lambert, Paul F</creatorcontrib><description>Human papillomaviruses (HPVs) are DNA viruses associated with major human cancers. As such there is a strong interest in developing new means, such as vaccines and microbicides, to prevent HPV infections. Developing the latter requires a better understanding of the infectious life cycle of HPVs. The HPV infectious life cycle is closely linked to the differentiation state of the stratified epithelium it infects, with progeny virus only made in the terminally differentiating suprabasal compartment. It has long been recognized that HPV must first establish its infection within the basal layer of stratified epithelium, but why this is the case has not been understood. In part this restriction might reflect specificity of expression of entry receptors. However, this hypothesis could not fully explain the differentiation restriction of HPV infection, since many cell types can be infected with HPVs in monolayer cell culture. Here, we used chemical biology approaches to reveal that cell cycle progression through mitosis is critical for HPV infection. Using infectious HPV16 particles containing the intact viral genome, G1-synchronized human keratinocytes as hosts, and early viral gene expression as a readout for infection, we learned that the recipient cell must enter M phase (mitosis) for HPV infection to take place. Late M phase inhibitors had no effect on infection, whereas G1, S, G2, and early M phase cell cycle inhibitors efficiently prevented infection. We conclude that host cells need to pass through early prophase for successful onset of transcription of the HPV encapsidated genes. These findings provide one reason why HPVs initially establish infections in the basal compartment of stratified epithelia. Only this compartment of the epithelium contains cells progressing through the cell cycle, and therefore it is only in these cells that HPVs can establish their infection. By defining a major condition for cell susceptibility to HPV infection, these results also have potentially important implications for HPV control.</description><identifier>ISSN: 1553-7366</identifier><identifier>EISSN: 1553-7374</identifier><identifier>DOI: 10.1371/journal.ppat.1000318</identifier><language>eng</language><publisher>San Francisco: Public Library of Science</publisher><subject>Cell culture ; Cell cycle ; Cervical cancer ; Colleges & universities ; Genomes ; Head & neck cancer ; Human papillomavirus ; Infections ; Sexually transmitted diseases ; STD</subject><ispartof>PLoS pathogens, 2009-02, Vol.5 (2)</ispartof><rights>2009 Pyeon et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Pyeon D, Pearce SM, Lank SM, Ahlquist P, Lambert PF (2009) Establishment of Human Papillomavirus Infection Requires Cell Cycle Progression. PLoS Pathog 5(2): e1000318. doi:10.1371/journal.ppat.1000318</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,862,27907,27908</link.rule.ids></links><search><creatorcontrib>Pyeon, Dohun</creatorcontrib><creatorcontrib>Pearce, Shane M</creatorcontrib><creatorcontrib>Lank, Simon M</creatorcontrib><creatorcontrib>Ahlquist, Paul</creatorcontrib><creatorcontrib>Lambert, Paul F</creatorcontrib><title>Establishment of Human Papillomavirus Infection Requires Cell Cycle Progression: e1000318</title><title>PLoS pathogens</title><description>Human papillomaviruses (HPVs) are DNA viruses associated with major human cancers. As such there is a strong interest in developing new means, such as vaccines and microbicides, to prevent HPV infections. Developing the latter requires a better understanding of the infectious life cycle of HPVs. The HPV infectious life cycle is closely linked to the differentiation state of the stratified epithelium it infects, with progeny virus only made in the terminally differentiating suprabasal compartment. It has long been recognized that HPV must first establish its infection within the basal layer of stratified epithelium, but why this is the case has not been understood. In part this restriction might reflect specificity of expression of entry receptors. However, this hypothesis could not fully explain the differentiation restriction of HPV infection, since many cell types can be infected with HPVs in monolayer cell culture. Here, we used chemical biology approaches to reveal that cell cycle progression through mitosis is critical for HPV infection. Using infectious HPV16 particles containing the intact viral genome, G1-synchronized human keratinocytes as hosts, and early viral gene expression as a readout for infection, we learned that the recipient cell must enter M phase (mitosis) for HPV infection to take place. Late M phase inhibitors had no effect on infection, whereas G1, S, G2, and early M phase cell cycle inhibitors efficiently prevented infection. We conclude that host cells need to pass through early prophase for successful onset of transcription of the HPV encapsidated genes. These findings provide one reason why HPVs initially establish infections in the basal compartment of stratified epithelia. Only this compartment of the epithelium contains cells progressing through the cell cycle, and therefore it is only in these cells that HPVs can establish their infection. By defining a major condition for cell susceptibility to HPV infection, these results also have potentially important implications for HPV control.</description><subject>Cell culture</subject><subject>Cell cycle</subject><subject>Cervical cancer</subject><subject>Colleges & universities</subject><subject>Genomes</subject><subject>Head & neck cancer</subject><subject>Human papillomavirus</subject><subject>Infections</subject><subject>Sexually transmitted diseases</subject><subject>STD</subject><issn>1553-7366</issn><issn>1553-7374</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNjr0KwjAYRYMo-PsGDgHn1nzG_jgXpU6KuEuUVCNpUvMlgm9vh-LsdC_nnuESMgcWA89g-bTBGaHjphE-BsYYh7xHRpAkPMp4tu7_epoOyRjxydgaOKQjctiiF1et8FFL46mtaBlqYehRNEprW4u3cgHp3lTy5pU19CRfQTmJtJBa0-Jz05Ienb23CNt9SgaV0ChnXU7IYrc9F2XUOPsKEv2lO4sXWOUblkCecP6f9QWDvkhw</recordid><startdate>20090201</startdate><enddate>20090201</enddate><creator>Pyeon, Dohun</creator><creator>Pearce, Shane M</creator><creator>Lank, Simon M</creator><creator>Ahlquist, Paul</creator><creator>Lambert, Paul F</creator><general>Public Library of Science</general><scope>3V.</scope><scope>7QL</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20090201</creationdate><title>Establishment of Human Papillomavirus Infection Requires Cell Cycle Progression</title><author>Pyeon, Dohun ; Pearce, Shane M ; Lank, Simon M ; Ahlquist, Paul ; Lambert, Paul F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_12890518533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Cell culture</topic><topic>Cell cycle</topic><topic>Cervical cancer</topic><topic>Colleges & universities</topic><topic>Genomes</topic><topic>Head & neck cancer</topic><topic>Human papillomavirus</topic><topic>Infections</topic><topic>Sexually transmitted diseases</topic><topic>STD</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pyeon, Dohun</creatorcontrib><creatorcontrib>Pearce, Shane M</creatorcontrib><creatorcontrib>Lank, Simon M</creatorcontrib><creatorcontrib>Ahlquist, Paul</creatorcontrib><creatorcontrib>Lambert, Paul F</creatorcontrib><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>PLoS pathogens</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pyeon, Dohun</au><au>Pearce, Shane M</au><au>Lank, Simon M</au><au>Ahlquist, Paul</au><au>Lambert, Paul F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Establishment of Human Papillomavirus Infection Requires Cell Cycle Progression: e1000318</atitle><jtitle>PLoS pathogens</jtitle><date>2009-02-01</date><risdate>2009</risdate><volume>5</volume><issue>2</issue><issn>1553-7366</issn><eissn>1553-7374</eissn><abstract>Human papillomaviruses (HPVs) are DNA viruses associated with major human cancers. As such there is a strong interest in developing new means, such as vaccines and microbicides, to prevent HPV infections. Developing the latter requires a better understanding of the infectious life cycle of HPVs. The HPV infectious life cycle is closely linked to the differentiation state of the stratified epithelium it infects, with progeny virus only made in the terminally differentiating suprabasal compartment. It has long been recognized that HPV must first establish its infection within the basal layer of stratified epithelium, but why this is the case has not been understood. In part this restriction might reflect specificity of expression of entry receptors. However, this hypothesis could not fully explain the differentiation restriction of HPV infection, since many cell types can be infected with HPVs in monolayer cell culture. Here, we used chemical biology approaches to reveal that cell cycle progression through mitosis is critical for HPV infection. Using infectious HPV16 particles containing the intact viral genome, G1-synchronized human keratinocytes as hosts, and early viral gene expression as a readout for infection, we learned that the recipient cell must enter M phase (mitosis) for HPV infection to take place. Late M phase inhibitors had no effect on infection, whereas G1, S, G2, and early M phase cell cycle inhibitors efficiently prevented infection. We conclude that host cells need to pass through early prophase for successful onset of transcription of the HPV encapsidated genes. These findings provide one reason why HPVs initially establish infections in the basal compartment of stratified epithelia. Only this compartment of the epithelium contains cells progressing through the cell cycle, and therefore it is only in these cells that HPVs can establish their infection. By defining a major condition for cell susceptibility to HPV infection, these results also have potentially important implications for HPV control.</abstract><cop>San Francisco</cop><pub>Public Library of Science</pub><doi>10.1371/journal.ppat.1000318</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1553-7366 |
ispartof | PLoS pathogens, 2009-02, Vol.5 (2) |
issn | 1553-7366 1553-7374 |
language | eng |
recordid | cdi_proquest_journals_1289051853 |
source | DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central Open Access; Public Library of Science (PLoS); PubMed Central |
subjects | Cell culture Cell cycle Cervical cancer Colleges & universities Genomes Head & neck cancer Human papillomavirus Infections Sexually transmitted diseases STD |
title | Establishment of Human Papillomavirus Infection Requires Cell Cycle Progression: e1000318 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-16T20%3A18%3A02IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Establishment%20of%20Human%20Papillomavirus%20Infection%20Requires%20Cell%20Cycle%20Progression:%20e1000318&rft.jtitle=PLoS%20pathogens&rft.au=Pyeon,%20Dohun&rft.date=2009-02-01&rft.volume=5&rft.issue=2&rft.issn=1553-7366&rft.eissn=1553-7374&rft_id=info:doi/10.1371/journal.ppat.1000318&rft_dat=%3Cproquest%3E2896511401%3C/proquest%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1289051853&rft_id=info:pmid/&rfr_iscdi=true |