author_facet Funk, Anneke
Mhamdi, Mouna
Lin, Li
Will, Hans
Sirma, Hüseyin
Funk, Anneke
Mhamdi, Mouna
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author Funk, Anneke
Mhamdi, Mouna
Lin, Li
Will, Hans
Sirma, Hüseyin
spellingShingle Funk, Anneke
Mhamdi, Mouna
Lin, Li
Will, Hans
Sirma, Hüseyin
Journal of Virology
Itinerary of Hepatitis B Viruses: Delineation of Restriction Points Critical for Infectious Entry
Virology
Insect Science
Immunology
Microbiology
author_sort funk, anneke
spelling Funk, Anneke Mhamdi, Mouna Lin, Li Will, Hans Sirma, Hüseyin 0022-538X 1098-5514 American Society for Microbiology Virology Insect Science Immunology Microbiology http://dx.doi.org/10.1128/jvi.78.15.8289-8300.2004 <jats:title>ABSTRACT</jats:title> <jats:p> Little is known about cellular determinants essential for human hepatitis B virus infection. Using the duck hepatitis B virus as a model, we first established a sensitive binding assay for both virions and subviral particles and subsequently elucidated the characteristics of the early viral entry steps. The infection itinerary was found to initiate with the attachment of viral particles to a low number of binding sites on hepatocytes (about 10 <jats:sup>4</jats:sup> per cell). Virus internalization was fully accomplished in less than 3 h but was then followed by a period of unprecedented length, about 14 h, until completion of nuclear import of the viral genome. Steps subsequent to virus entry depended on both intact microtubules and their dynamic turnover but not on actin cytoskeleton. Notably, cytoplasmic trafficking of viral particles and emergence of nuclear covalently closed circular DNA requires microtubules during entry only at and for specific time periods. Taken together, these data disclose for the first time a series of steps and their kinetics that are essential for the entry of hepatitis B viruses into hepatocytes and are different from those of any other virus reported so far. </jats:p> Itinerary of Hepatitis B Viruses: Delineation of Restriction Points Critical for Infectious Entry Journal of Virology
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title Itinerary of Hepatitis B Viruses: Delineation of Restriction Points Critical for Infectious Entry
title_unstemmed Itinerary of Hepatitis B Viruses: Delineation of Restriction Points Critical for Infectious Entry
title_full Itinerary of Hepatitis B Viruses: Delineation of Restriction Points Critical for Infectious Entry
title_fullStr Itinerary of Hepatitis B Viruses: Delineation of Restriction Points Critical for Infectious Entry
title_full_unstemmed Itinerary of Hepatitis B Viruses: Delineation of Restriction Points Critical for Infectious Entry
title_short Itinerary of Hepatitis B Viruses: Delineation of Restriction Points Critical for Infectious Entry
title_sort itinerary of hepatitis b viruses: delineation of restriction points critical for infectious entry
topic Virology
Insect Science
Immunology
Microbiology
url http://dx.doi.org/10.1128/jvi.78.15.8289-8300.2004
publishDate 2004
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description <jats:title>ABSTRACT</jats:title> <jats:p> Little is known about cellular determinants essential for human hepatitis B virus infection. Using the duck hepatitis B virus as a model, we first established a sensitive binding assay for both virions and subviral particles and subsequently elucidated the characteristics of the early viral entry steps. The infection itinerary was found to initiate with the attachment of viral particles to a low number of binding sites on hepatocytes (about 10 <jats:sup>4</jats:sup> per cell). Virus internalization was fully accomplished in less than 3 h but was then followed by a period of unprecedented length, about 14 h, until completion of nuclear import of the viral genome. Steps subsequent to virus entry depended on both intact microtubules and their dynamic turnover but not on actin cytoskeleton. Notably, cytoplasmic trafficking of viral particles and emergence of nuclear covalently closed circular DNA requires microtubules during entry only at and for specific time periods. Taken together, these data disclose for the first time a series of steps and their kinetics that are essential for the entry of hepatitis B viruses into hepatocytes and are different from those of any other virus reported so far. </jats:p>
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description <jats:title>ABSTRACT</jats:title> <jats:p> Little is known about cellular determinants essential for human hepatitis B virus infection. Using the duck hepatitis B virus as a model, we first established a sensitive binding assay for both virions and subviral particles and subsequently elucidated the characteristics of the early viral entry steps. The infection itinerary was found to initiate with the attachment of viral particles to a low number of binding sites on hepatocytes (about 10 <jats:sup>4</jats:sup> per cell). Virus internalization was fully accomplished in less than 3 h but was then followed by a period of unprecedented length, about 14 h, until completion of nuclear import of the viral genome. Steps subsequent to virus entry depended on both intact microtubules and their dynamic turnover but not on actin cytoskeleton. Notably, cytoplasmic trafficking of viral particles and emergence of nuclear covalently closed circular DNA requires microtubules during entry only at and for specific time periods. Taken together, these data disclose for the first time a series of steps and their kinetics that are essential for the entry of hepatitis B viruses into hepatocytes and are different from those of any other virus reported so far. </jats:p>
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spelling Funk, Anneke Mhamdi, Mouna Lin, Li Will, Hans Sirma, Hüseyin 0022-538X 1098-5514 American Society for Microbiology Virology Insect Science Immunology Microbiology http://dx.doi.org/10.1128/jvi.78.15.8289-8300.2004 <jats:title>ABSTRACT</jats:title> <jats:p> Little is known about cellular determinants essential for human hepatitis B virus infection. Using the duck hepatitis B virus as a model, we first established a sensitive binding assay for both virions and subviral particles and subsequently elucidated the characteristics of the early viral entry steps. The infection itinerary was found to initiate with the attachment of viral particles to a low number of binding sites on hepatocytes (about 10 <jats:sup>4</jats:sup> per cell). Virus internalization was fully accomplished in less than 3 h but was then followed by a period of unprecedented length, about 14 h, until completion of nuclear import of the viral genome. Steps subsequent to virus entry depended on both intact microtubules and their dynamic turnover but not on actin cytoskeleton. Notably, cytoplasmic trafficking of viral particles and emergence of nuclear covalently closed circular DNA requires microtubules during entry only at and for specific time periods. Taken together, these data disclose for the first time a series of steps and their kinetics that are essential for the entry of hepatitis B viruses into hepatocytes and are different from those of any other virus reported so far. </jats:p> Itinerary of Hepatitis B Viruses: Delineation of Restriction Points Critical for Infectious Entry Journal of Virology
spellingShingle Funk, Anneke, Mhamdi, Mouna, Lin, Li, Will, Hans, Sirma, Hüseyin, Journal of Virology, Itinerary of Hepatitis B Viruses: Delineation of Restriction Points Critical for Infectious Entry, Virology, Insect Science, Immunology, Microbiology
title Itinerary of Hepatitis B Viruses: Delineation of Restriction Points Critical for Infectious Entry
title_full Itinerary of Hepatitis B Viruses: Delineation of Restriction Points Critical for Infectious Entry
title_fullStr Itinerary of Hepatitis B Viruses: Delineation of Restriction Points Critical for Infectious Entry
title_full_unstemmed Itinerary of Hepatitis B Viruses: Delineation of Restriction Points Critical for Infectious Entry
title_short Itinerary of Hepatitis B Viruses: Delineation of Restriction Points Critical for Infectious Entry
title_sort itinerary of hepatitis b viruses: delineation of restriction points critical for infectious entry
title_unstemmed Itinerary of Hepatitis B Viruses: Delineation of Restriction Points Critical for Infectious Entry
topic Virology, Insect Science, Immunology, Microbiology
url http://dx.doi.org/10.1128/jvi.78.15.8289-8300.2004