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In Vitro and In Vivo Models for the Study of Human Polyomavirus Infection

Developments of genome amplification techniques have rapidly expanded the family of human polyomaviruses (PyV). Following infection early in life, PyV persist in their hosts and are generally of no clinical consequence. High-level replication of PyV can occur in patients under immunosuppressive or i...

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Autores principales: Barth, Heidi, Solis, Morgane, Kack-Kack, Wallys, Soulier, Eric, Velay, Aurélie, Fafi-Kremer, Samira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5086624/
https://www.ncbi.nlm.nih.gov/pubmed/27782080
http://dx.doi.org/10.3390/v8100292
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author Barth, Heidi
Solis, Morgane
Kack-Kack, Wallys
Soulier, Eric
Velay, Aurélie
Fafi-Kremer, Samira
author_facet Barth, Heidi
Solis, Morgane
Kack-Kack, Wallys
Soulier, Eric
Velay, Aurélie
Fafi-Kremer, Samira
author_sort Barth, Heidi
collection PubMed
description Developments of genome amplification techniques have rapidly expanded the family of human polyomaviruses (PyV). Following infection early in life, PyV persist in their hosts and are generally of no clinical consequence. High-level replication of PyV can occur in patients under immunosuppressive or immunomodulatory therapy and causes severe clinical entities, such as progressive multifocal leukoencephalopathy, polyomavirus-associated nephropathy or Merkel cell carcinoma. The characterization of known and newly-discovered human PyV, their relationship to human health, and the mechanisms underlying pathogenesis remain to be elucidated. Here, we summarize the most widely-used in vitro and in vivo models to study the PyV-host interaction, pathogenesis and anti-viral drug screening. We discuss the strengths and limitations of the different models and the lessons learned.
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spelling pubmed-50866242016-11-02 In Vitro and In Vivo Models for the Study of Human Polyomavirus Infection Barth, Heidi Solis, Morgane Kack-Kack, Wallys Soulier, Eric Velay, Aurélie Fafi-Kremer, Samira Viruses Review Developments of genome amplification techniques have rapidly expanded the family of human polyomaviruses (PyV). Following infection early in life, PyV persist in their hosts and are generally of no clinical consequence. High-level replication of PyV can occur in patients under immunosuppressive or immunomodulatory therapy and causes severe clinical entities, such as progressive multifocal leukoencephalopathy, polyomavirus-associated nephropathy or Merkel cell carcinoma. The characterization of known and newly-discovered human PyV, their relationship to human health, and the mechanisms underlying pathogenesis remain to be elucidated. Here, we summarize the most widely-used in vitro and in vivo models to study the PyV-host interaction, pathogenesis and anti-viral drug screening. We discuss the strengths and limitations of the different models and the lessons learned. MDPI 2016-10-22 /pmc/articles/PMC5086624/ /pubmed/27782080 http://dx.doi.org/10.3390/v8100292 Text en © 2016 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 Review
Barth, Heidi
Solis, Morgane
Kack-Kack, Wallys
Soulier, Eric
Velay, Aurélie
Fafi-Kremer, Samira
In Vitro and In Vivo Models for the Study of Human Polyomavirus Infection
title In Vitro and In Vivo Models for the Study of Human Polyomavirus Infection
title_full In Vitro and In Vivo Models for the Study of Human Polyomavirus Infection
title_fullStr In Vitro and In Vivo Models for the Study of Human Polyomavirus Infection
title_full_unstemmed In Vitro and In Vivo Models for the Study of Human Polyomavirus Infection
title_short In Vitro and In Vivo Models for the Study of Human Polyomavirus Infection
title_sort in vitro and in vivo models for the study of human polyomavirus infection
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5086624/
https://www.ncbi.nlm.nih.gov/pubmed/27782080
http://dx.doi.org/10.3390/v8100292
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