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Polar release of pathogenic Old World hantaviruses from renal tubular epithelial cells

BACKGROUND: Epithelio- and endotheliotropic viruses often exert polarized entry and release that may be responsible for viral spread and dissemination. Hantaviruses, mostly rodent-borne members of the Bunyaviridae family infect epithelial and endothelial cells of different organs leading to organ dy...

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Autores principales: Krautkrämer, Ellen, Lehmann, Maik J, Bollinger, Vanessa, Zeier, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3546954/
https://www.ncbi.nlm.nih.gov/pubmed/23194647
http://dx.doi.org/10.1186/1743-422X-9-299
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author Krautkrämer, Ellen
Lehmann, Maik J
Bollinger, Vanessa
Zeier, Martin
author_facet Krautkrämer, Ellen
Lehmann, Maik J
Bollinger, Vanessa
Zeier, Martin
author_sort Krautkrämer, Ellen
collection PubMed
description BACKGROUND: Epithelio- and endotheliotropic viruses often exert polarized entry and release that may be responsible for viral spread and dissemination. Hantaviruses, mostly rodent-borne members of the Bunyaviridae family infect epithelial and endothelial cells of different organs leading to organ dysfunction or even failure. Endothelial and renal epithelial cells belong to the target cells of Old World hantavirus. Therefore, we examined the release of hantaviruses in several renal epithelial cell culture models. We used Vero cells that are commonly used in hantavirus studies and primary human renal epithelial cells (HREpC). In addition, we analyzed MDCKII cells, an epithelial cell line of a dog kidney, which represents a widely accepted in vitro model of polarized monolayers for their permissiveness for hantavirus infection. RESULTS: Vero C1008 and primary HREpCs were grown on porous-support filter inserts for polarization. Monolayers were infected with hantavirus Hantaan (HTNV) and Puumala (PUUV) virus. Supernatants from the apical and basolateral chamber of infected cells were analyzed for the presence of infectious particles by re-infection of Vero cells. Viral antigen and infectious particles of HTNV and PUUV were exclusively detected in supernatants collected from the apical chamber of infected Vero C1008 cells and HREpCs. MDCKII cells were permissive for hantavirus infection and polarized MDCKII cells released infectious hantaviral particles from the apical surface corresponding to the results of Vero and primary human epithelial cells. CONCLUSIONS: Pathogenic Old World hantaviruses are released from the apical surface of different polarized renal epithelial cells. We characterized MDCKII cells as a suitable polarized cell culture model for hantavirus infection studies.
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spelling pubmed-35469542013-01-17 Polar release of pathogenic Old World hantaviruses from renal tubular epithelial cells Krautkrämer, Ellen Lehmann, Maik J Bollinger, Vanessa Zeier, Martin Virol J Research BACKGROUND: Epithelio- and endotheliotropic viruses often exert polarized entry and release that may be responsible for viral spread and dissemination. Hantaviruses, mostly rodent-borne members of the Bunyaviridae family infect epithelial and endothelial cells of different organs leading to organ dysfunction or even failure. Endothelial and renal epithelial cells belong to the target cells of Old World hantavirus. Therefore, we examined the release of hantaviruses in several renal epithelial cell culture models. We used Vero cells that are commonly used in hantavirus studies and primary human renal epithelial cells (HREpC). In addition, we analyzed MDCKII cells, an epithelial cell line of a dog kidney, which represents a widely accepted in vitro model of polarized monolayers for their permissiveness for hantavirus infection. RESULTS: Vero C1008 and primary HREpCs were grown on porous-support filter inserts for polarization. Monolayers were infected with hantavirus Hantaan (HTNV) and Puumala (PUUV) virus. Supernatants from the apical and basolateral chamber of infected cells were analyzed for the presence of infectious particles by re-infection of Vero cells. Viral antigen and infectious particles of HTNV and PUUV were exclusively detected in supernatants collected from the apical chamber of infected Vero C1008 cells and HREpCs. MDCKII cells were permissive for hantavirus infection and polarized MDCKII cells released infectious hantaviral particles from the apical surface corresponding to the results of Vero and primary human epithelial cells. CONCLUSIONS: Pathogenic Old World hantaviruses are released from the apical surface of different polarized renal epithelial cells. We characterized MDCKII cells as a suitable polarized cell culture model for hantavirus infection studies. BioMed Central 2012-11-30 /pmc/articles/PMC3546954/ /pubmed/23194647 http://dx.doi.org/10.1186/1743-422X-9-299 Text en Copyright ©2012 Krautkrämer et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Krautkrämer, Ellen
Lehmann, Maik J
Bollinger, Vanessa
Zeier, Martin
Polar release of pathogenic Old World hantaviruses from renal tubular epithelial cells
title Polar release of pathogenic Old World hantaviruses from renal tubular epithelial cells
title_full Polar release of pathogenic Old World hantaviruses from renal tubular epithelial cells
title_fullStr Polar release of pathogenic Old World hantaviruses from renal tubular epithelial cells
title_full_unstemmed Polar release of pathogenic Old World hantaviruses from renal tubular epithelial cells
title_short Polar release of pathogenic Old World hantaviruses from renal tubular epithelial cells
title_sort polar release of pathogenic old world hantaviruses from renal tubular epithelial cells
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3546954/
https://www.ncbi.nlm.nih.gov/pubmed/23194647
http://dx.doi.org/10.1186/1743-422X-9-299
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