Selective receptor expression restricts Nipah virus infection of endothelial cells

<p>Abstract</p> <p>Nipah virus (NiV) is a highly pathogenic paramyxovirus that causes severe diseases in animals and humans. Endothelial cell (EC) infection is an established hallmark of NiV infection <it>in vivo</it>. Despite systemic virus spread via the vascular syst...

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Main Authors: Diederich Sandra, Erbar Stephanie, Maisner Andrea
Format: Article
Language:English
Published: BMC 2008-11-01
Series:Virology Journal
Online Access:http://www.virologyj.com/content/5/1/142
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spelling doaj-607bae64fb7f4106bf2673f299f309a92020-11-25T00:25:26ZengBMCVirology Journal1743-422X2008-11-015114210.1186/1743-422X-5-142Selective receptor expression restricts Nipah virus infection of endothelial cellsDiederich SandraErbar StephanieMaisner Andrea<p>Abstract</p> <p>Nipah virus (NiV) is a highly pathogenic paramyxovirus that causes severe diseases in animals and humans. Endothelial cell (EC) infection is an established hallmark of NiV infection <it>in vivo</it>. Despite systemic virus spread via the vascular system, EC in brain and lung are preferentially infected whereas EC in other organs are less affected. As <it>in vivo</it>, we found differences in the infection of EC in cell culture. Only brain-derived primary or immortalized EC were found to be permissive to NiV infection. Using a replication-independent fusion assay, we could show that the lack of infection in non-brain EC was due to a lack of receptor expression. The NiV entry receptors ephrinB2 (EB2) or ephrinB3 were only expressed in brain endothelia. The finding that EB2 expression in previously non-permissive aortic EC rendered the cells permissive to infection then demonstrated that EB2 is not only necessary but also sufficient to allow the establishment of a productive NiV infection. This strongly suggests that limitations in receptor expression restrict virus entry in certain EC subsets <it>in vivo</it>, and are thus responsible for the differences in EC tropism observed in human and animal NiV infections.</p> http://www.virologyj.com/content/5/1/142
collection DOAJ
language English
format Article
sources DOAJ
author Diederich Sandra
Erbar Stephanie
Maisner Andrea
spellingShingle Diederich Sandra
Erbar Stephanie
Maisner Andrea
Selective receptor expression restricts Nipah virus infection of endothelial cells
Virology Journal
author_facet Diederich Sandra
Erbar Stephanie
Maisner Andrea
author_sort Diederich Sandra
title Selective receptor expression restricts Nipah virus infection of endothelial cells
title_short Selective receptor expression restricts Nipah virus infection of endothelial cells
title_full Selective receptor expression restricts Nipah virus infection of endothelial cells
title_fullStr Selective receptor expression restricts Nipah virus infection of endothelial cells
title_full_unstemmed Selective receptor expression restricts Nipah virus infection of endothelial cells
title_sort selective receptor expression restricts nipah virus infection of endothelial cells
publisher BMC
series Virology Journal
issn 1743-422X
publishDate 2008-11-01
description <p>Abstract</p> <p>Nipah virus (NiV) is a highly pathogenic paramyxovirus that causes severe diseases in animals and humans. Endothelial cell (EC) infection is an established hallmark of NiV infection <it>in vivo</it>. Despite systemic virus spread via the vascular system, EC in brain and lung are preferentially infected whereas EC in other organs are less affected. As <it>in vivo</it>, we found differences in the infection of EC in cell culture. Only brain-derived primary or immortalized EC were found to be permissive to NiV infection. Using a replication-independent fusion assay, we could show that the lack of infection in non-brain EC was due to a lack of receptor expression. The NiV entry receptors ephrinB2 (EB2) or ephrinB3 were only expressed in brain endothelia. The finding that EB2 expression in previously non-permissive aortic EC rendered the cells permissive to infection then demonstrated that EB2 is not only necessary but also sufficient to allow the establishment of a productive NiV infection. This strongly suggests that limitations in receptor expression restrict virus entry in certain EC subsets <it>in vivo</it>, and are thus responsible for the differences in EC tropism observed in human and animal NiV infections.</p>
url http://www.virologyj.com/content/5/1/142
work_keys_str_mv AT diederichsandra selectivereceptorexpressionrestrictsnipahvirusinfectionofendothelialcells
AT erbarstephanie selectivereceptorexpressionrestrictsnipahvirusinfectionofendothelialcells
AT maisnerandrea selectivereceptorexpressionrestrictsnipahvirusinfectionofendothelialcells
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