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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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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