Shedding light on the elusive role of endothelial cells in cytomegalovirus dissemination.

Cytomegalovirus (CMV) is frequently transmitted by solid organ transplantation and is associated with graft failure. By forming the boundary between circulation and organ parenchyma, endothelial cells (EC) are suited for bidirectional virus spread from and to the transplant. We applied Cre/loxP-medi...

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Main Authors: Torsten Sacher, Joachim Andrassy, Aivars Kalnins, Lars Dölken, Stefan Jordan, Jürgen Podlech, Zsolt Ruzsics, Karl-Walter Jauch, Matthias J Reddehase, Ulrich H Koszinowski
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-11-01
Series:PLoS Pathogens
Online Access:http://europepmc.org/articles/PMC3219709?pdf=render
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spelling doaj-faf192d4110440b4bc75a3af3fa0a0db2020-11-25T01:08:22ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742011-11-01711e100236610.1371/journal.ppat.1002366Shedding light on the elusive role of endothelial cells in cytomegalovirus dissemination.Torsten SacherJoachim AndrassyAivars KalninsLars DölkenStefan JordanJürgen PodlechZsolt RuzsicsKarl-Walter JauchMatthias J ReddehaseUlrich H KoszinowskiCytomegalovirus (CMV) is frequently transmitted by solid organ transplantation and is associated with graft failure. By forming the boundary between circulation and organ parenchyma, endothelial cells (EC) are suited for bidirectional virus spread from and to the transplant. We applied Cre/loxP-mediated green-fluorescence-tagging of EC-derived murine CMV (MCMV) to quantify the role of infected EC in transplantation-associated CMV dissemination in the mouse model. Both EC- and non-EC-derived virus originating from infected Tie2-cre(+) heart and kidney transplants were readily transmitted to MCMV-naïve recipients by primary viremia. In contrast, when a Tie2-cre(+) transplant was infected by primary viremia in an infected recipient, the recombined EC-derived virus poorly spread to recipient tissues. Similarly, in reverse direction, EC-derived virus from infected Tie2-cre(+) recipient tissues poorly spread to the transplant. These data contradict any privileged role of EC in CMV dissemination and challenge an indiscriminate applicability of the primary and secondary viremia concept of virus dissemination.http://europepmc.org/articles/PMC3219709?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Torsten Sacher
Joachim Andrassy
Aivars Kalnins
Lars Dölken
Stefan Jordan
Jürgen Podlech
Zsolt Ruzsics
Karl-Walter Jauch
Matthias J Reddehase
Ulrich H Koszinowski
spellingShingle Torsten Sacher
Joachim Andrassy
Aivars Kalnins
Lars Dölken
Stefan Jordan
Jürgen Podlech
Zsolt Ruzsics
Karl-Walter Jauch
Matthias J Reddehase
Ulrich H Koszinowski
Shedding light on the elusive role of endothelial cells in cytomegalovirus dissemination.
PLoS Pathogens
author_facet Torsten Sacher
Joachim Andrassy
Aivars Kalnins
Lars Dölken
Stefan Jordan
Jürgen Podlech
Zsolt Ruzsics
Karl-Walter Jauch
Matthias J Reddehase
Ulrich H Koszinowski
author_sort Torsten Sacher
title Shedding light on the elusive role of endothelial cells in cytomegalovirus dissemination.
title_short Shedding light on the elusive role of endothelial cells in cytomegalovirus dissemination.
title_full Shedding light on the elusive role of endothelial cells in cytomegalovirus dissemination.
title_fullStr Shedding light on the elusive role of endothelial cells in cytomegalovirus dissemination.
title_full_unstemmed Shedding light on the elusive role of endothelial cells in cytomegalovirus dissemination.
title_sort shedding light on the elusive role of endothelial cells in cytomegalovirus dissemination.
publisher Public Library of Science (PLoS)
series PLoS Pathogens
issn 1553-7366
1553-7374
publishDate 2011-11-01
description Cytomegalovirus (CMV) is frequently transmitted by solid organ transplantation and is associated with graft failure. By forming the boundary between circulation and organ parenchyma, endothelial cells (EC) are suited for bidirectional virus spread from and to the transplant. We applied Cre/loxP-mediated green-fluorescence-tagging of EC-derived murine CMV (MCMV) to quantify the role of infected EC in transplantation-associated CMV dissemination in the mouse model. Both EC- and non-EC-derived virus originating from infected Tie2-cre(+) heart and kidney transplants were readily transmitted to MCMV-naïve recipients by primary viremia. In contrast, when a Tie2-cre(+) transplant was infected by primary viremia in an infected recipient, the recombined EC-derived virus poorly spread to recipient tissues. Similarly, in reverse direction, EC-derived virus from infected Tie2-cre(+) recipient tissues poorly spread to the transplant. These data contradict any privileged role of EC in CMV dissemination and challenge an indiscriminate applicability of the primary and secondary viremia concept of virus dissemination.
url http://europepmc.org/articles/PMC3219709?pdf=render
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