New World hantaviruses activate IFNlambda production in type I IFN-deficient vero E6 cells.

Hantaviruses indigenous to the New World are the etiologic agents of hantavirus cardiopulmonary syndrome (HCPS). These viruses induce a strong interferon-stimulated gene (ISG) response in human endothelial cells. African green monkey-derived Vero E6 cells are used to propagate hantaviruses as well a...

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Main Authors: Joseph Prescott, Pamela Hall, Mariana Acuna-Retamar, Chunyan Ye, Marc G Wathelet, Hideki Ebihara, Heinz Feldmann, Brian Hjelle
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-06-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2887373?pdf=render
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author Joseph Prescott
Pamela Hall
Mariana Acuna-Retamar
Chunyan Ye
Marc G Wathelet
Hideki Ebihara
Heinz Feldmann
Brian Hjelle
author_facet Joseph Prescott
Pamela Hall
Mariana Acuna-Retamar
Chunyan Ye
Marc G Wathelet
Hideki Ebihara
Heinz Feldmann
Brian Hjelle
author_sort Joseph Prescott
collection DOAJ
description Hantaviruses indigenous to the New World are the etiologic agents of hantavirus cardiopulmonary syndrome (HCPS). These viruses induce a strong interferon-stimulated gene (ISG) response in human endothelial cells. African green monkey-derived Vero E6 cells are used to propagate hantaviruses as well as many other viruses. The utility of the Vero E6 cell line for virus production is thought to owe to their lack of genes encoding type I interferons (IFN), rendering them unable to mount an efficient innate immune response to virus infection. Interferon lambda, a more recently characterized type III IFN, is transcriptionally controlled much like the type I IFNs, and activates the innate immune system in a similar manner.We show that Vero E6 cells respond to hantavirus infection by secreting abundant IFNlambda. Three New World hantaviruses were similarly able to induce IFNlambda expression in this cell line. The IFNlambda contained within virus preparations generated with Vero E6 cells independently activates ISGs when used to infect several non-endothelial cell lines, whereas innate immune responses by endothelial cells are specifically due to viral infection. We show further that Sin Nombre virus replicates to high titer in human hepatoma cells (Huh7) without inducing ISGs.Herein we report that Vero E6 cells respond to viral infection with a highly active antiviral response, including secretion of abundant IFNlambda. This cytokine is biologically active, and when contained within viral preparations and presented to human epithelioid cell lines, results in the robust activation of innate immune responses. We also show that both Huh7 and A549 cell lines do not respond to hantavirus infection, confirming that the cytoplasmic RNA helicase pathways possessed by these cells are not involved in hantavirus recognition. We demonstrate that Vero E6 actively respond to virus infection and inhibiting IFNlambda production in these cells might increase their utility for virus propagation.
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spelling doaj.art-84b71633f0d24f0fa7f61b854d2b547b2022-12-21T17:50:44ZengPublic Library of Science (PLoS)PLoS ONE1932-62032010-06-0156e1115910.1371/journal.pone.0011159New World hantaviruses activate IFNlambda production in type I IFN-deficient vero E6 cells.Joseph PrescottPamela HallMariana Acuna-RetamarChunyan YeMarc G WatheletHideki EbiharaHeinz FeldmannBrian HjelleHantaviruses indigenous to the New World are the etiologic agents of hantavirus cardiopulmonary syndrome (HCPS). These viruses induce a strong interferon-stimulated gene (ISG) response in human endothelial cells. African green monkey-derived Vero E6 cells are used to propagate hantaviruses as well as many other viruses. The utility of the Vero E6 cell line for virus production is thought to owe to their lack of genes encoding type I interferons (IFN), rendering them unable to mount an efficient innate immune response to virus infection. Interferon lambda, a more recently characterized type III IFN, is transcriptionally controlled much like the type I IFNs, and activates the innate immune system in a similar manner.We show that Vero E6 cells respond to hantavirus infection by secreting abundant IFNlambda. Three New World hantaviruses were similarly able to induce IFNlambda expression in this cell line. The IFNlambda contained within virus preparations generated with Vero E6 cells independently activates ISGs when used to infect several non-endothelial cell lines, whereas innate immune responses by endothelial cells are specifically due to viral infection. We show further that Sin Nombre virus replicates to high titer in human hepatoma cells (Huh7) without inducing ISGs.Herein we report that Vero E6 cells respond to viral infection with a highly active antiviral response, including secretion of abundant IFNlambda. This cytokine is biologically active, and when contained within viral preparations and presented to human epithelioid cell lines, results in the robust activation of innate immune responses. We also show that both Huh7 and A549 cell lines do not respond to hantavirus infection, confirming that the cytoplasmic RNA helicase pathways possessed by these cells are not involved in hantavirus recognition. We demonstrate that Vero E6 actively respond to virus infection and inhibiting IFNlambda production in these cells might increase their utility for virus propagation.http://europepmc.org/articles/PMC2887373?pdf=render
spellingShingle Joseph Prescott
Pamela Hall
Mariana Acuna-Retamar
Chunyan Ye
Marc G Wathelet
Hideki Ebihara
Heinz Feldmann
Brian Hjelle
New World hantaviruses activate IFNlambda production in type I IFN-deficient vero E6 cells.
PLoS ONE
title New World hantaviruses activate IFNlambda production in type I IFN-deficient vero E6 cells.
title_full New World hantaviruses activate IFNlambda production in type I IFN-deficient vero E6 cells.
title_fullStr New World hantaviruses activate IFNlambda production in type I IFN-deficient vero E6 cells.
title_full_unstemmed New World hantaviruses activate IFNlambda production in type I IFN-deficient vero E6 cells.
title_short New World hantaviruses activate IFNlambda production in type I IFN-deficient vero E6 cells.
title_sort new world hantaviruses activate ifnlambda production in type i ifn deficient vero e6 cells
url http://europepmc.org/articles/PMC2887373?pdf=render
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