Type I interferon response is delayed in human astrovirus infections.

Type I interferon (IFN) activation and its subsequent effects are important in the response to viral infections. Here we show that human astroviruses (HAstVs), which are important agents of acute gastroenteritis in children, induce a mild and delayed IFN response upon infecting CaCo-2 cells. Althoug...

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Main Authors: Susana Guix, Anna Pérez-Bosque, Lluïsa Miró, Miquel Moretó, Albert Bosch, Rosa M Pintó
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0123087
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spelling doaj-b85d0a739e59412da916def45f57b6502021-03-03T20:06:49ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01104e012308710.1371/journal.pone.0123087Type I interferon response is delayed in human astrovirus infections.Susana GuixAnna Pérez-BosqueLluïsa MiróMiquel MoretóAlbert BoschRosa M PintóType I interferon (IFN) activation and its subsequent effects are important in the response to viral infections. Here we show that human astroviruses (HAstVs), which are important agents of acute gastroenteritis in children, induce a mild and delayed IFN response upon infecting CaCo-2 cells. Although IFN-β mRNA is detected within infected cells and supernatant from infected cells show antiviral activity against the replication of other well-known IFN-sensitive viruses, these responses occur at late stages of infection once genome replication has taken place. On the other hand, HAstV replication can be partially reduced by the addition of exogenous IFN, and inhibition of IFN activation by BX795 enhances viral replication, indicating that HAstVs are IFN-sensitive viruses. Finally, different levels of IFN response were observed in cells infected with different HAstV mutants with changes in the hypervariable region of nsP1a/4, suggesting that nsP1a/4 genotype may potentially have clinical implications due to its correlation with the viral replication phenotype and the antiviral responses induced within infected cells.https://doi.org/10.1371/journal.pone.0123087
collection DOAJ
language English
format Article
sources DOAJ
author Susana Guix
Anna Pérez-Bosque
Lluïsa Miró
Miquel Moretó
Albert Bosch
Rosa M Pintó
spellingShingle Susana Guix
Anna Pérez-Bosque
Lluïsa Miró
Miquel Moretó
Albert Bosch
Rosa M Pintó
Type I interferon response is delayed in human astrovirus infections.
PLoS ONE
author_facet Susana Guix
Anna Pérez-Bosque
Lluïsa Miró
Miquel Moretó
Albert Bosch
Rosa M Pintó
author_sort Susana Guix
title Type I interferon response is delayed in human astrovirus infections.
title_short Type I interferon response is delayed in human astrovirus infections.
title_full Type I interferon response is delayed in human astrovirus infections.
title_fullStr Type I interferon response is delayed in human astrovirus infections.
title_full_unstemmed Type I interferon response is delayed in human astrovirus infections.
title_sort type i interferon response is delayed in human astrovirus infections.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description Type I interferon (IFN) activation and its subsequent effects are important in the response to viral infections. Here we show that human astroviruses (HAstVs), which are important agents of acute gastroenteritis in children, induce a mild and delayed IFN response upon infecting CaCo-2 cells. Although IFN-β mRNA is detected within infected cells and supernatant from infected cells show antiviral activity against the replication of other well-known IFN-sensitive viruses, these responses occur at late stages of infection once genome replication has taken place. On the other hand, HAstV replication can be partially reduced by the addition of exogenous IFN, and inhibition of IFN activation by BX795 enhances viral replication, indicating that HAstVs are IFN-sensitive viruses. Finally, different levels of IFN response were observed in cells infected with different HAstV mutants with changes in the hypervariable region of nsP1a/4, suggesting that nsP1a/4 genotype may potentially have clinical implications due to its correlation with the viral replication phenotype and the antiviral responses induced within infected cells.
url https://doi.org/10.1371/journal.pone.0123087
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