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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Online Access: | https://doi.org/10.1371/journal.pone.0123087 |
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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 |
work_keys_str_mv |
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