Key result
Human astroviruses induce a mild and delayed type I interferon response in CaCo-2 cells that occurs at late stages of infection after genome replication has taken place.
Human astroviruses induce a delayed type I interferon response in intestinal cells, allowing viral replication to occur before the host antiviral defense is fully activated.
May permit astrovirus evasion of early gut immunity; leaves open its contribution to human gastroenteritis pathogenesis.
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.
No takes yet. Share an insight, caveat, or question.
Guix et al. (2015) studied Human Astrovirus Infection. Human Astrovirus (HAstV) infection vs. Mock-infected cells was evaluated on Type I Interferon (IFN-β) mRNA expression and antiviral activity. Human astroviruses induce a mild and delayed type I interferon response in CaCo-2 cells that occurs at late stages of infection after genome replication has taken place.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: