| Literature DB >> 26280469 |
Giulia Cacciotti1, Beniamino Caputo2, Carla Selvaggi1, Andrea la Sala3, Laura Vitiello3, Diawo Diallo4, Cornelia Ceianu5, Guido Antonelli1, Norbert Nowotny6, Carolina Scagnolari7.
Abstract
Given the pivotal role of monocyte-derived dendritic cells (DCs) in determining the magnitude of the antiviral innate immune response, we sought to determine whether Usutu virus (USUV) and West Nile virus (WNV) lineages (L)1 and L2 can infect DCs and affect the rate of type I interferon (IFN) activation. The sensitivity of these viruses to types I and III IFNs was also compared. We found that USUV can infect DCs, induce higher antiviral activities, IFN alpha subtypes and the IFN stimulated gene (ISG)15 pathway, and is more sensitive to types I and III IFNs than WNVs. In contrast, we confirmed that IFN alpha/beta subtypes were more effective against WNV L2 than WNV L1. However, the replication kinetics, induction of IFN alpha subtypes and ISGs in DCs and the sensitivity to IFN lambda 1-3 did not differ between WNV L1 and L2.Entities:
Keywords: IFN; Interferon; Monocyte-derived dendritic cells; USUV; Usutu virus; WNV; West Nile virus
Mesh:
Substances:
Year: 2015 PMID: 26280469 DOI: 10.1016/j.virol.2015.07.015
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616