Publication:
Sendai virus, a strong inducer of anti-lentiviral state in ovine cells

Consultable a partir de

Date

2020

Authors

Rius-Rocabert, Sergio
Luján, Lluís
Garcin, Dominique
Nistal Villán, Estanislao

Director

Publisher

MDPI
Acceso abierto / Sarbide irekia
Artículo / Artikulua
Versión publicada / Argitaratu den bertsioa

Project identifier

AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/RTI2018-096172-B-C31/ES/
Gobierno de Navarra//

Abstract

Small ruminant lentiviruses (SRLVs) are widely spread in the ovine and caprine populations, causing an incurable disease aecting animal health and production. Vaccine development is hindered owing to the high genetic heterogeneity of lentiviruses and the selection of T-cell and antibody escape mutants, requiring antigen delivery optimization. Sendai virus (SeV) is a respiratory paramyxovirus in mice that has been recognized as a potent inducer of innate immune responses in several species, including mouse and human. The aim of this study was to stimulate an innate antiviral response in ovine cells and evaluate the potential inhibitory eect upon small ruminant lentivirus (SRLV) infections. Ovine alveolar macrophages (AMs), blood-derived macrophages (BDMs), and skin fibroblasts (OSFs) were stimulated through infection with SeV encoding green fluorescent protein (GFP). SeV eciently infected ovine cells, inducing an antiviral state in AM from SRLV naturally-infected animals, as well as in in vitro SRLV-infected BDM and OSF from non-infected animals. Supernatants from SeV-infected AM induced an antiviral state when transferred to fresh cells challenged with SRLV. Similar to SRLV, infectivity of an HIV-1-GFP lentiviral vector was also restricted in ovine cells infected with SeV. In myeloid cells, an M1-like proinflammatory polarization was observed together with an APOBEC3Z1 induction, among other lentiviral restriction factors. Our observations may boost new approximations in ameliorating the SRLV burden by stimulation of the innate immune response using SeV-based vaccine vectors.

Keywords

Small ruminant lentivirus, Sendai virus, Innate immunity, Interferon, APOBEC3

Department

Agronomía, Biotecnología y Alimentación / Agronomia, Bioteknologia eta Elikadura

Faculty/School

Degree

Doctorate program

Editor version

Funding entities

This research was funded by Spanish Ministry of Science, Innovation, and Universities, grant number RTI2018-096172-B-C31; Consejo Superior de Investigaciones Científicas, i-Coop and EMHE Program; and by Government of Navarra (CONECTIM) and by Project NIETO-CM B2017/BMD-3731 to E.N.-V. The APC was funded by the CSIC Open Access Publication Support Initiative through its Unit of Information Resources for Research (URICI).

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