In-vivo Activity of IFN-λ and IFN-α Against Bovine-Viral-Diarrhea Virus in a Mouse Model
Author(s) -
María Eugenia Quintana,
Lucas José Barone,
Myrian Vanesa Trotta,
Cecilia Soledad Turco,
Florencia Celeste Mansilla,
Alejandra Victoria Capozzo,
Nancy Cardoso
Publication year - 2020
Publication title -
frontiers in veterinary science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.877
H-Index - 31
ISSN - 2297-1769
DOI - 10.3389/fvets.2020.00045
Subject(s) - viremia , in vivo , virulence , virology , infectivity , biology , virus , potency , vaccination , immunity , in vitro , immunology , microbiology and biotechnology , immune system , gene , biochemistry
Bovine-viral-diarrhea virus (BVDV) can cause significant economic losses in livestock. The disease is controlled with vaccination and bovines are susceptible until vaccine immunity develops and may remain vulnerable if a persistently infected animal is left on the farm; therefore, an antiviral agent that reduces virus infectivity can be a useful tool in control programs. Although many compounds with promising in-vitro efficacy have been identified, the lack of laboratory-animal models limited their potential for further clinical development. Recently, we described the activity of type I and III interferons, IFN-α and IFN-λ respectively, against several BVDV strains in-vitro . In this study, we analyzed the in-vivo efficacy of both IFNs using a BALB/c-mouse model. Mice infected with two type-2 BVDV field strains developed a viremia with different kinetics, depending on the infecting strain's virulence, that persisted for 56 days post-infection (dpi). Mice infected with the low-virulence strain elicited high systemic TNF-α levels at 2 dpi. IFNs were first applied subcutaneously 1 day before or after infection. The two IFNs reduced viremia with different kinetics, depending on whether either one was applied before or after infection. In a second experiment, we increased the number of applications of both IFNs. All the treatments reduced viremia compared to untreated mice. The application of IFN-λ pre- and post-infection reduced viremia over time. This study is the first proof of the concept of the antiviral potency of IFN-λ against BVDV in-vivo , thus encouraging further trails for a potential use of this cytokine in cattle.
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