Study of the virulence of serotypes 4 and 9 of African horse sickness virus in IFNAR(-/-), Balb/C and 129 Sv/Ev mice.

Vet Microbiol

Veterinary Virology and Animal Viral Diseases, Fundamental and Applied Research on Animal and Health (FARAH), Faculty of Veterinary Medicine, University of Liège, B-4000 Liège, Belgium. Electronic address:

Published: December 2014

African horse sickness virus (AHSV) is a double-stranded RNA virus which belongs to the family Reoviridae, genus Orbivirus. Recent studies have focused on the interferon-α/β receptor knock-out mice (IFNAR(-/-)) as a small animal laboratory for the development of AHSV vaccines. The aim of this work was to study in vivo the virulence of two strains of AHSV and to compare the outcome of the infection of three mouse strains. To address this, AHSV serotypes 4 (AHSV-4) and 9 (AHSV-9) were inoculated subcutaneously (SC) and intranasally (IN) in two immunocompetent mouse strains (Balb/C and 129 Sv/Ev (129 WT)) as well as IFNAR(-/-) mice (on 129 Sv/Ev genetic background). In IFNAR(-/-) mice, fatality up to 50% was measured and significantly more clinical signs were observed in comparison with SC inoculated immunocompetent mice. The observed clinical signs were significantly more severe after AHSV-4 infection, in particular in immunocompetent mice inoculated by IN route. Considering RNAemia, significantly higher viral loads were measured following AHSV-4 infection. In the organs of 129 WT inoculated by IN route, significantly higher viral loads were detected after AHSV-4 infection. Together the results support a higher virulence for AHSV-4 compared to AHSV-9 and a higher clinical impact following infections in IN inoculated mice, at least in the investigated strains. The study also brought indirect evidences for type I IFN involvement in the control of AHSV infection.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.vetmic.2014.10.006DOI Listing

Publication Analysis

Top Keywords

129 sv/ev
12
ahsv-4 infection
12
african horse
8
horse sickness
8
sickness virus
8
balb/c 129
8
mouse strains
8
ifnar-/- mice
8
clinical signs
8
immunocompetent mice
8

Similar Publications

Chronic social defeat stress gives rise to social avoidance through fear learning.

Behav Brain Res

January 2025

Department of Psychology, Hunter College, City University of New York, New York, NY, USA; Psychology Program, The Graduate Center, City University of New York, New York, NY, USA. Electronic address:

Article Synopsis
  • - The study explores how chronic social defeat stress (CSDS) affects social behavior in vulnerable mice, particularly focusing on the male 129 Sv/Ev strain, which shows decreased social interactions and avoidance of a specific type of mouse (CD-1) as a threat response.
  • - Researchers find that defeated 129 Sv/Ev mice learn to associate the CD-1 mouse's appearance with feelings of threat over time, suggesting that their social avoidance is a learned fear response rather than complete social withdrawal.
  • - The findings also indicate that the avoidance behavior can be diminished through social interactions over several days, and individual differences exist in how these mice respond to social targets, highlighting the complexity of fear conditioning in social contexts. *
View Article and Find Full Text PDF

Infections with persistent or latent viruses alter host immune homeostasis and have potential to affect the outcome of concomitant acute viral infections such as influenza A virus (IAV). Gammaherpesviruses establish life-long infections and require an on-going immune response to control reactivation. We have used a murine model of co-infection to investigate the response to IAV infection in mice latently infected with the gammaherpesvirus MHV-68.

View Article and Find Full Text PDF

Bone metabolism and repair are directly regulated by arachidonic acid metabolites. At present, we analyzed the dose-response effects of a selective cysteinyl leukotriene receptor type-1 antagonist during bone repair after tooth extraction and on non-injured skeleton. Sixty-three 129 Sv/Ev male mice composed the groups: C-Control (saline solution); MTK2-2 mg/Kg of Montelukast (MTK) and MTK4-4 mg/Kg of MTK, daily administered by mouth throughout all experimental periods set at 7, 14, and 21 days post-operative.

View Article and Find Full Text PDF

Background: While improvements in immunoradiotherapy have significantly improved outcomes for cancer patients, this treatment approach has nevertheless proven ineffective at controlling the majority of malignancies. One of the mechanisms of resistance to immunoradiotherapy is that immune cells may be suppressed via the myriad of different immune checkpoint receptors. Therefore, simultaneous blockade of multiple immune checkpoint receptors may enhance the treatment efficacy of immunoradiotherapy.

View Article and Find Full Text PDF

Lysinuric protein intolerance (LPI) is an inborn error of cationic amino acid (arginine, lysine, ornithine) transport caused by biallelic pathogenic variants in SLC7A7, which encodes the light subunit of the y+LAT1 transporter. Treatments for the complications of LPI, including growth failure, renal disease, pulmonary alveolar proteinosis, autoimmune disorders and osteoporosis, are limited. Given the early lethality of the only published global Slc7a7 knockout mouse model, a viable animal model to investigate global SLC7A7 deficiency is needed.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!