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Study of the virulence of serotypes 4 and 9 of African horse sickness virus in IFNAR-/-, Balb/C and 129 Sv/Ev mice
被引:3
作者:
de la Grandiere, Maria Ana
[1
]
Dal Pozzo, Fabiana
[2
]
Tignon, Marylene
[3
]
Zonta, William
[1
]
Thiry, Damien
[1
]
Mauroy, Axel
[1
]
Mathijs, Elisabeth
[4
]
Caij, Ann Brigitte
[2
,3
]
Saegerman, Claude
Thiry, Etienne
[1
]
机构:
[1] Univ Liege, Fac Vet Med, FARAH, B-4000 Liege, Belgium
[2] Univ Liege, Fac Vet Med, Res Unit Epidemiol & Risk Anal Appl Vet Sci UREA, B-4000 Liege, Belgium
[3] Operat Direct Viral Dis Vet & Agrochem Res Ctr, Unit Enzoot & Re Emerging Viral Dis, Brussels, Belgium
[4] Vet & Agrochem Res Ctr, Virol Platform Unit, Operat Direct Viral Dis, Brussels, Belgium
关键词:
African horse sickness virus;
Orbivirus;
Mice;
Virulence;
PLASMACYTOID DENDRITIC CELLS;
I INTERFERON;
BLUETONGUE;
TIME;
RESPONSES;
INFECTION;
SYSTEM;
LETHAL;
ASSAY;
RNA;
D O I:
10.1016/j.vetmic.2014.10.006
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
African horse sickness virus (AHSV) is a double-stranded RNA virus which belongs to the family Reoviridae, genus Orbivinis. Recent studies have focused on the interferon-alp 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. (C) 2014 Elsevier B.V. All Tights reserved.
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页码:322 / 332
页数:11
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