The effects of gamma interferon on replication of foot-and-mouth disease virus in persistently infected bovine cells

被引:72
作者
Zhang, ZD [1 ]
Hutching, G [1 ]
Kitching, P [1 ]
Alexandersen, S [1 ]
机构
[1] Inst Anim Hlth, Pirbright Lab, Pirbright, England
关键词
D O I
10.1007/s00705-002-0867-6
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Foot-and-mouth disease virus (FMDV) causes a highly contagious viral disease of cloven-hoofed animals, which has a considerable socio-economic impact on the countries affected. In addition, persistent infection can occur following clinical or sub-clinical disease in either vaccinated or non-vaccinated cattle. The mechanism(s) by which FMDV persistence is established and maintained is not fully understood. To better understand the basic mechanisms controlling the virus infection in cattle, the effects of interferon gamma (IFN-gamma) on the replication of FMDV was evaluated in vitro in persistently infected-epithelial cells isolated from FMDV infected cattle. Initially primary bovine thyroid (BTY) cells were treated with varying doses of bovine recombinant IFN-gamma. The cytokine activity was measured by detection of viral antigen in cell supernatants and viral RNA expression compared with cells without INF-gamma treatment. Pretreatment with IFN-gamma profoundly affected FMDV growth in BTY cells. The replication of FMDV was affected in the presence of more than 2.5 u/ml of IFN-gamma and the effect was both dose-dependent and related to the time of exposure. Analysis of the mechanism of inhibition suggests that IFN-gamma did not inhibit the viral replication through induction of nitric oxide. More interesting is the finding that continuous treatment with IFN-gamma severely restricts FMDV replication or even cures persistently infected bovine epithelial cells, indicating that a cytokine-mediated pathway may be involved in the in vivo clearance of persistent FMDV.
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页码:2157 / 2167
页数:11
相关论文
共 22 条
[1]   The early pathogenesis of foot-and-mouth disease in pigs infected by contact: a quantitative time-course study using TaqMan RT-PCR [J].
Alexandersen, S ;
Oleksiewicz, MB ;
Donaldson, AI .
JOURNAL OF GENERAL VIROLOGY, 2001, 82 :747-755
[2]  
ALEXANDERSEN S, 2002, IN PRESS MICRO INFEC
[3]   FOOT-AND-MOUTH DISEASE [J].
BACHRACH, HL .
ANNUAL REVIEW OF MICROBIOLOGY, 1968, 22 :201-+
[4]   Interferon gamma and interleukin 1, but not interferon alfa, inhibit rotavirus entry into human intestinal cell lines [J].
Bass, DM .
GASTROENTEROLOGY, 1997, 113 (01) :81-89
[5]   IFNγ inhibits porcine reproductive and respiratory syndrome virus replication in macrophages [J].
Bautista, EM ;
Molitor, TW .
ARCHIVES OF VIROLOGY, 1999, 144 (06) :1191-1200
[6]   Demonstration of bovine CD8+ T-cell responses to foot and mouth disease virus [J].
Childerstone, AJ ;
Cedillo-Baron, L ;
Foster-Cuevas, M ;
Parkhouse, RME .
JOURNAL OF GENERAL VIROLOGY, 1999, 80 :663-669
[7]   Ability of foot-and-mouth disease virus to form plaques in cell culture is associated with suppression of alpha/beta interferon [J].
Chinsangaram, J ;
Piccone, ME ;
Grubman, MJ .
JOURNAL OF VIROLOGY, 1999, 73 (12) :9891-9898
[8]   Interferon-gamma inhibits HIV-induced invasiveness of monocytes [J].
Dhawan, S ;
Wahl, LM ;
Heredia, A ;
Zhang, YH ;
Epstein, JS ;
Meltzer, MS ;
Hewlett, IK .
JOURNAL OF LEUKOCYTE BIOLOGY, 1995, 58 (06) :713-716
[9]   Modulation of dengue virus infection in human cells by alpha, beta, and gamma interferons [J].
Diamond, MS ;
Roberts, TG ;
Edgil, D ;
Lu, B ;
Ernst, J ;
Harris, E .
JOURNAL OF VIROLOGY, 2000, 74 (11) :4957-4966
[10]   ULTRASTRUCTURAL AND REPLICATIVE FEATURES OF FOOT-AND-MOUTH-DISEASE VIRUS IN PERSISTENTLY INFECTED BHK-21-CELLS [J].
DONN, A ;
CASTAGNARO, M ;
DONALDSON, AI .
ARCHIVES OF VIROLOGY, 1995, 140 (01) :13-25