SJL/J mice are highly susceptible to infection by mouse adenovirus type I

被引:36
作者
Spindler, KR
Fang, L
Moore, ML
Hirsch, GN
Brown, CC
Kajon, A
机构
[1] Univ Georgia, Dept Genet, Franklin Coll Arts & Sci, Athens, GA 30602 USA
[2] Univ Georgia, Coll Vet Med, Dept Vet Pathol, Athens, GA 30602 USA
关键词
D O I
10.1128/JVI.75.24.12039-12046.2001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Mouse adenovirus type 1 (MAV-1) targets endothelial and monocyte/macrophage cells throughout the mouse. Depending on the strain of mouse and dose or strain of virus, infected mice may survive, become persistently infected, or die. We surveyed inbred mouse strains and found that for the majority tested the 50% lethal doses (LD(50)s) were > 10(4.4) PFU. However, SJL/J mice were highly susceptible to MAV-1, with a mean LD50 of 10(-0.32) PFU. Infected C3H/HeJ (resistant) and SJL/J (susceptible) mice showed only modest differences in histopathology. Susceptible mice had significantly higher viral loads in the brain and spleen at 8 days postinfection than resistant mice. Infection of primary macrophages or mouse embryo fibroblasts from SJL/J and C3H/HeJ mice gave equivalent yields of virus, suggesting that a receptor difference between strains is not responsible for the susceptibility difference. When C3H/HeJ mice were subjected to sublethal doses of gamma irradiation, they became susceptible to MAV-1, with an LD50 like that of SJL/J mice. Antiviral immunoglobulin G (IgG) levels were measured in susceptible and resistant mice infected by an early region IA null mutant virus that is less virulent that wild-type virus. The antiviral IgG levels were high and similar in the two strains of mice. Taken together, these results suggest that immune response differences may in part account for differences in susceptibility to MAV-1 infection.
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收藏
页码:12039 / 12046
页数:8
相关论文
共 48 条
[1]   EARLY REGION-4 SEQUENCE AND BIOLOGICAL COMPARISON OF 2 ISOLATES OF MOUSE ADENOVIRUS TYPE-1 [J].
BALL, AO ;
BEARD, CW ;
VILLEGAS, P ;
SPINDLER, KR .
VIROLOGY, 1991, 180 (01) :257-265
[2]   Analysis of early region 3 mutants of mouse adenovirus type 1 [J].
Beard, CW ;
Spindler, KR .
JOURNAL OF VIROLOGY, 1996, 70 (09) :5867-5874
[3]  
Bedell MA, 1996, GENETICS, V142, P927
[4]   MURINE T-CELL RECEPTOR MUTANTS WITH DELETIONS OF BETA-CHAIN VARIABLE REGION GENES [J].
BEHLKE, MA ;
CHOU, HS ;
HUPPI, K ;
LOH, DY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (03) :767-771
[5]   PRE-EARLY ADENOVIRUS-5 GENE-PRODUCT REGULATES SYNTHESIS OF EARLY VIRAL MESSENGER-RNAS [J].
BERK, AJ ;
LEE, F ;
HARRISON, T ;
WILLIAMS, J ;
SHARP, PA .
CELL, 1979, 17 (04) :935-944
[6]   Positional cloning of the mouse retrovirus restriction gene Fv1 [J].
Best, S ;
LeTissier, P ;
Towers, G ;
Stoye, JP .
NATURE, 1996, 382 (6594) :826-829
[7]   GENETIC-RESISTANCE TO MOUSE HEPATITIS-VIRUS CORRELATES WITH ABSENCE OF VIRUS-BINDING ACTIVITY ON TARGET TISSUES [J].
BOYLE, JF ;
WEISMILLER, DG ;
HOLMES, KV .
JOURNAL OF VIROLOGY, 1987, 61 (01) :185-189
[8]  
BRETT S, 1992, IMMUNOLOGY, V76, P129
[9]   In vitro and in vivo characterization of a mouse adenovirus type 1 early region 3 null mutant [J].
Cauthen, AN ;
Brown, CC ;
Spindler, KR .
JOURNAL OF VIROLOGY, 1999, 73 (10) :8640-8646
[10]  
CAUTHEN AN, 1999, METH MOLEC MED, V21, P85