Enterotropic mouse hepatitis virus

被引:57
作者
Homberger, FR
机构
[1] Institute of Laboratory Animal Science, University of Zurich
[2] Institute of Laboratory Animal Science, University of Zurich, 8057 Zurich
关键词
coronavirus; mouse hepatitis virus; enterotropic; mouse;
D O I
10.1258/002367797780600189
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Mouse hepatitis virus (MHV), the coronavirus of the mouse, is the most common viral pathogen in contemporary laboratory mouse colonies throughout the world. It is highly contagious with variable clinical manifestations. The majority of infections are subclinical, but can still significantly influence biological responses, thus interfering with research, mainly in the field of immunology. MHV has been intensively studied from a number of research perspectives and has become the prototype for studying the molecular biology of coronaviruses. MHV contains a single-stranded, positive-sense RNA genome ranging from 27 to 31 kb, which is divided into seven genes. Virions consist of four to five structural proteins. There are many MHV strains that vary in virulence, organotropism and cell tropism, and are constantly evolving by naturally occurring mutation and recombination. Based on pathogenesis studies MHV strains are usually grouped according to their primary tissue tropism into two biotypes: polytropic and enterotropic. Enterotropic strains of MHV replicate in the intestinal mucosa and only rarely spread to other tissues. No morphological structure of the virion has as yet been identified that is responsible for enterotropism. The course of an MHV infection is dependent on the virus strain and host factors. Generally, MHV causes an acute, self-limiting infection which is inapparent in adult mice. Neonates are highly susceptible to disease and show high mortality. In an enzootically infected colony, however, they are protected by maternally derived passive immunity. Detection of MHV infections depends on serological screening of colonies. MHV is controlled by culling and rederivation of the affected colony using hysterectomy or embryo transfer or by elimination through cessation of breeding.
引用
收藏
页码:97 / 115
页数:19
相关论文
共 141 条
[81]  
LAI MMC, 1994, INFECT AGENT DIS, V3, P98
[82]   CORONAVIRUS - ORGANIZATION, REPLICATION AND EXPRESSION OF GENOME [J].
LAI, MMC .
ANNUAL REVIEW OF MICROBIOLOGY, 1990, 44 :303-333
[83]   RNA RECOMBINATION IN ANIMAL AND PLANT-VIRUSES [J].
LAI, MMC .
MICROBIOLOGICAL REVIEWS, 1992, 56 (01) :61-79
[84]   CELL-FREE TRANSLATION OF MURINE CORONAVIRUS RNA [J].
LEIBOWITZ, JL ;
WEISS, SR ;
PAAVOLA, E ;
BOND, CW .
JOURNAL OF VIROLOGY, 1982, 43 (03) :905-913
[85]   INDUCTION OF MONOCYTE PROCOAGULANT ACTIVITY BY MURINE HEPATITIS-VIRUS TYPE-3 PARALLELS DISEASE SUSCEPTIBILITY IN MICE [J].
LEVY, GA ;
LEIBOWITZ, JL ;
EDGINGTON, TS .
JOURNAL OF EXPERIMENTAL MEDICINE, 1981, 154 (04) :1150-1163
[86]  
Lindsey J. R., 1986, Viral and mycoplasmal infections of laboratory rodents. Effects on biomedical research., P801
[87]   EVALUATION OF ISOLATOR CAGING SYSTEMS FOR PROTECTION OF MICE AGAINST CHALLENGE WITH MOUSE HEPATITIS-VIRUS [J].
LIPMAN, NS ;
CORNING, BF ;
SAIFUDDIN, M .
LABORATORY ANIMALS, 1993, 27 (02) :134-140
[88]   THE PATTERN OF PROTEINS SYNTHESIZED IN THE LIVER IS PROFOUNDLY MODIFIED UPON INFECTION OF SUSCEPTIBLE MICE WITH MOUSE HEPATITIS VIRUS-3 [J].
LUCCHIARI, MA ;
PEREIRA, CA ;
KUHN, L ;
LEFKOVITS, I .
RESEARCH IN VIROLOGY, 1992, 143 (04) :231-240
[89]  
MANAKER RA, 1961, JNCI-J NATL CANCER I, V27, P29
[90]   IMMUNE-RESPONSE TO A MURINE CORONAVIRUS - IDENTIFICATION OF A HOMING RECEPTOR-NEGATIVE CD4+ T-CELL SUBSET THAT RESPONDS TO VIRAL GLYCOPROTEINS [J].
MOBLEY, J ;
EVANS, G ;
DAILEY, MO ;
PERLMAN, S .
VIROLOGY, 1992, 187 (02) :443-452