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  • 1
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In 8 of 10 wild rats trapped in The Netherlands, an infectious viruslike agent was isolated predominantly from the salivary glands and could be serially passed in laboratory rats. In rat embryo cells a typical cytomegalo-like cytopathic effect was produced. The morphologic and cultural characteristics of the isolated agent were comparable with those of the mouse cytomegalovirus (MCMV). The virus-nucleocapsid had a size of 92 nm and was not ether-resistant. The extracellular nucleocapsids were often enclosed by an outer layer of very variable shape and size. The formation of Fc receptors on cells infected with the rat virus could be demonstrated. The wild rats possessed neutralizing antibodies to the isolated agent. The rat agent grew only in rat embryo fibroblast cells while MCMV grew in rat and mouse embryo cells. The rat agent gave plaques in REF monolayers. Electron microscope studies showed the presence of nucleocapsids in the nucleus.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Archives of virology 76 (1983), S. 189-199 
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary This report described the infection of two strains of laboratory rats with a rativirus (RA-1) with cytomegalovirus-like characteristics. The virus was detected in the spleens and kidneys during the first week post infection. In the salivary glands maximal virus titer was reached at one month post infection; thereafter the titer declined. In Lewis rats virus could be detected in the salivary homogenate of most animals at more than 12 months post infection. In BN rats, in contrast, virus became undetectable in the salivary glands of most animals 5 months after inoculation. However, adminstration of cyclophosphamide or X-irradiation resulted in reactivation of the virus in virtually all animals. Co-cultivation of spleen cells from either latently or chronically infected animals resulted in recovery of virus. The animals developed antibodies and a T-cell mediated virus specific cytotoxicity.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Infection of rat embryonic fibroblasts (REF) and R2 cells with rat cytomegalovirus (RCMV) resulted in the formation of cytoplasmic and membrane receptors for the Fc region of immunoglobulin G. The Fc receptors were demonstrated by the immunocytochemical techniques using indirect fluorescence and peroxidase technique at the light microscope level and using the protein A adsorbed to colloidal gold technique for demonstration at the electron microscope level. The production level of demonstration at the electron microscope level. The production level of the Fc receptor in the cell was depending on the input of virus. Experiments with ara C, cycloheximide and actinomycin D revealed that the formation of the Fc receptor was dependent on RNA, DNA and protein synthesis. Furthermore, results indicate that redistribution of the Fc receptor to form a cap, takes place within the first 60 minutes.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In this paper the development of a battery of approximately 70 mouse monoclonal antibodies (McAbs) to RCMV-induced antigens and their characterization is discussed. Their reactivity with the whole scala of ca. 30 virus specific proteins was tested in an enzyme linked immunoassay (ELISA) whereas their ability to detect RCMV-antigens at different locations ofin vitro infected cell cultures and at different stages of infection was tested by immunofluorescence. In order to determine to what specific (viral) protein each of these McAbs is directed against we used an immunoprecipitation technique, followed by SDS-PAGE. Furthermore, neutralizing capacity of each McAb was tested, as well as the immunoglobulin class they belong to. In this manner we defined six categories of monoclonal antibodies on the basis of immunofluorescence aspect. The six categories identify most important viral structural proteins.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Rat cytomegalovirus (RCMV) induces a cytosol thymidine kinase (TK) in G0-phase rat embryo fibroblasts (REF), but not in a TK deficient rat cell line (R-2), though virus titers in both cell types reached comparable levels. The results indicate that TK is neither virus-coded nor is required for a productive infection in R-2 cells. A deoxycytidine kinase (dCK) is induced in either growing or RCMV-infected REF and R-2 cells, suggesting that dCK is essential for both host-cell and viral DNA synthesis. A deoxy-guanosine kinase (dGK) is detectable in low concentrations in either growing or G0-phase REF and R-2 cells suggesting that this enzyme is cell-cycle independent. In contrast, RCMV induces high persisting levels of dGK, particularly in R-2 cells, indicating that this enzyme is of crucial importance for viral DNA synthesis. By comparison of thermostabilities and electrophoretic mobilities (Rf for TK, dCK and dGK were 0.12; 0.97; and 0.54, respectively) the enzymes were found to be substrate specific but of cellular origin. In contrast to TK and dCK, only dGK is inhibited by Acyclovir (Ki=320 µm). It is suggested that RCMV inducable dGK is an important enzyme determining thein vitro anti-CMV activity of Acyclovir.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-1440
    Keywords: Allograft arteriosclerosis ; Chronic allograft rejection ; Growth factors ; Smooth muscle cell replication
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Chronic allograft rejection is the major reason why allografts are lost. While only 2%-3% of all allografts are lost during the first year to irreversible acute rejection, approximately 6%–7% are lost during each subsequent year to chronic rejection. The major manifestation of chronic rejection in all organs is persistent perivascular inflammation and allograft arteriosclerosis. Bearing this in mind, we have developed a model to investigate the pathophysiology of allograft arteriosclerosis using aortic transplantations between inbred rat strains. The results obtained thus far indicate that several different inflammatory cascades are operative within the vascular wall during allograft arteriosclerosis. The relative importance of these different cascades, and particularly the role of growth factors as final effectors, has not yet been defined. Attempts to suppress allograft arteriosclerosis under experimental conditions have already met with some success: under conditions where no immunosuppression is provided we have been able to delay the process by at least 3 months, though we have not been able to block it indefinitely. It may be expected, however, that once the inflammatory cascades leading to smooth muscle cell replication in the allograft media and their influx into the intima are better defined, more specific approaches to the inhibition of allograft arteriosclerosis will be developed.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Archives of virology 42 (1973), S. 371-377 
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Reovirus immune serum prepared by intravenous immunization of rabbits with the concentrated L cell culture fluid does not only contain virus-neutralizing and haemagglutination-inhibiting antibodies, but also complement fixing antibodies and precipitins against both reovirus antigens and cellular antigens. Active immunization by application of concentrated reovirus-containing cell culture fluid on the scarified skin results in the development of comparable antibody levels against reovirus, whereas demonstrable antibody to cellular antigens fails to develop. Hence, the complement fixation and immunoprecipitation tests are reovirus-specific. In contrast to the fairly typespecific neutralizing and haemagglutination-inhibiting antibodies, the complement fixing antibodies and the precipitins are group-specific.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Archives of virology 82 (1984), S. 247-247 
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Archives of virology 97 (1987), S. 27-35 
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Subcutaneous (s.c.) administration of Acyclovir (ACV) (100 mg/1 kg bodyweight) resulted in an ACV blood level of 80 µM at 2 h post infection. Thereafter the level declined rapidly reaching undetectable levels at 12 h post infection. Administration of pro-ACV (100 mg/kg body weight) by s.c. or intravenous (i.v.) route resulted in ACV levels of 75 µM and 160 µM respectively after 30 min. But here again the blood level of ACV declined rapidly and was completely disappeared after 12 h. Continuous administration of pro-ACV in daily doses of 100, 250 and 350 mg/kg body weight resulted in ACV blood levels of 15 µM, 19 µM and 39 µM, respectively. The effect of ACV and pro-ACV on the replication of CMV was measured in immunesuppressed rats. In rats inoculated with RCMV the daily administration of 25 to 50 mg ACV per kg body weight by s.c. injections twice daily, did not result in a reduction of virus titers in spleen and liver, but when the RCMV-infected rats were treated by 100 mg pro-ACV per kg body weight virus titers in the spleen and liver were significantly reduced as compared with those in sham-treated animals.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Archives of virology 42 (1973), S. 378-387 
    ISSN: 1432-8798
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary A reovirus containing cell culture fluid may be segregated in three reovirusantigen containing fractions. Fractionation is achieved by chromatography on Ecteola-cellulose and by centrifugation in a sucrose density gradient. Virions could be separated from non-infective reovirus particles by centrifugation in a sucrose density gradient. The non-infective reovirus-antigens could further be separated into haemagglutinating particles and into particles giving a complement-fixation and a precipitation line with immune serum by chromatography on Ecteola-cellulose.
    Type of Medium: Electronic Resource
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