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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Methods in cell science 11 (1988), S. 113-121 
    ISSN: 1573-0603
    Keywords: exotic species ; monolayer cultures ; avian tracheal ring organ cultures ; viral sensitivity ; serum studies ; viral diagnoses
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Methods for the preparation, cultivation, preservation, and maintenance of serially passaged cell cultures derived from different tissues of exotic or threatened animals and certain species of birds are described. The diagnoses of viral pathogens affecting exotic and domestic species were enhanced by the availability of such cell or avian tracheal ring organ cultures to the veterinary diagnostic virology laboratory. Cell cultures from exotic species derived from tissues of bighorn sheep, white-tailed gnu, white-tailed deer, oryx, aoudad sheep, cockatiels, and ring-necked pheasants were developed or obtained by our laboratory. These cell cultures were examined for cellular morphology and growth characteristics at two different temperatures, presence of adventitious agents, and karyotype. Several of the exotic cell lines supported the replication of various viruses associated with avian and mammalian hosts. As comparison, cell cultures of domestic sheep were used. Tracheal ring organ cultures from chickens, turkeys, and pheasants were also assayed for their sensitivity to selected viruses. Cell cultures from exotic species may provide a viable alternative for the detection of viruses from such species which heretofore have been difficult to isolate using cell lines derived from domestic species.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-0603
    Keywords: alcelaphine herpesviruses ; malignant catarrhal fever ; cell culture ; electron microscopy ; virus isolation ; serologic methods
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Cultures of fetal aoudad sheep kidney (FAK), bovine embryonic lung (BEL), and African green monkey kidney (Vero) cells were compared for differential replication of alcelaphine herpesviruses. Cell-free virus appears more rapidly when infected cells are incubated at 33° C rather than at 37° C. Events in the replication and morphologic development of several alcelaphine herpesvirus isolates have been documented using light and electron microscopy. Techniques for indirect immunofluorescence and serum virus neutralization are described. When virus free of host-cell contaminants is desired for biochemical analysis, virus isolates are initially purified on sucrose gradients and then further purified by density gradient centrifugation in Percoll.
    Type of Medium: Electronic Resource
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