Immunofluorescence and cytochemical studies of visna virus in cell culture.

Characterization of a membrane-associated protein implicated in visna virus binding and infection.

The identity of the cellular receptor(s) for visna virus, an ovine lentivirus, is currently unknown; however, previous studies from our laboratory have identified membrane-associated proteins expressed selectively in susceptible cells which bind visna virus. Moreover, a polyclonal antibody (2-23), raised against a 45-kDa visna virus binding protein, bound specifically to the surface of suscepti...

Cytochemical studies with African Horse-Sickness Virus by Fluorescent Microscopy

Cytochemical and immunofluorescence study of an oncogenic avian adenovirus (CELO) in mammalian cell cultures.

Chicken embryo lethal orphan (CELO) virus replication studies in adult hamster kidney and green monkey kidney cell cultures by means of infectivity, cytochemistry, and fluorescent-antibody techniques indicated that replication in hamster kidney cells was limited to the production of neoantigen. Production of virus in green monkey kidney cells was limited but appeared to exceed the production of...

Preparation of a cell line persistently infected with maedi/visna virus and production of viral antigens

We attempted to prepare a cell line that produces maedi/visna virus (MVV) and is free of contamination by other viruses and mycoplasmas. Three cell lines, which originated from a sheep, goat and bat, were infected with MVV and passaged approximately every 5 days. The cultured cells were then subjected to polymerase chain reaction analysis for MVV provirus. As a result, a cell line persistently ...

The long terminal repeat is a determinant of cell tropism of maedi-visna virus.

Maedi-visna virus (MVV) is a lentivirus of sheep, mainly affecting the lungs and the central nervous system. Long terminal repeat (LTR) sequence variability is common in tissue culture-derived isolates of MVV as well as those of other lentiviruses. The role of this sequence variation in MVV replication has not been explored. PCR amplification of the LTRs of an MVV isolate revealed two product s...