The histopathology and ultrastructure of S V2O-induced intraperitoneal ( I P ) neoplasms is described and compared to neoplasms induced by this virus administered bySeveral simian adenoviruses are oncogenic for the hamster (Hull et al., 1965; Rapoza et al., 1967;Slifkin et al., 1968; Merkow et al., 1968a, b). The ability of simian adenovirus 20 (SV20) to initiate neoplasms capable of metastasizing appears to vary according to the route of inoculation. Intraperitoneal inoculation (IP) results in widespread multifocal abdominal neoplasms as well as distant metastases, whereas subcutaneous (Rapoza et al., 1967) and intracranial (Merkow et al., 19686) inoculations result in only localized tumors which infiltrate contiguous structures.This communication is a description of the histopathology, ultrastructure and biological activity of SV20-induced IP neoplasms and their comparison to SV20 neoplasms induced by other routes.
MATERIAL AND METHODSThe Chin (A57) strain of SV20 virus was used throughout this investigation. Its origin has been previously described (Hoffert et al., 1958). Virus stocks used in these investigations were prepared in the LLC-MK2 line (American Type Culture Collection, Rockville, Md., USA) of African green monkey kidney cells, in a medium containing SV5 and SV40 antisera. These stocks were free of SV40 virus and adeno-associated viruses, when tested by previously described procedures (Rapoza et al., 1967). Virus stocks were purified by centrifuging specimens, after freezing and thawing, in the Spinco model L ultra-centrifuge. Preparative density gradient centrifugation was used as a further step in purification (Slifkin et