Identification of a full-length cDNA for an endogenous retrovirus of miniature swine

DE Akiyoshi, M Denaro, H Zhu, JL Greenstein… - Journal of …, 1998 - Am Soc Microbiol
DE Akiyoshi, M Denaro, H Zhu, JL Greenstein, P Banerjee, JA Fishman
Journal of virology, 1998Am Soc Microbiol
Endogenous retroviruses of swine are a concern in the use of pig-derived tissues for
xenotransplantation into humans. The nucleotide sequence of porcine endogenous
retrovirus taken from lymphocytes of miniature swine (PERV-MSL) has been characterized.
PERV-MSL is a type C retrovirus of 8,132 bp with the greatest nucleic acid sequence identity
to gibbon ape leukemia virus and murine leukemia virus. Constitutive production of PERV-
MSL RNA has been detected in normal leukocytes and in multiple organs of swine. The …
Abstract
Endogenous retroviruses of swine are a concern in the use of pig-derived tissues for xenotransplantation into humans. The nucleotide sequence of porcine endogenous retrovirus taken from lymphocytes of miniature swine (PERV-MSL) has been characterized. PERV-MSL is a type C retrovirus of 8,132 bp with the greatest nucleic acid sequence identity to gibbon ape leukemia virus and murine leukemia virus. Constitutive production of PERV-MSL RNA has been detected in normal leukocytes and in multiple organs of swine. The copy numbers of full-length PERV sequences per genome (approximately 8 to 15) vary among swine strains. The open reading frames for gag, pol, andenv in PERV-MSL have over 99% amino acid sequence identity to those of Tsukuba-1 retrovirus and are highly homologous to those of endogenous retrovirus of cell line PK15 (PK15-ERV). Most of the differences in the predicted amino acid sequences of PK15-ERV and PERV-MSL are in the SU (cell attach- ment) region ofenv. The existence of these PERV clones will enable studies of infection by endogenous retroviruses in xenotransplantation.
American Society for Microbiology