Journal of Virology, March 2001, p. 2771-2775, Vol. 75, No. 6
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.6.2771-2775.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Institute of Cancer Research,1 University College London,4 and National Institute for Medical Research,5 London, United Kingdom; Bio Transplant Incorporated, Charlestown, Massachusetts2; and HIV and Retrovirology Branch, Centers for Disease Control and Prevention, Atlanta, Georgia3
Received 5 September 2000/Accepted 20 December 2000
In view of the concern over potential infection hazards in the use
of porcine tissues and organs for xenotransplantation to humans, we investigated the diversity of porcine endogenous retrovirus (PERV) genomes in the DNA of domestic pigs and related species. In
addition to the three known envelope subgroups of infectious gamma
retroviruses (PERV-A, -B, and -C), classed together here as PERV group
1, four novel groups of gamma retrovirus (
2 to
5) and four
novel groups of beta retrovirus (
1 to
4) genomes were detected in
pig DNA using generic and specific PCR primers. PCR quantification
indicated that the retroviral genome copy number in the Landrace × Duroc F1 hybrid pig ranged from 2 (
2 and
5) to
approximately 50 (
1). The
1,
2, and
4 genomes were
transcribed into RNA in adult kidney tissue. Apart from
1, the
retroviral genomes are not known to be infectious, and sequencing of a
small number of amplified genome fragments revealed stop codons in
putative open reading frames in several cases. Analysis of DNA from
wild boar and other species of Old World pigs (Suidae) and
New World peccaries (Tayassuidae) showed that one
retrovirus group,
2, was common to all species tested, while the
others were present among all Old World species but absent from New
World species. The PERV-C subgroup of
1 genomes segregated among
domestic pigs and were absent from two African species (red river hog
and warthog). Thus domestic swine and their phylogenetic relatives
harbor multiple groups of hitherto undescribed PERV genomes.
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