Identification of receptors for pig endogenous retrovirus.

TitleIdentification of receptors for pig endogenous retrovirus.
Publication TypeJournal Article
Year of Publication2003
AuthorsEricsson TA, Takeuchi Y, Templin C, Quinn G, Farhadian SF, Wood JC, Oldmixon BA, Suling KM, Ishii JK, Kitagawa Y, Miyazawa T, Salomon DR, Weiss RA, Patience C
JournalProc Natl Acad Sci U S A
Volume100
Issue11
Pagination6759-64
Date Published2003 May 27
ISSN0027-8424
KeywordsAmino Acid Sequence, Animals, Base Sequence, DNA Primers, Endogenous Retroviruses, HeLa Cells, Humans, Mice, Molecular Sequence Data, Receptors, Virus, Sequence Homology, Amino Acid, Swine
Abstract

Xenotransplantation of porcine tissues has the potential to treat a wide variety of major health problems including organ failure and diabetes. Balanced against the potential benefits of xenotransplantation, however, is the risk of human infection with a porcine microorganism. In particular, the transmission of porcine endogenous retrovirus (PERV) is a major concern [Chapman, L. E. & Bloom, E. T. (2001) J. Am. Med. Assoc. 285, 2304-2306]. Here we report the identification of two, sequence-related, human proteins that act as receptors for PERV-A, encoded by genes located on chromosomes 8 and 17. We also describe homologs from baboon and porcine cells that also are active as receptors. Conversely, activity could not be demonstrated with a syntenic murine receptor homolog. Sequence analysis indicates that PERV-A receptors [human PERV-A receptor (HuPAR)-1, HuPAR-2, baboon PERV-A receptor 2, and porcine PERV-A receptor] are multiple membrane-spanning proteins similar to receptors for other gammaretroviruses. Expression is widespread in human tissues including peripheral blood mononuclear cells, but their biological functions are unknown. The identification of the PERV-A receptors opens avenues of research necessary for a more complete assessment of the retroviral risks of pig to human xenotransplantation.

DOI10.1073/pnas.1138025100
Alternate JournalProc. Natl. Acad. Sci. U.S.A.
PubMed ID12740431
PubMed Central IDPMC164520
Grant ListR01 AI045494 / AI / NIAID NIH HHS / United States
R01 AI45494 / AI / NIAID NIH HHS / United States

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