Host range and interference studies of three classes of pig endogenous retrovirus

被引:355
作者
Takeuchi, Y
Patience, C
Magre, S
Weiss, RA
Banerjee, PT
Le Tissier, P
Stoye, JP
机构
[1] Inst Canc Res, Chester Beatty Labs, London SW3 6JB, England
[2] Biotransplant Inc, Charlestown, MA USA
[3] Natl Inst Med Res, London NW7 1AA, England
基金
英国医学研究理事会;
关键词
D O I
10.1128/JVI.72.12.9986-9991.1998
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Recent interest in the use of porcine organs, tissues, and cells for xenotransplantation to humans has highlighted the need to characterize the properties of pig endogenous retroviruses (PERVs). Analysis of a variety of pig cells allowed us to isolate and identify three classes of infectious type C endogenous retrovirus (PERV-A, PERV-B, and PERV-C) which have distinct env genes but have highly homologous sequences in the rest of the genome. To study the properties of these env genes, expression plasmids for the three env genes were constructed and used to generate retrovirus vectors bearing corresponding Env proteins. Host range analyses by the vector transduction assay showed that PERV-A and PERV-B Envs have wider host ranges, including several human cell lines, compared with PERV-C Env, which infected only two pig cell lines and one human cell line. All PERVs could infect pig cells, indicating that the PERVs have a potential to replicate in pig transplants in immunosuppressed patients. Receptors for PERV-A and PERV-B were present on cells of some other species, including mink, rat, mouse, and dog, suggesting that such species may provide useful model systems to study infection and pathogenicity of PERV. In contrast, no vector transduction was observed on nonhuman primate cell lines, casting doubt on the utility of nonhuman primates as models for PERV zoonosis. Interference studies showed that the three PERV strains use receptors distinct from each other and from a number of other type C mammalian retroviruses.
引用
收藏
页码:9986 / 9991
页数:6
相关论文
共 40 条
[1]  
*ADV GROUP ETH XEN, 1997, AN TISS HUM
[2]   Identification of a full-length cDNA for an endogenous retrovirus of miniature swine [J].
Akiyoshi, DE ;
Denaro, M ;
Zhu, HH ;
Greenstein, JL ;
Banerjee, P ;
Fishman, JA .
JOURNAL OF VIROLOGY, 1998, 72 (05) :4503-4507
[3]   Xenotransplantation at a crossroads: Prevention versus progress [J].
Allan, JS .
NATURE MEDICINE, 1996, 2 (01) :18-21
[4]   RECEPTOR-BINDING DOMAIN OF MURINE LEUKEMIA-VIRUS ENVELOPE GLYCOPROTEINS [J].
BATTINI, JL ;
DANOS, O ;
HEARD, JM .
JOURNAL OF VIROLOGY, 1995, 69 (02) :713-719
[5]   RECEPTOR CHOICE DETERMINANTS IN THE ENVELOPE GLYCOPROTEINS OF AMPHOTROPIC, XENOTROPIC, AND POLYTROPIC MURINE LEUKEMIA VIRUSES [J].
BATTINI, JL ;
HEARD, JM ;
DANOS, O .
JOURNAL OF VIROLOGY, 1992, 66 (03) :1468-1475
[6]  
Butler D, 1998, NATURE, V391, P320
[7]   HIGH-TITER PACKAGING CELLS PRODUCING RECOMBINANT RETROVIRUSES RESISTANT TO HUMAN SERUM [J].
COSSET, FL ;
TAKEUCHI, Y ;
BATTINI, JL ;
WEISS, RA ;
COLLINS, MKL .
JOURNAL OF VIROLOGY, 1995, 69 (12) :7430-7436
[8]   RETROVIRAL RETARGETING BY ENVELOPES EXPRESSING AN N-TERMINAL BINDING DOMAIN [J].
COSSET, FL ;
MORLING, FJ ;
TAKEUCHI, Y ;
WEISS, RA ;
COLLINS, MKL ;
RUSSELL, SJ .
JOURNAL OF VIROLOGY, 1995, 69 (10) :6314-6322
[9]   Histological evidence of fetal pig neural cell survival after transplantation into a patient with Parkinson's disease [J].
Deacon, T ;
Schumacher, J ;
Dinsmore, J ;
Thomas, C ;
Palmer, P ;
Kott, S ;
Edge, A ;
Penney, D ;
Kassissieh, S ;
Dempsey, P ;
Isacson, O .
NATURE MEDICINE, 1997, 3 (03) :350-353
[10]  
Fishman Jay A., 1994, Xenotransplantation, V1, P47, DOI 10.1111/j.1399-3089.1994.tb00049.x