Comparison of replication-competent molecular clones of porcine endogenous retrovirus class A and class B derived from pig and human cells

被引:65
作者
Krach, U [1 ]
Fischer, N [1 ]
Czauderna, F [1 ]
Tönjes, RR [1 ]
机构
[1] Paul Ehrlich Inst, D-63225 Langen, Germany
关键词
D O I
10.1128/JVI.75.12.5465-5472.2001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Vertically transmitted endogenous retroviruses pose an infectious risk in the course of pig-to-human transplantation of cells, tissues, and organs. Two classes of polytropic type C porcine endogenous retroviruses (PERV) which are infectious for human cells in vitro are known. Recently, we described the cloning and characterization of replication-competent PERV-B sequences from productively infected human cells (F, Czauderna, N, Fischer, K, Boiler, R, Kurth, and R, R, Tonjes, J, Virol, 74:4028-4038, 2000). Here, we report the isolation of infectious molecular PERV-A and PERV-B clones from pig cells and compare these proviruses with clones derived from infected human 293 cells, In addition to clone PERV-A(42) derived from 293 cells, four "native" full-length proviral PERV sequences derived from a genomic library of the porcine cell line PK15 were isolated, Three identical class A clones, designated PK15-PERV-A(42), PK15-PERV-A(45), and PK15-PERV-A(58), and one class B clone, PK15-PERV-B(213), were characterized. PK15-PERV-B(213) is highly homologous but distinct from the previously described clone PERV-B(43). PK15-PERV-A(58) demonstrates close homology to PERV-A(42) in env and to PERV-C in long terminal repeat, gag, and pro/pol sequences. All three PERV clones described here were replication competent upon infection of susceptible cell lines. The findings suggest that the pig genome harbors a limited number of infectious PERV-A and -B sequences.
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页码:5465 / 5472
页数:8
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共 35 条
[11]  
Fishman Jay A., 1994, Xenotransplantation, V1, P47, DOI 10.1111/j.1399-3089.1994.tb00049.x
[13]   Generation and testing of a highly specific anti-serum directed against porcine endogenous retrovirus nucleocapsid [J].
Krach, U ;
Fischer, N ;
Czauderna, F ;
Kurth, R ;
Tönjes, RR .
XENOTRANSPLANTATION, 2000, 7 (03) :221-229
[14]   Two sets of human-tropic pig retrovirus [J].
LeTissier, P ;
Stoye, JP ;
Takeuchi, Y ;
Patience, C ;
Weiss, RA .
NATURE, 1997, 389 (6652) :681-682
[15]   Expression of pig endogenous retrovirus by primary porcine endothelial cells and infection of human cells [J].
Martin, U ;
Kiessig, V ;
Blusch, JH ;
Haverich, A ;
von der Helm, K ;
Herden, T ;
Steinhoff, G .
LANCET, 1998, 352 (9129) :692-694
[16]   Selection of reversions and suppressors of a mutation in the CBF binding site of a lymphomagenic retrovirus [J].
Martiney, MJ ;
Rulli, K ;
Beaty, R ;
Levy, LS ;
Lenz, J .
JOURNAL OF VIROLOGY, 1999, 73 (09) :7599-7606
[17]  
MERIC C, 1989, J VIROL, V63, P1558
[18]   XENOTRANSPLANT-ASSOCIATED ZOONOSES - STRATEGIES FOR PREVENTION [J].
MICHAELS, MG ;
SIMMONS, RL .
TRANSPLANTATION, 1994, 57 (01) :1-7
[19]   STRUCTURAL HOMOLOGY OF THE MAJOR INTERNAL PROTEINS OF ENDOGENOUS TYPE-C VIRUSES OF 2 DISTANTLY RELATED SPECIES OF OLD-WORLD MONKEYS - MACACA-ARCTOIDES AND COLOBUS-POLYKOMOS [J].
OROSZLAN, S ;
COPELAND, TD ;
GILDEN, RV ;
TODARO, GJ .
VIROLOGY, 1981, 115 (02) :262-271
[20]   Search for cross-species transmission of porcine endogenous retrovirus in patients treated with living pig tissue [J].
Paradis, K ;
Langford, G ;
Long, ZF ;
Heneine, W ;
Sandstrom, P ;
Switzer, WM ;
Chapman, LE ;
Lockey, C ;
Onions, D ;
Otto, E .
SCIENCE, 1999, 285 (5431) :1236-1241