Mapping Full-Length Porcine Endogenous Retroviruses in a Large White Pig

ABSTRACT Xenotransplantation may bridge the widening gap between the shortage of donor organs and the increasing number of patients waiting for transplantation. However, a major safety issue is the potential cross-species transmission of porcine endogenous retroviruses (PERV). This problem could be resolved if it is possible to produce pigs that do not contain replication-competent copies of this virus. In order to determine the feasibility of this, we have determined the number of potentially replication-competent full-length PERV proviruses and obtained data on their integration sites within the porcine genome. We have screened genomic DNA libraries from a Large White pig for potentially intact proviruses. We identified six unique PERV B proviruses that were apparently intact in all three genes, while the majority of isolated proviruses were defective in one or more genes. No intact PERV A proviruses were found in this pig, despite the identification of multiple defective A proviruses. Genotyping of 30 unrelated pigs for these unique proviruses showed a heterogeneous distribution. Two proviruses were uncommon, present in 7 of 30 and 3 of 30 pigs, while three were each present in 24 of 30 pigs, and one was present in 30 of 30 animals examined. Our data indicate that fewPERV proviruses in Large White pigs are capable of productive infection and suggest that many could be removed by selective breeding. Further studies are required to determine if all potentially functional proviruses could be removed by breeding or whether gene knockout techniques will be required to remove the residuum.

[1]  A. Wolffe,et al.  Reprogramming nuclei: insights from cloning, nuclear transfer and heterokaryons. , 2000, Journal of cell science.

[2]  R. Weiss,et al.  Two sets of human-tropic pig retrovirus , 1997, Nature.

[3]  D. Onions,et al.  Endogenous retroviruses and the safety of porcine xenotransplantation. , 1998, Trends in microbiology.

[4]  J. Mullins,et al.  Nucleotide sequences of a feline leukemia virus subgroup A envelope gene and long terminal repeat and evidence for the recombinational origin of subgroup B viruses , 1986, Journal of virology.

[5]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .

[6]  H. Temin,et al.  Effect of gamma radiation on retroviral recombination , 1992, Journal of virology.

[7]  J. Blomberg,et al.  Identification of Novel Porcine Endogenous Betaretrovirus Sequences in Miniature Swine , 2001, Journal of Virology.

[8]  Yasuhiro Takeuchi,et al.  Infection of human cells by an endogenous retrovirus of pigs , 1997, Nature Medicine.

[9]  R. Elliott,et al.  No Evidence of Infection with Porcine Endogenous Retrovirus in Recipients of Encapsulated Porcine Islet Xenografts , 2000, Cell transplantation.

[10]  B. Torbett,et al.  Infection by porcine endogenous retrovirus after islet xenotransplantation in SCID mice , 2000, Nature.

[11]  Melanie E. Goward,et al.  Multiple Groups of Novel Retroviral Genomes in Pigs and Related Species , 2001, Journal of Virology.

[12]  S. Lukyanov,et al.  An improved PCR method for walking in uncloned genomic DNA. , 1995, Nucleic acids research.

[13]  Y. Takeuchi,et al.  A conserved mechanism of retrovirus restriction in mammals. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[14]  Y. Takeuchi,et al.  Productive infection of primary human endothelial cells by pig endogenous retrovirus (PERV) , 2000, Xenotransplantation.

[15]  W. Heneine,et al.  No evidence of infection with porcine endogenous retrovirus in recipients of porcine islet-cell xenografts , 1998, The Lancet.

[16]  Prof. Dr. med. Gustav Steinhoff,et al.  Analysis of potential porcine endogenous retrovirus (PERV) transmission in a whole-organ xenotransplantation model without interfering microchimerism , 2001, Transplant international : official journal of the European Society for Organ Transplantation.

[17]  C. Porter,et al.  Sensitization of rhabdo-, lenti-, and spumaviruses to human serum by galactosyl(alpha1-3)galactosylation , 1997, Journal of virology.

[18]  A. Jestin,et al.  Study of Full-Length Porcine Endogenous Retrovirus Genomes with Envelope Gene Polymorphism in a Specific-Pathogen-Free Large White Swine Herd , 2000, Journal of Virology.

[19]  T. Kono Nuclear transfer and reprogramming. , 1997, Reviews of reproduction.

[20]  Y Takeuchi,et al.  Infection of Nonhuman Primate Cells by Pig Endogenous Retrovirus , 2000, Journal of Virology.

[21]  X. M. Fernández-Suárez,et al.  Monitoring xenotransplant recipients for infection by PERV. , 2001, Clinical biochemistry.

[22]  Timothy M. Rose,et al.  Type C Retrovirus Released from Porcine Primary Peripheral Blood Mononuclear Cells Infects Human Cells , 1998, Journal of Virology.

[23]  J. Coffin,et al.  The four classes of endogenous murine leukemia virus: structural relationships and potential for recombination , 1987, Journal of virology.

[24]  M. Denaro,et al.  Identification of a Full-Length cDNA for an Endogenous Retrovirus of Miniature Swine , 1998, Journal of Virology.

[25]  Nicole Fischer,et al.  Comparison of Replication-Competent Molecular Clones of Porcine Endogenous Retrovirus Class A and Class B Derived from Pig and Human Cells , 2001, Journal of Virology.

[26]  A. Osterhaus,et al.  An approach to the control of disease transmission in pig‐to‐human xenotransplantation , 2000, Xenotransplantation.

[27]  J. Banchereau,et al.  Liver allotransplantation after extracorporeal hepatic support with transgenic (hCD55/hCD59) porcine livers: clinical results and lack of pig-to-human transmission of the porcine endogenous retrovirus. , 2000, Transplantation.

[28]  O. Isacson,et al.  Transplantation of embryonic porcine mesencephalic tissue in patients with PD , 2000, Neurology.

[29]  C. Mullon,et al.  Evidence of absence of porcine endogenous retrovirus (PERV) infection in patients treated with a bioartificial liver support system. , 1999, Artificial organs.

[30]  R. Weiss,et al.  No evidence of pig DNA or retroviral infection in patients with short-term extracorporeal connection to pig kidneys , 1998, The Lancet.

[31]  R. Weiss,et al.  Host range and interference studies of three classes of pig endogenous retrovirus. , 1999, Journal of virology.

[32]  J. D. den Dunnen,et al.  Protein truncation test (PTT) for rapid detection of translation-terminating mutations. , 1993, Human molecular genetics.

[33]  J. Coffin,et al.  Highly preferred targets for retrovirus integration , 1988, Cell.

[34]  Yifan Dai,et al.  Cloned pigs produced by nuclear transfer from adult somatic cells , 2000, Nature.

[35]  Y. Obata,et al.  Epigenetic modifications during oocyte growth correlates with extended parthenogenetic development in the mouse , 1996, Nature Genetics.

[36]  A Onishi,et al.  Pig cloning by microinjection of fetal fibroblast nuclei. , 2000, Science.

[37]  M. Goddard,et al.  Long-term survival of nonhuman primates receiving life-supporting transgenic porcine kidney xenografts. , 2000, Transplantation.

[38]  R. Weiss,et al.  Infection hazards of xenotransplantation. , 2000, The Journal of infection.

[39]  M. VanBrocklin,et al.  Extended Analysis of the In Vitro Tropism of Porcine Endogenous Retrovirus , 2000, Journal of Virology.

[40]  Alan W Moore,et al.  NO EVIDENCE FOR INFECTION OF HUMAN CELLS WITH PORCINE ENDOGENOUS RETROVIRUS (PERV) AFTER EXPOSURE TO PORCINE FETAL NEURONAL CELLS1 , 2000, Transplantation.

[41]  R. Kurth,et al.  Genome-Wide Screening, Cloning, Chromosomal Assignment, and Expression of Full-Length Human Endogenous Retrovirus Type K , 1999, Journal of Virology.

[42]  W. Rawlinson,et al.  TRANSMISSION OF PORCINE ENDOGENOUS RETROVIRUSES IN SEVERE COMBINED IMMUNODEFICIENT MICE XENOTRANSPLANTED WITH FETAL PORCINE PANCREATIC CELLS1 , 2000, Transplantation.

[43]  J. Coffin,et al.  The dangers of xenotransplantation , 1995, Nature Medicine.

[44]  W. Heneine,et al.  Search for cross-species transmission of porcine endogenous retrovirus in patients treated with living pig tissue. The XEN 111 Study Group. , 1999, Science.

[45]  B. Lapin,et al.  Porcine endogenous retrovirus (PERV) was not transmitted from transplanted porcine endothelial cells to baboons in vivo , 1998, Transplant international : official journal of the European Society for Organ Transplantation.

[46]  M. Pfister-Genskow,et al.  Production of cloned pigs from in vitro systems , 2000, Nature Biotechnology.