Tsl and LP-BM5: a comparison of two murine retrovirus models for HIV.

The ts1 murine leukemia virus produces an immunodeficiency state in mice that parallels human immunodeficiency virus (HIV) infection in humans. Other murine leukemia viruses, such as LP-BM5 used in the murine acquired immune deficiency virus (MAIDS) model, have been studied extensively as a small animal model for HIV research, but lack many key similarities to HIV. Mice infected with ts1, however, utilize CD4 target cells for infection, undergo neuronal loss and demyelination, and develop clinical immunodeficiency. These features make this retrovirus in many ways an ideal candidate for a small animal model for HIV research. In this review article, the early development, the molecular and clinical pathogenesis of both the ts1 mutant of the Moloney murine leukemia virus and LP-BM5 are examined. Based on an extensive evaluation of the literature on LP-BM5 and ts1, it is concluded that the ts1 virus may serve as a better animal model to human retrovirus infection.

[1]  Y. Kubo,et al.  Induction of B-Cell Lymphoma in BALB/c Nude Mice with an Ecotropic, B-Tropic Helper Virus Present in the Murine AIDS Virus Stock , 1999, Journal of Virology.

[2]  W. Lynn,et al.  Neuroimmunopathogenesis of ts1 MoMuLV Viral Infection , 1998, Neuroimmunomodulation.

[3]  P. Linsley,et al.  CD28-B7 Costimulatory Blockade by CTLA4Ig Delays the Development of Retrovirus-Induced Murine AIDS , 1998, Journal of Virology.

[4]  P. Jolicoeur,et al.  Establishment of MAIDS-defective virus-infected B cell lines and their characterization. , 1998, Virology.

[5]  R. Noelle,et al.  Evidence for a continued requirement for CD40/CD40 ligand (CD154) interactions in the progression of LP-BM5 retrovirus-induced murine AIDS. , 1998, Virology.

[6]  G. Stoica,et al.  Neurodegeneration induced by MoMuLV-ts1 and increased expression of Fas and TNF-α in the central nervous system , 1998, Brain Research.

[7]  A. Basile,et al.  LP-BM5 MuLV Infection: Impact on the Immune and Central Nervous Systems , 1998 .

[8]  P. K. Wong,et al.  Development of pathological lesions in the central nervous system of transgenic mice expressing the env gene of ts1 Moloney murine leukemia virus in the absence of the viral gag and pol genes and viral replication. , 1997, Journal of neurovirology.

[9]  M. Barinaga Forging a Path to Cell Death , 1996, Science.

[10]  G. Evan,et al.  A License to Kill , 1996, Cell.

[11]  T. Foy,et al.  Antibody to the ligand for CD40 (gp39) inhibits murine AIDS-associated splenomegaly, hypergammaglobulinemia, and immunodeficiency in disease-susceptible C57BL/6 mice , 1996, Journal of virology.

[12]  K. Saha,et al.  Long-term cultivation and productive infection of primary thymocyte cultures by a thymocytopathic murine retrovirus. , 1996, Virology.

[13]  W. Lynn,et al.  Neuroimmunodegeneration: do neurons and T cells use common pathways for cell death? , 1995, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[14]  V. Metelev,et al.  Induction of apoptosis in uninfected lymphocytes by HIV-1 Tat protein. , 1995, Science.

[15]  J. Levy,et al.  HIV and the Pathogenesis of AIDS , 1994, Nature Medicine.

[16]  P. K. Wong,et al.  Cell types in the central nervous system infected by murine retroviruses: implications for the mechanisms of neurodegeneration. , 1994, Histology and histopathology.

[17]  K. Saha,et al.  Murine retrovirus-induced depletion of T cells is mediated through activation-induced death by apoptosis , 1994, Journal of virology.

[18]  J. Glass,et al.  Intracerebral cytokine messenger RNA expression in acquired immunodeficiency syndrome dememtia , 1993, Annals of neurology.

[19]  B. Brooks,et al.  Correlation of specific virus-astrocyte interactions and cytopathic effects induced by ts1, a neurovirulent mutant of Moloney murine leukemia virus , 1993, Journal of virology.

[20]  H. Morse,et al.  Retrovirus-induced immunodeficiency in the mouse: MAIDS as a model for AIDS. , 1992, AIDS.

[21]  K. Saha,et al.  ts1, a temperature-sensitive mutant of Moloney murine leukemia virus TB, can infect both CD4+ and CD8+ T cells but requires CD4+ T cells in order to cause paralysis and immunodeficiency , 1992, Journal of virology.

[22]  G. Stoica,et al.  Temporal lymphoreticular changes caused by ts1, a paralytogenic mutant of Moloney murine leukemia virus TB. , 1992, Laboratory investigation; a journal of technical methods and pathology.

[23]  B. Brooks,et al.  Murine leukemia virus induced central nervous system diseases. , 1992, Leukemia.

[24]  M. Cuénod,et al.  Murine brain macrophages induce NMDA receptor mediated neurotoxicity in vitro by secreting glutamate , 1991, Neuroscience Letters.

[25]  P. K. Wong,et al.  Alteration from T- to B-cell tropism reduces thymic atrophy and cytocidal effects in thymocytes but not neurovirulence induced by ts1, a mutant of Moloney murine leukemia virus TB. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[26]  P. Jolicoeur Murine acquired immunodeficiency syndrome (MAIDS): an animal model to study the AIDS pathogenesis , 1991, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[27]  P. Szurek,et al.  High susceptibility of FVB/N mice to the paralytic disease induced by ts1, a mutant of Moloney murine leukemia virus TB. , 1991, Virology.

[28]  N. Alexander,et al.  Sexual transmission of human immunodeficiency virus: virus entry into the male and female genital tract. World Health Organization, Global Programme on Acquired Immune Deficiency Syndrome. , 1990, Fertility and sterility.

[29]  J. Ball,et al.  A Val-25-to-Ile substitution in the envelope precursor polyprotein, gPr80env, is responsible for the temperature sensitivity, inefficient processing of gPr80env, and neurovirulence of ts1, a mutant of Moloney murine leukemia virus TB , 1990, Journal of virology.

[30]  P. Wong,et al.  Moloney murine leukemia virus temperature-sensitive mutants: a model for retrovirus-induced neurologic disorders. , 1990, Current topics in microbiology and immunology.

[31]  P. Jolicoeur,et al.  Immunodeficiency and clonal growth of target cells induced by helper-free defective retrovirus. , 1989, Science.

[32]  J. Hansen,et al.  ts1, a mutant of Moloney murine leukemia virus-TB, causes both immunodeficiency and neurologic disorders in BALB/c mice. , 1989, Virology.

[33]  H. Morse,et al.  Defective virus is associated with induction of murine retrovirus-induced immunodeficiency syndrome. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[34]  P. Jolicoeur,et al.  Severe immunodeficiency disease induced by a defective murine leukaemia virus , 1989, Nature.

[35]  G. Stoica,et al.  The role of the thymus in the pathogenesis of hind-limb paralysis induced by ts1, a mutant of Moloney murine leukemia virus-TB. , 1989, Virology.

[36]  H. Morse,et al.  Retrovirus-induced murine acquired immunodeficiency syndrome: natural history of infection and differing susceptibility of inbred mouse strains , 1989, Journal of virology.

[37]  S. Klinken,et al.  Evolution of B cell lineage lymphomas in mice with a retrovirus-induced immunodeficiency syndrome, MAIDS. , 1988, Journal of immunology.

[38]  D. Malehorn,et al.  Molecular cloning of two paralytogenic, temperature-sensitive mutants, ts1 and ts7, and the parental wild-type Moloney murine leukemia virus , 1985, Journal of virology.

[39]  H. Morse,et al.  Retroviral induction of acute lymphoproliferative disease and profound immunosuppression in adult C57BL/6 mice , 1985, The Journal of experimental medicine.

[40]  G. Gallick,et al.  A group of temperature-sensitive mutants of Moloney leukemia virus which is defective in cleavage of env precursor polypeptide in infected cells also induces hind-limb paralysis in newborn CFW/D mice. , 1983, Virology.

[41]  M. Haas,et al.  Immunopathology of B-cell lymphomas induced in C57BL/6 mice by dualtropic murine leukemia virus (MuLV). , 1982, The American journal of pathology.

[42]  M. Haas,et al.  Involvement of peritoneal macrophages and spleen stromal cells in X-irradiation-induced reticulum cell neoplasms in C57BL/6 mice. , 1982, Leukemia research.

[43]  A. Meshorer,et al.  Reticulum cell neoplasms induced in C57BL/6 mice by cultured virus grown in stromal hematopoietic cell lines. , 1979, Journal of the National Cancer Institute.

[44]  B. Guillemain,et al.  Characterization by molecular hybridization of two viral populations derived from a radiation leukemia virus. , 1978, Cancer research.

[45]  J. Ball,et al.  Lower limb paralysis induced in mice by a temperature-sensitive mutant of Moloney leukemia virus. , 1977, Journal of the National Cancer Institute.

[46]  J. McCarter,et al.  Studies of two temperature-sensitive mutants of Moloney murine leukemia virus. , 1974, Virology.

[47]  J. McCarter,et al.  Rapid, selective procedure for isolation of spontaneous temperature-sensitive mutants of Moloney leukemia virus. , 1973, Virology.

[48]  T. Dunn,et al.  Reticulum cell neoplasm, type B, or the "Hodgkin's-like lesion" of the mouse. , 1968, Journal of the National Cancer Institute.

[49]  R. Latarjet,et al.  Studies on the mechanism of radiation-induced leukemogenesis in C57BL mice. , 1966, Cancer research.

[50]  R. Latarjet,et al.  Experiment and discussion on leukaemogenesis by cell-free extracts of radiation-induced leukaemia in mice. , 1962, International journal of radiation biology and related studies in physics, chemistry, and medicine.

[51]  J. Moloney Biological studies on a lymphoid-leukemia virus extracted from sarcoma 37. I. Origin and introductory investigations. , 1960, Journal of the National Cancer Institute.