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1. McGee-Estrada K, Palmarini M, Hallwirth C, Fan H: A Moloney murine leukemia virus driven by the Jaagsiekte sheep retrovirus enhancers shows enhanced specificity for infectivity in lung epithelial cells. Virus Genes; 2005 Dec;31(3):257-63
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Jaagsiekte sheep retrovirus (JSRV) is the etiologic agent of ovine pulmonary adenocarcinoma (OPA), a transmissible lung cancer in sheep.
  • One of the unique features of this virus is that in infected animals, the only tissues that show expression of the virus are the tumor cells in the lung.
  • Transient transfection assays indicated that the DeltaMo + JS LTR is > 5-fold more active in lung epithelial cell lines than in non-lung lines, compared to the wild-type M-MuLV LTR.
  • [MeSH-minor] Animals. Cell Line. Enhancer Elements, Genetic. Epithelial Cells / virology. Genes, Viral. Mice. Plasmids / genetics. Pulmonary Adenomatosis, Ovine / etiology. Pulmonary Adenomatosis, Ovine / virology. Sheep. Terminal Repeat Sequences. Transfection. Virulence / genetics

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  • (PMID = 16175331.001).
  • [ISSN] 0920-8569
  • [Journal-full-title] Virus genes
  • [ISO-abbreviation] Virus Genes
  • [Language] eng
  • [Grant] United States / NCI NIH HHS / CA / CA85264; United States / NCI NIH HHS / CA / T32 CA09054
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
  • [Publication-country] United States
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2. McGee-Estrada K, Fan H: In vivo and in vitro analysis of factor binding sites in Jaagsiekte sheep retrovirus long terminal repeat enhancer sequences: roles of HNF-3, NF-I, and C/EBP for activity in lung epithelial cells. J Virol; 2006 Jan;80(1):332-41
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  • Jaagsiekte sheep retrovirus (JSRV) is the causative agent of ovine pulmonary adenocarcinoma, a contagious lung cancer of sheep that arises from type II pneumocytes and Clara cells of the lung epithelium.
  • To map regulatory regions important for transcriptional activation, an in vivo footprinting method that couples dimethyl sulfate treatment and ligation-mediated PCR was performed in murine type II pneumocyte-derived MLE-15 cells infected with a chimeric Moloney murine leukemia virus driven by the JSRV enhancers (DeltaMo+JS Mo-MuLV).

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  • (PMID = 16352558.001).
  • [ISSN] 0022-538X
  • [Journal-full-title] Journal of virology
  • [ISO-abbreviation] J. Virol.
  • [Language] ENG
  • [Grant] United States / NCI NIH HHS / CA / T32 CA009054; United States / NCI NIH HHS / CA / R01 CA82654; United States / PHS HHS / / T32A09054
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / CCAAT-Enhancer-Binding Proteins; 0 / NF-kappa B; 0 / Transcription Factors; 135845-92-0 / Hepatocyte Nuclear Factor 3-beta
  • [Other-IDs] NLM/ PMC1317537
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3. Rosati S, Pittau M, Alberti A, Pozzi S, York DF, Sharp JM, Palmarini M: An accessory open reading frame (orf-x) of jaagsiekte sheep retrovirus is conserved between different virus isolates. Virus Res; 2000 Jan;66(1):109-16
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Jaagsiekte sheep retrovirus (JSRV) is the etiological agent of a contagious lung tumour of sheep known as sheep pulmonary adenomatosis (syn: ovine pulmonary carcinoma, jaagsiekte).
  • JSRV exhibits a simple genetic organization, characteristic of the type D and type B retroviruses, with the canonical retroviral sequences gag, pro, pol and env encoding the structural proteins of the virion.
  • Thus orf-x may be an accessory gene of JSRV and haves a biological function which might be advantageous to JSRV.
  • [MeSH-major] Betaretrovirus / genetics. Betaretrovirus / isolation & purification. Open Reading Frames / genetics. Pulmonary Adenomatosis, Ovine / virology
  • [MeSH-minor] Animals. DNA, Viral / analysis. DNA, Viral / genetics. Lung / virology. Molecular Sequence Data. Phylogeny. Polymerase Chain Reaction. Polymorphism, Genetic. Sequence Analysis, DNA. Sheep

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  • (PMID = 10653922.001).
  • [ISSN] 0168-1702
  • [Journal-full-title] Virus research
  • [ISO-abbreviation] Virus Res.
  • [Language] eng
  • [Databank-accession-numbers] GENBANK/ AF128917/ AF128918/ AF128919/ AF128920/ AF128921/ AF128922/ AF128923/ AF128924/ AF128925/ AF128926/ AF129876/ AF129877/ AF129878/ AF129879/ AF129880/ AF136851/ AF136852/ AF136853/ AF136854
  • [Publication-type] Journal Article
  • [Publication-country] NETHERLANDS
  • [Chemical-registry-number] 0 / DNA, Viral
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4. McGee-Estrada K, Palmarini M, Fan H: HNF-3beta is a critical factor for the expression of the Jaagsiekte sheep retrovirus long terminal repeat in type II pneumocytes but not in Clara cells. Virology; 2002 Jan 5;292(1):87-97
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  • [Title] HNF-3beta is a critical factor for the expression of the Jaagsiekte sheep retrovirus long terminal repeat in type II pneumocytes but not in Clara cells.
  • Jaagsiekte sheep retrovirus (JSRV) is the causative agent of ovine pulmonary adenocarcinoma (OPA), a sheep lung cancer that resembles human lung adenocarcinoma or bronchioloaveolar carcinoma (BAC).
  • JSRV is the only retrovirus that shows lung tropism and induces pulmonary carcinoma.
  • In murine MLE-15 cells (derived from type II pneumocytes), mutations within the upstream site (minus sign147 to minus sign128 bp) resulted in a 72% reduction of the LTR activity, while mutation of the downstream site had little effect.
  • [MeSH-major] DNA-Binding Proteins / metabolism. Gene Expression Regulation, Viral. Jaagsiekte sheep retrovirus / pathogenicity. Nuclear Proteins / metabolism. Pulmonary Adenomatosis, Ovine / virology. Terminal Repeat Sequences / physiology. Transcription Factors
  • [MeSH-minor] 3T3 Cells. Animals. Base Sequence. Cell Line. Hepatocyte Nuclear Factor 3-beta. Lung / cytology. Lung / virology. Mice. Molecular Sequence Data. Sheep. Transcription, Genetic

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  • (PMID = 11878911.001).
  • [ISSN] 0042-6822
  • [Journal-full-title] Virology
  • [ISO-abbreviation] Virology
  • [Language] eng
  • [Grant] United States / NCI NIH HHS / CA / R01CA 82564; United States / NCI NIH HHS / CA / T32 CA09054
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / DNA-Binding Proteins; 0 / Foxa2 protein, mouse; 0 / Nuclear Proteins; 0 / Transcription Factors; 135845-92-0 / Hepatocyte Nuclear Factor 3-beta
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5. De Las Heras M, Ortín A, Benito A, Summers C, Ferrer LM, Sharp JM: In-situ demonstration of mitogen-activated protein kinase Erk 1/2 signalling pathway in contagious respiratory tumours of sheep and goats. J Comp Pathol; 2006 Jul;135(1):1-10
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Ovine pulmonary adenocarcinoma (OPA) and enzootic nasal adenocarcinoma (ENA) are two contagious neoplastic diseases of secretory epithelial cells in the respiratory system of sheep and goats.
  • Jaagsiekte sheep retrovirus (JSRV) is the aetiological agent of OPA, and enzootic nasal tumour virus (ENTV) is associated with ENA.
  • The genomes of these retroviruses do not contain known oncogenes but products of the env gene are important in the generation of transforming stimuli.
  • This study was based on the use of activation stage antibodies specifically detecting proteins of the extracellular signal regulated kinase Erk 1/2 cell signalling pathway and transcription factors.
  • Representative proteins of the Erk1/2 pathway (Raf-1, Mek1/2 and p44/42MAPK) were activated in natural cases of OPA and ENA in sheep and goats and also in experimentally induced OPA.
  • [MeSH-major] Adenocarcinoma / veterinary. Mitogen-Activated Protein Kinase 1 / metabolism. Mitogen-Activated Protein Kinase 3 / metabolism. Nose Neoplasms / enzymology. Nose Neoplasms / veterinary. Pulmonary Adenomatosis, Ovine / enzymology. Pulmonary Adenomatosis, Ovine / pathology. Signal Transduction
  • [MeSH-minor] Animals. Goats. Immunohistochemistry / veterinary. Jaagsiekte sheep retrovirus / pathogenicity. Models, Biological. Neoplasms, Experimental / enzymology. Neoplasms, Experimental / pathology. Neoplasms, Experimental / virology. Sheep. Transcription Factors / genetics. Transcription Factors / metabolism


6. Summers C, Neill W, Dewar P, Gonzalez L, van der Molen R, Norval M, Sharp JM: Systemic immune responses following infection with Jaagsiekte sheep retrovirus and in the terminal stages of ovine pulmonary adenocarcinoma. J Gen Virol; 2002 Jul;83(Pt 7):1753-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Systemic immune responses following infection with Jaagsiekte sheep retrovirus and in the terminal stages of ovine pulmonary adenocarcinoma.
  • Jaagsiekte sheep retrovirus (JSRV) is the aetiological agent of ovine pulmonary adenocarcinoma (OPA).
  • In contrast, reduced responses to concanavalin A stimulation were demonstrated in the JSRV-inoculated lambs, prior to the onset of clinical disease, and also in the terminally ill adult sheep.
  • [MeSH-major] Jaagsiekte sheep retrovirus. Pulmonary Adenomatosis, Ovine / immunology. Sheep / immunology
  • [MeSH-minor] Animals. CD4 Lymphocyte Count. CD4-Positive T-Lymphocytes / immunology. Cell Division / drug effects. Immunity, Cellular. Leukocytes, Mononuclear / immunology. Lymphopenia / pathology. Neutropenia / pathology. Phytohemagglutinins / pharmacology. Pokeweed Mitogens / pharmacology

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  • (PMID = 12075095.001).
  • [ISSN] 0022-1317
  • [Journal-full-title] The Journal of general virology
  • [ISO-abbreviation] J. Gen. Virol.
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Phytohemagglutinins; 0 / Pokeweed Mitogens
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7. Ortín A, Pérez de Villarreal M, Minguijón E, Cousens C, Sharp JM, De las Heras M: Coexistence of enzootic nasal adenocarcinoma and jaagsiekte retrovirus infection in sheep. J Comp Pathol; 2004 Nov;131(4):253-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Ten sheep naturally affected with enzootic nasal adenocarcinoma (ENA), a disease associated with ovine enzootic nasal tumour virus (ENTV-1), were found also to be infected with jaagsiekte sheep retrovirus (JSRV), the causal agent of ovine pulmonary adenocarcinoma (OPA).
  • The animals belonged to 10 flocks located in a geographical area in which OPA is frequently seen.
  • In contrast, JSRV had a disseminated tissue distribution, similar to that previously reported for animals infected with JSRV.
  • [MeSH-major] Adenocarcinoma / veterinary. Jaagsiekte sheep retrovirus / physiology. Neoplasms, Multiple Primary / veterinary. Nose Neoplasms / veterinary. Pulmonary Adenomatosis, Ovine / pathology
  • [MeSH-minor] Animals. DNA, Viral / analysis. Female. Lymph Nodes / pathology. Lymph Nodes / virology. Polymerase Chain Reaction / methods. Polymerase Chain Reaction / veterinary. Sheep

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  • (PMID = 15511533.001).
  • [ISSN] 0021-9975
  • [Journal-full-title] Journal of comparative pathology
  • [ISO-abbreviation] J. Comp. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] 0 / DNA, Viral
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8. Archer F, Jacquier E, Lyon M, Chastang J, Cottin V, Mornex JF, Leroux C: Alveolar type II cells isolated from pulmonary adenocarcinoma: a model for JSRV expression in vitro. Am J Respir Cell Mol Biol; 2007 May;36(5):534-40
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Alveolar type II cells isolated from pulmonary adenocarcinoma: a model for JSRV expression in vitro.
  • Ovine pulmonary adenocarcinoma (OPA) is a naturally occurring cancer in sheep, with clinical, radiologic, and histopathologic features similar to that of human pneumonic-type bronchioloalveolar carcinoma.
  • JSRV (Jaagsiekte Sheep RetroVirus) is the etiologic agent of this contagious lung cancer in sheep.
  • Cells involved in the tumor derive from alveolar type II cells and Clara cells, epithelial cells of the distal respiratory tract.
  • These cells are the major site for viral expression in JSRV-infected animals.
  • Interestingly, the cellular pathways involved in the transformation process seem to be dependent of the origin and type of the cell used.
  • In order to investigate the specific interactions between JSRV and alveolar type II cells, we developed an in vitro experimental model in which lung epithelial cells were isolated from OPA and control lungs.
  • Cells in culture expressed alveolar type II cell specific markers such as surfactant protein (SP)-A, SP-C, and a high alkaline phosphatase activity.
  • Alveolar Type II cells derived from tumoral lungs showed a proliferative advantage and expressed the JSRV virus.
  • We thus report on the first in vitro system whereby alveolar type II cells from OPA were efficiently maintained in culture and stably expressed JSRV.
  • [MeSH-major] Jaagsiekte sheep retrovirus / genetics. Lung Neoplasms / veterinary. Pulmonary Adenomatosis, Ovine / virology. Pulmonary Alveoli / pathology. Pulmonary Alveoli / virology
  • [MeSH-minor] Animals. Biomarkers / metabolism. Cell Aging. Cell Separation. Cells, Cultured. DNA, Viral / analysis. DNA, Viral / genetics. Gene Expression Regulation, Viral. Models, Biological. Pulmonary Surfactant-Associated Protein A / metabolism. Pulmonary Surfactant-Associated Protein C / metabolism. RNA-Directed DNA Polymerase / metabolism. Serial Passage. Sheep, Domestic

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  • (PMID = 17158359.001).
  • [ISSN] 1044-1549
  • [Journal-full-title] American journal of respiratory cell and molecular biology
  • [ISO-abbreviation] Am. J. Respir. Cell Mol. Biol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers; 0 / DNA, Viral; 0 / Pulmonary Surfactant-Associated Protein A; 0 / Pulmonary Surfactant-Associated Protein C; EC 2.7.7.49 / RNA-Directed DNA Polymerase
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9. Palmarini M, Fan H: Molecular biology of jaagsiekte sheep retrovirus. Curr Top Microbiol Immunol; 2003;275:81-115
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Jaagsiekte sheep retrovirus (JSRV) is the causative agent of ovine pulmonary adenocarcinoma (OPA), a contagious lung cancer of sheep.
  • [MeSH-minor] Base Sequence. Binding Sites. Cells, Cultured. Cloning, Molecular / methods. Gene Expression Regulation, Viral. Models, Genetic. Phylogeny. Pulmonary Adenomatosis, Ovine / virology. RNA, Messenger / genetics. Sequence Homology

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  • (PMID = 12596896.001).
  • [ISSN] 0070-217X
  • [Journal-full-title] Current topics in microbiology and immunology
  • [ISO-abbreviation] Curr. Top. Microbiol. Immunol.
  • [Language] eng
  • [Grant] United States / NCI NIH HHS / CA / CA95706-01
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.; Review
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / RNA, Messenger
  • [Number-of-references] 121
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10. Nakanishi K, Matsuo H, Kanai Y, Endou H, Hiroi S, Tominaga S, Mukai M, Ikeda E, Ozeki Y, Aida S, Kawai T: LAT1 expression in normal lung and in atypical adenomatous hyperplasia and adenocarcinoma of the lung. Virchows Arch; 2006 Feb;448(2):142-50
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  • No previous study has investigated neutral large amino acid transporter type 1 (LAT1) in normal lung cells, or in atypical adenomatous hyperplasia(s) (AAH) and nonmucinous bronchioloalveolar carcinoma(s) (NMBAC) of the lung.
  • In peripheral normal lung tissues, LAT1 mRNA and protein were detected in bronchial surface epithelial cells and alveolar macrophages (but not in nonciliated bronchiolar epithelial cells, or in alveolar type I or type II cells).
  • In bronchial surface epithelial cells, LAT1 protein appeared to be of a nodular type, which was considered to be a nonfunctional protein pattern.
  • [MeSH-major] Adenocarcinoma, Bronchiolo-Alveolar / pathology. Adenomatosis, Pulmonary / pathology. Large Neutral Amino Acid-Transporter 1 / genetics. Lung / metabolism. Lung Neoplasms / pathology

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  • (PMID = 16175382.001).
  • [ISSN] 0945-6317
  • [Journal-full-title] Virchows Archiv : an international journal of pathology
  • [ISO-abbreviation] Virchows Arch.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Ki-67 Antigen; 0 / Large Neutral Amino Acid-Transporter 1; 0 / RNA, Messenger
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11. Lee GH, Matsushita H, Kitagawa T: Fine chromosomal localization of the mouse Par2 gene that confers resistance against urethane-induction of pulmonary adenomas. Oncogene; 2001 Jul 5;20(30):3979-85
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  • [Title] Fine chromosomal localization of the mouse Par2 gene that confers resistance against urethane-induction of pulmonary adenomas.
  • BALB/cByJ mice are 14 times more resistant to urethane-induction of pulmonary adenomas than the susceptible A/J strain.
  • Our previous linkage analysis of (A/J x BALB/cByJ)F1 x A/J backcross mice provided statistical evidence that a major resistance locus of BALB/cByJ with a dominant effect, designated Par2 (Pulmonary adenoma resistance 2), exists within an approximately 25 cM section of distal chromosome 18.
  • This backcross-selection cycle was simply repeated to produce semi-congenic mice with a general BALB/cByJ genetic background except for the Par2 interval, where the mice were heterozygous with paternal C57BL/6J alleles and maternal BALB/cByJ alleles.
  • [MeSH-major] Adenomatosis, Pulmonary / chemically induced. Carcinogens / toxicity. Genes, Tumor Suppressor. Lung Neoplasms / chemically induced. Mice / genetics. Urethane / toxicity
  • [MeSH-minor] Animals. Animals, Congenic. Chromosome Mapping. Crosses, Genetic. Drug Resistance / genetics. Female. Genetic Linkage. Genotype. Immunity, Innate / genetics. Male. Mice, Inbred A. Mice, Inbred BALB C. Mice, Inbred C57BL. Microsatellite Repeats. Quantitative Trait, Heritable

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  • (PMID = 11494126.001).
  • [ISSN] 0950-9232
  • [Journal-full-title] Oncogene
  • [ISO-abbreviation] Oncogene
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Carcinogens; 3IN71E75Z5 / Urethane
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12. Caporale M, Centorame P, Giovannini A, Sacchini F, Di Ventura M, De las Heras M, Palmarini M: Infection of lung epithelial cells and induction of pulmonary adenocarcinoma is not the most common outcome of naturally occurring JSRV infection during the commercial lifespan of sheep. Virology; 2005 Jul 20;338(1):144-53
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  • [Title] Infection of lung epithelial cells and induction of pulmonary adenocarcinoma is not the most common outcome of naturally occurring JSRV infection during the commercial lifespan of sheep.
  • Jaagsiekte sheep retrovirus (JSRV) is the causative agent of ovine pulmonary adenocarcinoma (OPA).
  • We established groups derived from flocks with either a high or low incidence of OPA and monitored virus transmission, clinical disease and macroscopic/microscopic lung lesions at necropsy.
  • (ii) only a minority of JSRV-infected animals develop clinical disease during their commercial lifespan; and (iii) JSRV is more readily detectable in peripheral blood leucocytes and lymphoid organs than in the lungs.
  • These data support a model of opportunistic JSRV infection and tumorigenic conversion of type II pneumocytes/Clara cells in the lungs, while lymphoreticular cells serve as the principal virus reservoir.
  • [MeSH-major] Adenocarcinoma / veterinary. Jaagsiekte sheep retrovirus / pathogenicity. Lung Neoplasms / veterinary. Pulmonary Adenomatosis, Ovine / etiology. Sheep Diseases / etiology
  • [MeSH-minor] Animals. Animals, Newborn. DNA, Viral / genetics. DNA, Viral / isolation & purification. Epithelial Cells / pathology. Epithelial Cells / virology. Female. Lung / pathology. Lung / virology. Opportunistic Infections / etiology. Opportunistic Infections / veterinary. Opportunistic Infections / virology. Pregnancy. Sheep

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  • (PMID = 15950254.001).
  • [ISSN] 0042-6822
  • [Journal-full-title] Virology
  • [ISO-abbreviation] Virology
  • [Language] eng
  • [Grant] United States / NCI NIH HHS / CA / CA95706-01
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / DNA, Viral
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13. Summers C, Dewar P, van der Molen R, Cousens C, Salvatori D, Sharp JM, Griffiths DJ, Norval M: Jaagsiekte sheep retrovirus-specific immune responses induced by vaccination: a comparison of immunisation strategies. Vaccine; 2006 Mar 10;24(11):1821-9
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  • Jaagsiekte sheep retrovirus (JSRV) is the aetiological agent of ovine pulmonary adenocarcinoma (OPA).
  • The aim of the present study was to induce immune responses in sheep against JSRV proteins using several immunisation strategies.
  • The vaccines were administered subcutaneously and intradermally, or intranasally, in adjuvant.
  • Antibodies specific for JSRV-capsid protein were induced by inoculation of recombinant proteins in adjuvant, and transient JSRV-specific T cell responses by intranasal inoculation with inactivated virus.
  • These results will help in the design of a protective vaccine against JSRV infection and the development of OPA.
  • [MeSH-major] Jaagsiekte sheep retrovirus / immunology. Pulmonary Adenomatosis, Ovine / prevention & control. Vaccination / methods
  • [MeSH-minor] Adjuvants, Immunologic. Administration, Intranasal. Animals. Antibodies, Viral / blood. Blotting, Western. Enzyme-Linked Immunosorbent Assay. Freund's Adjuvant / administration & dosage. Injections, Intradermal. Injections, Subcutaneous. Lipids / administration & dosage. Lymphocyte Activation. Sheep. T-Lymphocytes / immunology. Vaccines, Subunit / administration & dosage. Vaccines, Subunit / genetics. Vaccines, Subunit / immunology. Vaccines, Synthetic / administration & dosage. Vaccines, Synthetic / immunology. Viral Proteins / administration & dosage. Viral Proteins / genetics. Viral Proteins / immunology

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  • (PMID = 16289765.001).
  • [ISSN] 0264-410X
  • [Journal-full-title] Vaccine
  • [ISO-abbreviation] Vaccine
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Netherlands
  • [Chemical-registry-number] 0 / Adjuvants, Immunologic; 0 / Antibodies, Viral; 0 / Lipids; 0 / Vaccines, Subunit; 0 / Vaccines, Synthetic; 0 / Viral Proteins; 0 / incomplete Freund's adjuvant; 9007-81-2 / Freund's Adjuvant
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14. Kozuki T, Hisamoto A, Tabata M, Takigawa N, Kiura K, Segawa Y, Nakata M, Mandai K, Eguchi K, Ueoka H, Tanimoto M: Mutation of the epidermal growth factor receptor gene in the development of adenocarcinoma of the lung. Lung Cancer; 2007 Oct;58(1):30-5
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  • Recently, a mutation of the epidermal growth factor receptor (EGFR) gene has been reported to be implicated in the development of pulmonary adenocarcinoma.
  • [MeSH-major] Adenocarcinoma / genetics. Adenomatosis, Pulmonary / genetics. Genes, erbB-1. Lung Neoplasms / genetics. Mutation. Neoplasms, Multiple Primary / genetics. Receptor, Epidermal Growth Factor / genetics
  • [MeSH-minor] Antineoplastic Agents / therapeutic use. Drug Resistance, Neoplasm. Exons. Female. Genetic Predisposition to Disease. Humans. Male. Quinazolines / therapeutic use. Retrospective Studies

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  • (PMID = 17561305.001).
  • [ISSN] 0169-5002
  • [Journal-full-title] Lung cancer (Amsterdam, Netherlands)
  • [ISO-abbreviation] Lung Cancer
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Ireland
  • [Chemical-registry-number] 0 / Antineoplastic Agents; 0 / Quinazolines; EC 2.7.10.1 / Receptor, Epidermal Growth Factor; S65743JHBS / gefitinib
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15. Dakessian RM, Inoshima Y, Fan H: Tumors in mice transgenic for the envelope protein of Jaagsiekte sheep retrovirus. Virus Genes; 2007 Aug;35(1):73-80
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Jaagsiekte sheep retrovirus (JSRV) is the causative agent of ovine pulmonary adenocarcinoma (OPA), a contagious lung cancer in sheep.
  • [MeSH-major] Adenocarcinoma / genetics. Genes, env. Jaagsiekte sheep retrovirus / genetics. Lung Neoplasms / genetics. Pulmonary Adenomatosis, Ovine / genetics
  • [MeSH-minor] Animals. Disease Models, Animal. Embryo, Mammalian. Female. Mice. Mice, Inbred BALB C. Mice, Inbred C57BL. Mice, Transgenic. Models, Biological. Pregnancy. Sheep

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  • (PMID = 17043760.001).
  • [ISSN] 0920-8569
  • [Journal-full-title] Virus genes
  • [ISO-abbreviation] Virus Genes
  • [Language] eng
  • [Grant] United States / PHS HHS / / 82564; United States / NCI NIH HHS / CA / CA94188
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural
  • [Publication-country] United States
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16. Palmarini M, Murgia C, Fan H: Spliced and prematurely polyadenylated Jaagsiekte sheep retrovirus-specific RNAs from infected or transfected cells. Virology; 2002 Mar 1;294(1):180-8
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  • Jaagsiekte sheep retrovirus (JSRV) is the etiologic agent of a contagious lung cancer of sheep, ovine pulmonary adenocarcinoma (OPA).
  • The orf-x gene of the virus appears to be expressed from two singly spliced subgenomic mRNAs of 3.2 kb that would encode an independent orf-x protein of 179 amino acids.
  • [MeSH-major] Jaagsiekte sheep retrovirus / pathogenicity. Pulmonary Adenomatosis, Ovine / virology. RNA Splicing. RNA, Messenger / metabolism. RNA, Viral / metabolism. Transfection
  • [MeSH-minor] Animals. Base Sequence. Cell Line. Molecular Sequence Data. Polyadenylation. Sheep

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  • [Copyright] (C)2002 Elsevier Science (USA).
  • (PMID = 11886276.001).
  • [ISSN] 0042-6822
  • [Journal-full-title] Virology
  • [ISO-abbreviation] Virology
  • [Language] eng
  • [Grant] United States / NCI NIH HHS / CA / R01 CA 82564
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / RNA, Messenger; 0 / RNA, Viral
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17. Varela M, Spencer TE, Palmarini M, Arnaud F: Friendly viruses: the special relationship between endogenous retroviruses and their host. Ann N Y Acad Sci; 2009 Oct;1178:157-72
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  • The sheep genome contains 27 endogenous retroviruses (enJSRVs) related to the pathogenic Jaagsiekte sheep retrovirus (JSRV), the causative agent of a transmissible lung cancer in sheep. enJSRVs are able to protect their host against JSRV infection by blocking different steps of the viral replication cycle.
  • This review will provide some examples of the biological functions of ERvs. In particular, the role of ERVs in reproductive biology and in protecting the host against pathogenic retrovirus infections will be emphasized using enJSRVs/JSRV and the sheep as a model.

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  • (PMID = 19845636.001).
  • [ISSN] 1749-6632
  • [Journal-full-title] Annals of the New York Academy of Sciences
  • [ISO-abbreviation] Ann. N. Y. Acad. Sci.
  • [Language] ENG
  • [Grant] United States / NICHD NIH HHS / HD / R01 HD052745; United States / NICHD NIH HHS / HD / HD052745; United Kingdom / Wellcome Trust / /
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Other-IDs] NLM/ NIHMS634039; NLM/ PMC4199234
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18. Palmarini M, Datta S, Omid R, Murgia C, Fan H: The long terminal repeat of Jaagsiekte sheep retrovirus is preferentially active in differentiated epithelial cells of the lungs. J Virol; 2000 Jul;74(13):5776-87
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  • Jaagsiekte sheep retrovirus (JSRV) is the etiologic agent of a contagious bronchioloalveolar carcinoma of sheep known as sheep pulmonary adenomatosis (SPA; ovine pulmonary carcinoma).
  • JSRV is unique among retroviruses because it transforms the alveolar type II cells and the nonciliated bronchiolar cells (Clara cells) of the lungs; these cells are where JSRV is specifically expressed in both naturally and experimentally SPA-affected sheep.
  • By transient-transfection assays of 23 different cell lines with a reporter plasmid driven by the JSRV long terminal repeat (LTR), pJS21-luc, we found that the JSRV LTR is preferentially active in cell lines derived from type II pneumocytes and Clara cells (MLE-15 and mtCC1-2 mouse cell lines).

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  • (PMID = 10846056.001).
  • [ISSN] 0022-538X
  • [Journal-full-title] Journal of virology
  • [ISO-abbreviation] J. Virol.
  • [Language] ENG
  • [Grant] United States / NCI NIH HHS / CA / R01 CA082564; United States / NCI NIH HHS / CA / R01CA82564
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / DNA, Viral; 0 / NF-kappa B; 0 / Transcription Factors
  • [Other-IDs] NLM/ PMC112071
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19. Arnaud F, Varela M, Spencer TE, Palmarini M: Coevolution of endogenous betaretroviruses of sheep and their host. Cell Mol Life Sci; 2008 Nov;65(21):3422-32
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Jaagsiekte sheep retrovirus (JSRV) is a pathogenic exogenous retrovirus and the causative agent of ovine pulmonary adenocarcinoma.

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  • (PMID = 18818869.001).
  • [ISSN] 1420-9071
  • [Journal-full-title] Cellular and molecular life sciences : CMLS
  • [ISO-abbreviation] Cell. Mol. Life Sci.
  • [Language] ENG
  • [Grant] United States / NICHD NIH HHS / HD / R01 HD052745; United States / NICHD NIH HHS / HD / HD052745
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Review
  • [Publication-country] Switzerland
  • [Chemical-registry-number] 0 / Retroviridae Proteins, Oncogenic
  • [Number-of-references] 73
  • [Other-IDs] NLM/ NIHMS634040; NLM/ PMC4207369
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