Isolation and characterization of a 14500 molecular weight protein from brains and tissue cultures persistently infected with Borna disease virus

Institut für Virologie, Freie Universität Berlin and 1 Robert Koch-Institut des Bundesgesundheitsamtes, Nordufer 20, 1000 Berlin 65, F.R.G. A protein with an apparent molecular weight of 14 500 (14.5K) was extractable from homogenates of Borna disease virus-infected brains and tissue cultures using...

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Veröffentlicht in:Journal of general virology 1985-11, Vol.66 (11), p.2479-2484
Hauptverfasser: Schadler, R, Diringer, H, Ludwig, H
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container_title Journal of general virology
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creator Schadler, R
Diringer, H
Ludwig, H
description Institut für Virologie, Freie Universität Berlin and 1 Robert Koch-Institut des Bundesgesundheitsamtes, Nordufer 20, 1000 Berlin 65, F.R.G. A protein with an apparent molecular weight of 14 500 (14.5K) was extractable from homogenates of Borna disease virus-infected brains and tissue cultures using high concentrations of detergent and salt and by differential centrifugation procedures. The protein, present in an aggregated form, was remarkably resistant to proteinase K. Specific antibodies prepared in the homologous system (rat) recognized the 14.5K protein from various sources (infected brain of rat, mouse or chicken, and tissue cultures), but did not neutralize infectivity nor stain Borna disease virus-specific antigens from in vitro or in vivo preparations. Post-infection immune sera from different animal species did not detect the protein. This 14.5K protein was infection-specific but not disease-specific, and is inferred to be part of an internal virion component. Keywords: BD virus, 14.5K protein, persistent infection Received 8 July 1985; accepted 9 August 1985.
doi_str_mv 10.1099/0022-1317-66-11-2479
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A protein with an apparent molecular weight of 14 500 (14.5K) was extractable from homogenates of Borna disease virus-infected brains and tissue cultures using high concentrations of detergent and salt and by differential centrifugation procedures. The protein, present in an aggregated form, was remarkably resistant to proteinase K. Specific antibodies prepared in the homologous system (rat) recognized the 14.5K protein from various sources (infected brain of rat, mouse or chicken, and tissue cultures), but did not neutralize infectivity nor stain Borna disease virus-specific antigens from in vitro or in vivo preparations. Post-infection immune sera from different animal species did not detect the protein. This 14.5K protein was infection-specific but not disease-specific, and is inferred to be part of an internal virion component. 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A protein with an apparent molecular weight of 14 500 (14.5K) was extractable from homogenates of Borna disease virus-infected brains and tissue cultures using high concentrations of detergent and salt and by differential centrifugation procedures. The protein, present in an aggregated form, was remarkably resistant to proteinase K. Specific antibodies prepared in the homologous system (rat) recognized the 14.5K protein from various sources (infected brain of rat, mouse or chicken, and tissue cultures), but did not neutralize infectivity nor stain Borna disease virus-specific antigens from in vitro or in vivo preparations. Post-infection immune sera from different animal species did not detect the protein. This 14.5K protein was infection-specific but not disease-specific, and is inferred to be part of an internal virion component. 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A protein with an apparent molecular weight of 14 500 (14.5K) was extractable from homogenates of Borna disease virus-infected brains and tissue cultures using high concentrations of detergent and salt and by differential centrifugation procedures. The protein, present in an aggregated form, was remarkably resistant to proteinase K. Specific antibodies prepared in the homologous system (rat) recognized the 14.5K protein from various sources (infected brain of rat, mouse or chicken, and tissue cultures), but did not neutralize infectivity nor stain Borna disease virus-specific antigens from in vitro or in vivo preparations. Post-infection immune sera from different animal species did not detect the protein. This 14.5K protein was infection-specific but not disease-specific, and is inferred to be part of an internal virion component. Keywords: BD virus, 14.5K protein, persistent infection Received 8 July 1985; accepted 9 August 1985.</abstract><cop>England</cop><pub>Soc General Microbiol</pub><pmid>3932595</pmid><doi>10.1099/0022-1317-66-11-2479</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Microbiology Society; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects animal proteins
Animals
Borna Disease - immunology
Borna Disease - microbiology
Borna disease virus
Brain - microbiology
Brain Chemistry
Cells, Cultured
characterization
Chickens
Horse Diseases - microbiology
Horses
Humans
Immune Sera - immunology
isolation
Mice
Mice, Inbred BALB C
Molecular Weight
Rabbits
Rats
Rats, Inbred Strains
Viral Proteins - analysis
Viral Proteins - immunology
Viral Proteins - isolation & purification
Viruses, Unclassified
title Isolation and characterization of a 14500 molecular weight protein from brains and tissue cultures persistently infected with Borna disease virus
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