Frog Virus 3 Morphogenesis: Effect of Temperature and Metabolic Inhibitors

Groupe de Recherches de l'I.N.S.E.R.M. sur la Pathogénie des Infections Virales et Laboratoire de Virologie de la Faculté de Médecine, Université Louis Pasteur, 3, rue Koeberlé 67000 Strasbourg, France The different stages of frog virus 3 (FV 3) morphogenesis have been investigated in chick emb...

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Veröffentlicht in:Journal of general virology 1977-10, Vol.37 (1), p.39-52
Hauptverfasser: Tripier, Francoise, Braunwald, Jacqueline, Markovic, Lj, Kirn, A
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container_end_page 52
container_issue 1
container_start_page 39
container_title Journal of general virology
container_volume 37
creator Tripier, Francoise
Braunwald, Jacqueline
Markovic, Lj
Kirn, A
description Groupe de Recherches de l'I.N.S.E.R.M. sur la Pathogénie des Infections Virales et Laboratoire de Virologie de la Faculté de Médecine, Université Louis Pasteur, 3, rue Koeberlé 67000 Strasbourg, France The different stages of frog virus 3 (FV 3) morphogenesis have been investigated in chick embryo fibroblasts infected at an optimal temperature for virus growth (29 °C). The metabolic requirements for morphogenesis were determined by adding inhibitors of macromolecular synthesis at different periods in the virus growth cycle. The effect of a non-permissive temperature for FV 3 replication (37 °C) was also studied in shift up experiments. The following results were obtained: (1) when DNA replication was inhibited, neither immature nor mature virus particles appeared; (2) continuous protein synthesis was required for every stage of virus morphogenesis. However, the assembly of virions into paracrystalline arrays seemed to be a passive phenomenon. (3) Continuous mRNA transcription was not necessary for assembly of capsid constituents, although most of these capsids appeared empty; there was also a striking increase in the number of aberrant virus structures. (4) If infected cells were shifted to a non-permissive temperature, virus maturation was completely inhibited. * Present address: Institute of Microbiology, Faculty of Medicine, 11000 Beograd, Dr. Subotica 1, Yugoslavia. Received 10 January 1977;
doi_str_mv 10.1099/0022-1317-37-1-39
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The metabolic requirements for morphogenesis were determined by adding inhibitors of macromolecular synthesis at different periods in the virus growth cycle. The effect of a non-permissive temperature for FV 3 replication (37 °C) was also studied in shift up experiments. The following results were obtained: (1) when DNA replication was inhibited, neither immature nor mature virus particles appeared; (2) continuous protein synthesis was required for every stage of virus morphogenesis. However, the assembly of virions into paracrystalline arrays seemed to be a passive phenomenon. (3) Continuous mRNA transcription was not necessary for assembly of capsid constituents, although most of these capsids appeared empty; there was also a striking increase in the number of aberrant virus structures. (4) If infected cells were shifted to a non-permissive temperature, virus maturation was completely inhibited. * Present address: Institute of Microbiology, Faculty of Medicine, 11000 Beograd, Dr. Subotica 1, Yugoslavia. 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The metabolic requirements for morphogenesis were determined by adding inhibitors of macromolecular synthesis at different periods in the virus growth cycle. The effect of a non-permissive temperature for FV 3 replication (37 °C) was also studied in shift up experiments. The following results were obtained: (1) when DNA replication was inhibited, neither immature nor mature virus particles appeared; (2) continuous protein synthesis was required for every stage of virus morphogenesis. However, the assembly of virions into paracrystalline arrays seemed to be a passive phenomenon. (3) Continuous mRNA transcription was not necessary for assembly of capsid constituents, although most of these capsids appeared empty; there was also a striking increase in the number of aberrant virus structures. (4) If infected cells were shifted to a non-permissive temperature, virus maturation was completely inhibited. * Present address: Institute of Microbiology, Faculty of Medicine, 11000 Beograd, Dr. Subotica 1, Yugoslavia. 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source MEDLINE; Microbiology Society; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects Animals
Chick Embryo
Culture Techniques
Cycloheximide - pharmacology
Cytarabine - pharmacology
Dactinomycin - pharmacology
DNA Replication - drug effects
DNA, Viral - biosynthesis
Iridoviridae - drug effects
Iridoviridae - growth & development
Iridoviridae - metabolism
Morphogenesis - drug effects
Temperature
Viral Proteins - biosynthesis
Virus Replication - drug effects
title Frog Virus 3 Morphogenesis: Effect of Temperature and Metabolic Inhibitors
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