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Development of measles virus in vitro
Authors:T Nakai  F L Shand  A F Howatson
Affiliation:1. Ontario Cancer Institute, Toronto, Canada;2. Department of Medical Biophysics, University of Toronto, Toronto, Canada;1. School of Medicine, Western Sydney University, New South Wales;1. Center for Vaccine Sciences, icddr,b, Mohakhali, Dhaka 1212, Bangladesh;2. Department of Biochemistry and Molecular Biology, University of Dhaka, Dhaka, Bangladesh;1. University of Notre Dame, Department of Mathematics 255 Hurley, Notre Dame, IN 46556, United States of America;2. University of Kentucky, Department of Mathematics, 719 Patterson Office Tower, Lexington, KY 40506-0027, United States of America;1. Arbeitsgruppe für Gesundheitsökonomie und Gesundheitsmanagement, Fakultät für Gesundheitswissenschaften, Universität Bielefeld, Bielefeld, Deutschland;2. Abteilung für Gesundheitssystemanalyse und Gesundheitsökonomie, aQua-Institut, Göttingen, Deutschland;3. Nationales Centrum für Tumorerkrankungen (NCT) Heidelberg, Medizinische Onkologie, Universitätsklinikum Heidelberg, Heidelberg, Deutschland;1. University of Göttingen, Germany;2. University of Heidelberg, Germany
Abstract:The sequence of development of measles virus in cells cultivated in vitro was studied by electron microscopic techniques. The observations were correlated with virus growth measured by infectivity assay. Viral nucleoprotein tubules were first detected in the cytoplasm of infected cells, and shortly thereafter similar tubules were detected in the nucleus. In any one cell tubules were usually present either in the nucleus or in the cytoplasm, and rarely in both. No evidence suggesting that tubules migrated from one site to the other was obtained. At later stages in the infectious cycle, cytoplasmic tubules were extruded by a budding process at the cell surface, resulting in the formation of enveloped particles, interpreted as measles virions. Cytoplasmic tubule formation was associated with active budding and high yields of virus, whereas when intranuclear formation was predominant, little or no budding was detected and viral yields were low.The distribution of lengths of isolated nucleocapsids in negatively stained preparations showed a peak at 1.4-1.6 μ. When allowance was made for stretching of the nucleocapsid helix, this figure was reduced to 1.1 μ. The number of helical turns per nucleocapsid peaked sharply at a value of 204. On the assumption that the conformation of the measles nucleocapsid is similar to that of tobacco mosaic virus, the length and molecular weight of measles virus RNA were calculated and found to be 6.4μ and 6.2 × 106 daltons, respectively.
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