Literature DB >> 4863047

Some conditions affecting the intracellular arrangement and concentration of tobacco mosaic virus particles in local lesions.

M Weintraub, H W Ragetli, V T John.   

Abstract

Tobacco mosaic virus particles were found in small packets and in small numbers, with the electron microscope, in necrotic leaf cells of Nicotiana glutinosa when the samples were fixed in glutaraldehyde and postfixed in OsO(4), and the sections were stained with heavy metals. The numbers and size of the virus packets were increased greatly when the leaves were detached from the plant after inoculation Assay of concentration showed that detachment resulted in a 30-fold increase of virus. A similar increase in the number of virus particles detected by electron microscopy was produced by keeping inoculated plants at an air temperature of 26 degrees C. A still greater increase in concentration was effected by incubating detached inoculated leaves at 26 degrees C. Moreover the arrangement of virus particles in these cells resembled that of a systemic virus infection. Cells in local lesions of Chenopodium amaranticolor contained large numbers of virus particles both as packets and in the loose arrangement characteristic of systemic infection. Neither the number of particles nor their arrangement was affected in this host by detaching the leaf or by changing the air temperature. It is suggested that there may be two types of localized virus infections, one of which produces virus in low concentration and is amenable to changes in virus concentration and arrangement as a result of environmental manipulation.

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Year:  1967        PMID: 4863047      PMCID: PMC2107107          DOI: 10.1083/jcb.35.1.183

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  19 in total

1.  IMMUNO-OSMOPHORESIS, A RAPID AND SENSITIVE METHOD FOR EVALUATING VIRUSES.

Authors:  H W RAGETLI; M WEINTRAUB
Journal:  Science       Date:  1964-05-22       Impact factor: 47.728

2.  Intermediary products formed during tobacoco mosaic virus reproduction.

Authors:  H ZECH
Journal:  Virology       Date:  1960-06       Impact factor: 3.616

3.  Visualization of tobacco mosaic virus in local lesions of Datura stramonium.

Authors:  T W Carroll; T A Shalla
Journal:  Phytopathology       Date:  1965-08       Impact factor: 4.025

4.  Electron microscopy of tobacco mosaic virus in leaves of Nicotiana glutinosa.

Authors:  R G Milne
Journal:  Virology       Date:  1966-04       Impact factor: 3.616

5.  Electron miroscopy of cytoplasmic inclusions in cells infected with rod-shaped viruses.

Authors:  J R Edwardson
Journal:  Am J Bot       Date:  1966-04       Impact factor: 3.844

6.  Fine structure of inclusions and organelles in Vicia faba infected with bean yellow mosaic virus.

Authors:  M Weintraub; H W Ragetli
Journal:  Virology       Date:  1966-02       Impact factor: 3.616

7.  Simple methods for "staining with lead" at high pH in electron microscopy.

Authors:  M J KARNOVSKY
Journal:  J Biophys Biochem Cytol       Date:  1961-12

8.  Improvements in epoxy resin embedding methods.

Authors:  J H LUFT
Journal:  J Biophys Biochem Cytol       Date:  1961-02

9.  A simplified method of staining thin sections of biolgical material with lead hydroxide for electron microscopy.

Authors:  A J DALTON; R F ZEIGEL
Journal:  J Biophys Biochem Cytol       Date:  1960-04

10.  Cytochemistry and electron microscopy. The preservation of cellular ultrastructure and enzymatic activity by aldehyde fixation.

Authors:  D D SABATINI; K BENSCH; R J BARRNETT
Journal:  J Cell Biol       Date:  1963-04       Impact factor: 10.539

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  2 in total

Review 1.  Fungal viruses.

Authors:  P A Lemke; C H Nash
Journal:  Bacteriol Rev       Date:  1974-03

2.  Intracellular characterization of bean yellow mosaic virus-induced inclusions by differential enzyme digestion.

Authors:  M Weintraub; H W Ragetli
Journal:  J Cell Biol       Date:  1968-08       Impact factor: 10.539

  2 in total

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