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Journal ArticleDOI

Detection of potato leafroll and potato mop-top viruses by immunosorbent electron microscopy

I. M. Roberts, +1 more
- 01 Dec 1979 - 
- Vol. 93, Iss: 3, pp 289-297
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TLDR
Attachment of virus particles to antiserum-coated electron microscope grids (immunosorbent electron microscopy) provided a test that was at least a thousand times more sensitive for detecting potato leafroll (PLRV) and potato mop-top (PMTV) viruses.
Abstract
SUMMARY Attachment of virus particles to antiserum-coated electron microscope grids (immunosorbent electron microscopy) provided a test that was at least a thousand times more sensitive than conventional electron microscopy for detecting potato leafroll (PLRV) and potato mop-top (PMTV) viruses. The identity of the attached virus particles was confirmed by exposing them to additional virus antibody, which coated the particles. PLRV particles (up to 50/μm2 of grid area) were detected in extracts of infected potato leaves and tubers, infected Physalis floridana leaves, and single virus-carrying aphids. On average, Myzus persicae yielded 10–30 times more PLRV particles than did Macrosiphum euphorbiae. PMTV particles (up to 10/μm2 of grid area) were detected in extracts of inoculated tobacco leaves, and of infected Arran Pilot potato tubers with symptoms of primary infection. Particles from tobacco leaves were of two predominant lengths, about 125 nm or about 290 nm, and fewer particles of other lengths were found than in previous work, in which partially purified or purified preparations of virus particles were examined, using grids not coated with antiserum.

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Citations
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Geminivirus coat protein gene replacement alters insect specificity

TL;DR: Results show that the specificity of leafhopper transmission from insect to plant resides with the coat protein, which is typical of ACMV infection.
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Immunosorbent assays in plant pathology

TL;DR: This review assesses the current state of knowledge of immunosorbent assays, in particular ELISA, concentrating on those variable aspects of the technique that are likely to affect its performance in the qualitative and quantitative detection of plant pathogens.
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The coat protein of beet curly top virus is essential for infectivity.

TL;DR: It is concluded that the coat protein of BCTV is essential for spread of the virus.
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Mutational analysis of complementary-sense genes of African cassava mosaic virus DNA A.

TL;DR: Typical geminate virus particles were observed in extracts of plants infected with ORF AC3 mutants indicating that this gene is not essential for coat protein synthesis or virus assembly but possibly acts by modulating virus levels in infected tissues.
Journal ArticleDOI

Production of Monoclonal Antibodies to African Cassava Mosaic Virus and Differences in Their Reactivities with Other Whitefly-transmitted Geminiviruses

TL;DR: Results of competitive binding tests, when combined with the patterns of reaction of individual MAbs with different viruses, indicated that the MAbs were specific for nine distinct epitopes, suggesting that the epitopes detected by these MAbs may be important for transmission by B. tabaci.
References
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Journal ArticleDOI

The lattice spacing of crystalline catalase as an internal standard of length in electron microscopy

TL;DR: The preparation of crystals of bovine liver catalase, and their use as an internal standard of length in electron microscopy, are described and a critical appraisal of all available data suggests a figure of 172±4 A for the principalCatalase lattice spacing.
Journal ArticleDOI

Quantitative assay for plant viruses using serologically specific electron microscopy

TL;DR: The log of the number of TMV particles attached to grids serologically specific for TMV decreased linearly with dilution of virus extract, and the method simplified the collection and analysis of virus particles.
Journal ArticleDOI

Enzyme-assisted Purification of two Phloem-limited Plant Viruses: Tobacco Necrotic Dwarf and Potato Leafroll

TL;DR: Tobacco necrotic dwarf (TNDV) and potato leafroll (PLRV), viruses which are normally phloem-limited and are transmitted by aphids in the persistent manner, were successfully purified using Driselase, an enzyme that macerates plant tissue.
Journal ArticleDOI

Assay for viruses and mycoplasmas using serologically specific electron microscopy.

K. S. Derrick, +1 more
- 01 Jan 1976 - 
TL;DR: The dilution of antiserum used to further developed as a diagnostic technique for plant viruses, prepare SSEM grids did not have a significant effect on the technique, and was shown to apply to a variety of plant number of virus particles attached, except at extremely high viruses and to the corn stunt mycoplasma (CSM).
Journal ArticleDOI

Host range, properties and purification of Raspberry bushy dwarf virus.

TL;DR: RBDV caused systemic symptoms in some species of Amaranthaceae, Chenopodiaceae and Cucurbitaceae, and necrotic local lesions in some Leguminosae, and did not induce bushy dwarf disease when returned to Lloyd George raspberry.
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