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Plant virus inhibitors from marine algae Pardee, Keith
Abstract
This study was the first to evaluate new world algal species for compounds with potential for plant virus chemotherapy. Methanolic extracts from 30 species of marine algae were assayed for antiviral activity against potato virus X (PVX) in local lesion assays using Chenopodium quinoa L. as host. Extracts from six algal species (Fucus gardneri Silva, Alaria nana Schrader, Ralfsia sp. (Berkley), Codium fragile (Suringar) Hariot, Fragilaria oceanica Cleve, Egregia menziesii (Turner) J.E. Areschoug) inhibited PVX infectivity by more than 80%, with a disproportionate number of these extracts coming from the phylum Heterokontophyta. Of the six most active extracts, it is the first time that Fucus gardneri, Ralfsia sp. and Fragilaria oceanica have been reported as sources of antiviral agents. Antiviral activity from the most potent extract, F. gardneri, was selected for phytochemical analysis. Fractionation of the crude extract resulted in the isolation and identification of the polysaccharide alginate as a source of bioactivity. Alginate inhibited potato virus X infectivity by 95%, and preliminary transmission electron microscopy indicates that the mode of action may be related to aggregation of virus particles. Bioactivity in a second fraction was the result of phenolic and amino-based compounds that have yet to be positively identified.
Item Metadata
Title |
Plant virus inhibitors from marine algae
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Creator | |
Publisher |
University of British Columbia
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Date Issued |
2002
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Description |
This study was the first to evaluate new world algal species for compounds with
potential for plant virus chemotherapy. Methanolic extracts from 30 species of
marine algae were assayed for antiviral activity against potato virus X (PVX) in
local lesion assays using Chenopodium quinoa L. as host. Extracts from six
algal species (Fucus gardneri Silva, Alaria nana Schrader, Ralfsia sp. (Berkley),
Codium fragile (Suringar) Hariot, Fragilaria oceanica Cleve, Egregia
menziesii (Turner) J.E. Areschoug) inhibited PVX infectivity by more than
80%, with a disproportionate number of these extracts coming from the
phylum Heterokontophyta. Of the six most active extracts, it is the first time
that Fucus gardneri, Ralfsia sp. and Fragilaria oceanica have been reported
as sources of antiviral agents. Antiviral activity from the most potent extract, F.
gardneri, was selected for phytochemical analysis. Fractionation of the crude
extract resulted in the isolation and identification of the polysaccharide alginate
as a source of bioactivity. Alginate inhibited potato virus X infectivity by 95%,
and preliminary transmission electron microscopy indicates that the mode of
action may be related to aggregation of virus particles. Bioactivity in a second
fraction was the result of phenolic and amino-based compounds that have yet
to be positively identified.
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Extent |
5596163 bytes
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Genre | |
Type | |
File Format |
application/pdf
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Language |
eng
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Date Available |
2009-08-13
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Provider |
Vancouver : University of British Columbia Library
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Rights |
For non-commercial purposes only, such as research, private study and education. Additional conditions apply, see Terms of Use https://open.library.ubc.ca/terms_of_use.
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DOI |
10.14288/1.0090269
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URI | |
Degree | |
Program | |
Affiliation | |
Degree Grantor |
University of British Columbia
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Graduation Date |
2002-05
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Campus | |
Scholarly Level |
Graduate
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Aggregated Source Repository |
DSpace
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Item Media
Item Citations and Data
Rights
For non-commercial purposes only, such as research, private study and education. Additional conditions apply, see Terms of Use https://open.library.ubc.ca/terms_of_use.