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Background and
Objectives:
Aster yellows describe a disease
caused by phytoplasma, carried by leafhoppers and transmitted to plants
as these insects feed. In the last few years, this disease severely
affected carrot crops in Manitoba. Due to the complex nature of the
insect- phytoplasma- plant-environment interactions, aster yellows
disease management and control in carrots require a multidisciplinary
approach, including a fast and accurate detection system.
The main objectives of this
project included:
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The use of molecular
techniques, namely PCR, for a more accurate determination of aster
yellows incidence in selected carrot fields in Manitoba.
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Using such technology on
species other than carrots for possible identification of alternate
sources of inoculum.
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Using molecular techniques,
namely RFLPs, for characterization of phytoplasmas isolated from both
carrots and leafhopper vectors.
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Using such knowledge towards
investigating leafhopper population dynamics in the field.
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Suggesting additional control
strategies to combat aster yellows phytoplasma in carrots, based on
the generated knowledge.
Procedure and Project
Activities:
Five carrot fields in the
Portage la Prairie area were selected to determine aster yellows disease
incidence in Manitoba in both 2001 and 2002. During each visit, fields
were scouted for aster yellows symptoms on carrot and other plant
species, and both healthy plants and those suspected to be infected with
aster yellows were collected for molecular detection of the pathogen.
At the same time, insect populations were monitored (over 1,000 and
1,500 leafhoppers for the five fields in 2001 and 2002, respectively)
and molecular techniques were used to detect and characterize the aster
yellows phytoplasma they harbour.
Results and Discussion:
In this project, many
accomplishments could be enumerated:
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Accuracy of visual symptom
determination was estimated for both healthy- and diseased-looking
samples.
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We were able to adapt PCR
techniques to our carrot plants and to leafhoppers, and phytoplasma
detection was successful in both types of tissues using slightly
different protocols.
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Phytoplasma found in Manitoba in this study were classified either in
sub-group I-A or I-B, same as those found in Alberta. Multiple
infection with phytoplasma from both sub-groups were found in both
carrots and leafhoppers.
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Aster yellows phytoplasmas
were found in other plant species, which can represent a source of
inoculum.
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The risk of aster yellows
phytoplasma is higher during the early season, rather than middle and
late season, based on the percent infection of leafhoppers.
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Given that risk of infection
is higher early in the season, protective measures should be applied
both early and later in the season. Protective measures should be
applied and decisions should be made on the basis of presence of
leafhoppers during the early part of the growing season (May, June).
This is contrary to current management practices relying exclusively
on the Aster Yellows Index (AYI) as a decision making tool.
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The use of AYI might be
subject to some error given that it is derived from populations of
leafhoppers from Wisconsin. The subsequent leafhoppers that arrive in
Manitoba have had ample time to pick up more inoculum, hence may have
a higher rate of infectivity. This is confirmed by this study in that
few leafhoppers are present early in the season yet the infectivity
rate is much higher than typical AYI estimates.
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Later season populations
should be monitored and the AYI can remain as a decision making tool.
The reason it remains effective is that Manitoba populations of
leafhoppers are less infective as a whole, later in the season, and
the AYI estimate may more closely correlate with Wisconsin estimates.
This has the added benefit or reducing or limiting pesticide use
later in the season.
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