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International Congress BIOLOGICAL PRODUCTS - Gruppo di ...

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25<br />

EFFICACY EVALUATION OF <strong>BIOLOGICAL</strong> CONTROL AGENTS AGAINST<br />

PLASMOPARA VITICOLA<br />

Ilaria Pertot, Federica De Luca, Antonella Vecchione, Luca Zulini<br />

Istituto Agrario <strong>di</strong> San Michele all’A<strong>di</strong>ge, via E. Mach 1, S. Michele all’A<strong>di</strong>ge (TN)<br />

ilaria.pertot@ismaa.it<br />

Keywords<br />

downy mildew, Plasmopara viticola, biological control agents, organic agriculture.<br />

Introduction<br />

Downy mildew causal agent, Plasmopara viticola (Berk. et Curt.) Berl. et De Toni, is one of the most important<br />

grapevine pathogens, causing great losses if no protective treatments are applied (Kortekamp, 1997).<br />

Nowadays consumer and farmer are much more concerned about food, health and environment safety (Butt,<br />

2001). The con<strong>di</strong>tions for using copper will be restricted by European Union by fixing a ceiling on use expressed<br />

in terms of kilograms of copper per hectare per year in organic agriculture. Antagonist microorganisms could be<br />

a possible alternative to copper in downy mildew controlling. Epidemiological characteristics of downy mildew<br />

probably would not allow a complete field control based on a single biocontrol agent (BCA). A possible solution<br />

for improving efficacy of BCA could be the integration of several micro-organisms with <strong>di</strong>fferent action<br />

mechanisms on specific stages of <strong>di</strong>sease: i) during oospore overwintering and germination, for primary<br />

inoculum reduction ii) and during sporangia germination for protection against secondary infections.<br />

Materials and methods<br />

Micro-organisms were isolated from grapevine leaf material and rhizosphere of 18 <strong>di</strong>fferent vineyards located in<br />

the north –east of Italy. Vineyards were abandoned and chemically untreated for at least three years. Microorganisms<br />

were isolated on potato dextrose agar, malt agar and nutrient sucrose agar and grown at 20°C. Several<br />

isolation methods were used: inocula were based on leaf washing water, necrotic leaf portions grounded in sterile<br />

water with mortar and pestle, necrotic leaf pieces, infected leaf <strong>di</strong>sh maintained in contact with naturally<br />

degraded leaf material and root surface material. For each kind of material used, all morphologically <strong>di</strong>fferent<br />

colonies of fungi and bacteria were collected. A sample of 46 isolates was evaluated for sporangia germination<br />

and infection inhibition activity. A sample of 33 isolates was evaluated for overwintering oospores inhibition<br />

activity.<br />

The evaluation methods used were:<br />

i) oospore germination inhibition, based on a mo<strong>di</strong>fied floating leaf <strong>di</strong>sk method (Hill);<br />

ii) inhibition of sporangia germination, based on reduction percentage of sporangia germination in a 1:1<br />

water solution of the isolate culture broth and P. viticola sporangia;<br />

iii) infection inhibition, based on the reduction of the number of sporangiophore developed on isolate<br />

culture broth treated leaves.<br />

Results and <strong>di</strong>scussion<br />

Several micro-organisms have induced a partial inhibition of sporangia germination (tab. 1), but the complete<br />

control of infection on leaf can be achieved with only few of them.<br />

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