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EFS12- Book of abstracts - Contact

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SESSION 2: SECONDARY METABOLITES – BIOCHEMISTRY,<br />

BIOSYNTHESIS, FEED AND FOOD SAFETY<br />

P32 - Chemotype diversity and pathogenicity <strong>of</strong><br />

Fusarium graminearum species complex originating<br />

from Serbian cereals grain<br />

S. Stanković 1 , A. Obradović 1 , J. Lević 1 , G. Vuković 2 , V. Krnjaja 3<br />

1 Maize Research Institute, Zemun Polje, Belgrade-Zemun, S. Bajića 1, 11185 Belgrade, Republic <strong>of</strong><br />

Serbia; 2 Institute <strong>of</strong> Public Health, Boulevard <strong>of</strong> Despot Stefan 54a, 11000 Belgrade, Republic <strong>of</strong><br />

Serbia 3 Institute for Animal Husbandry, Autoput 16, 11080, Belgrade-Zemun, Republic <strong>of</strong> Serbia<br />

E-mail: sstojkov@mrizp.rs<br />

Members <strong>of</strong> the Fusarium graminearum species complex are important plant<br />

pathogens and belong to one <strong>of</strong> at least thirteen phylogenetically distinct species.<br />

These species cause Fusarium head blight or scab <strong>of</strong> wheat, barley and rice, and<br />

ear rot <strong>of</strong> maize. In addition to quantitative yield losses, harvested grain sustains<br />

qualitative problems <strong>of</strong> contamination with mycotoxins such as nivalenol (NIV),<br />

deoxynivalenol (DON) and its acetylated forms (3AcDON and 15AcDON). In this<br />

study, pathogenicity, trichothecene chemotype and toxin potential <strong>of</strong> fifty F.<br />

graminearum sensu lato isolates collected from wheat, maize and barley kernels<br />

in 47 localities in Serbia was examined. Chemotyping <strong>of</strong> investigated isolates was<br />

done by LC-MS analyses <strong>of</strong> extracts from cultures inoculated onto maize and<br />

wheat kernels. Mycotoxin production potential <strong>of</strong> isolates was analyzed by ELISA<br />

(enzyme–linked immunosorbent assays). The assays were carried out according<br />

to the manufacturer’s instructions. (Tecna S.r.l., Italy). Pathogenicity <strong>of</strong> the<br />

investigated isolates was tested in vivo (field conditions) and in vitro (laboratory<br />

conditions). In the field test, pathogenicity was assessed after silk channel<br />

inoculation with a conidial suspension <strong>of</strong> each investigated isolates prepared with<br />

siglespored cultures. The primary ears <strong>of</strong> the ten plants per replication were<br />

inoculated at 5 days post-silk emergence with inoculum prepared as previously<br />

described Raid et al. (1992). In vitro, detached leaf assays involving artificial<br />

inoculation <strong>of</strong> wounded wheat leaves <strong>of</strong> 2-week-old seedlings (Imathiu et al,<br />

2009). Three isolate out <strong>of</strong> fifty belonged to 3AcDON chemotype, and all the<br />

others to 15AcDON chemotype. On average, 3AcDON isolates produced the<br />

highest, but statistically no significant, concentration <strong>of</strong> trichothecene. No<br />

significant positive correlation was found between the isolates pathogenicity and<br />

toxin production in both, in vivo (r = 0.22 ns ) and in vitro (r = 0,32 ns ) test.<br />

Keywords: Fusarium, deoxynivalenol, chemotype, pathogenicity<br />

124

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