EFS12- Book of abstracts - Contact
EFS12- Book of abstracts - Contact
EFS12- Book of abstracts - Contact
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SESSION 2: SECONDARY METABOLITES – BIOCHEMISTRY,<br />
BIOSYNTHESIS, FEED AND FOOD SAFETY<br />
P34 - A survey on pre- and post-harvest garlic bulbs:<br />
Fusarium proliferatum occurrence and fumonisins<br />
(B1, B2) accumulation<br />
S. Tonti 1 , M. Dal Prà 1 , S. Grandi 2 , P. Nipoti 2 , A. Prodi 2 , I. Alberti 1 , V. Cazzola 1<br />
1 INRAN - Istituto Nazionale per la Ricerca degli Alimenti e la Nutrizione, Via Ca’ Nova Zampieri 37, S.<br />
Giovanni Lupatoto (VR), Italy; 2 DipSA - Dipartimento di Scienze Agrarie, Alma Mater Studiorum,<br />
Università degli Studi di Bologna, Viale Fanin 40, 40127 Bologna, Italy.<br />
E-mail: i.alberti@ense.it<br />
Fusarium proliferatum is considered worldwide as an emerging pathogen <strong>of</strong> garlic.<br />
The presence <strong>of</strong> this fungus on plants during growing season it is hard to predict,<br />
but symptoms <strong>of</strong> the disease become clear after the harvest, during the<br />
conservation stage, when bulbs undergo a slow deterioration process. F.<br />
proliferatum is know to produce Fumonisins B1 and B2 on different vegetable<br />
matrices and Fumonisins contamination <strong>of</strong> garlic bulbs has been already reported<br />
in Germany.<br />
During year 2012, we performed a mycological screening in order to evaluate the<br />
pre- and post-harvest occurrence <strong>of</strong> F. proliferatum on asymptomatic garlic plants<br />
growing in the north-east <strong>of</strong> Italy. Fields were chosen for their different agronomic<br />
conditions: crop rotation, irrigation level and fertilizer types. Field samples<br />
consisted in whole plants eradicated with roots and bulbs at beginning <strong>of</strong> May.<br />
Post harvest samples consisted in unprocessed garlic bulbs, sampled prior to be<br />
cured. Fungal colonies morphologically resembling F. proliferatum were<br />
recovered from all the bulbs. The morphological identification was confirmed by<br />
Translation Elongation Factor 1-alpha (TEF) gene sequencing. All F. proliferatum<br />
strains were tested for their toxigenic potential by conventional PCR. A primer pair<br />
(FUM1P2-F and FUM1P2-R) designed on the sequence <strong>of</strong> FUM1 genes was<br />
used in this experiment. The effective presence <strong>of</strong> Fumonisins B1 and B2 on postharvest<br />
samples was evaluated by HPLC analysis.<br />
F. proliferatum was recovered at high frequencies from all the fields tested,<br />
suggesting that the presence <strong>of</strong> this fungus could be unrelated to the different<br />
agronomic practices. PCR and preliminary HPLC data demonstrate that the<br />
Fusarium dry rot population on garlic bulbs is potentially toxigenic and that<br />
Fumonisins B1 and B2 are always present at low levels on infected bulbs.<br />
Keywords: Fusarium proliferatum, garlic, mycotoxins detection<br />
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