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Endophytic fungi from Vitis vinifera L. isolated in Canary Islands and ...

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Evaluation of the genetically modified corn resistance to fungal<strong>in</strong>fectionPopescu Sor<strong>in</strong>a*, Ioja-Boldura Oana Maria** Banat University of Agricultural Sciences <strong>and</strong> Veter<strong>in</strong>ary Medic<strong>in</strong>e Timisoara, Romania*Correspond<strong>in</strong>g author. Email: biotehnologii_usab@yahoo.comAbstract The genus Fusarium has a global distribution <strong>and</strong> many species<strong>in</strong> the genus are phytopathogenic <strong>fungi</strong> <strong>in</strong>fect<strong>in</strong>g a wide range of crop plants<strong>in</strong>clud<strong>in</strong>g cereals such as maize, wheat, oat <strong>and</strong> barley. Insect pests of cornare often <strong>in</strong>volved <strong>in</strong> the disease cycles of ear rot <strong>and</strong> stalk rot diseases. TheEuropean corn borer is particularly well known for its <strong>in</strong>volvement <strong>in</strong> thesediseases. Bt corn is a variant of maize, genetically modified to express thebacterial Bt tox<strong>in</strong>, which protect the plants aga<strong>in</strong>st this pest, thereforereduc<strong>in</strong>g the <strong>in</strong>tensity of Fusarium contam<strong>in</strong>ation. PCR based methods weresuccessfully applied <strong>in</strong> the screen<strong>in</strong>g for identification of contam<strong>in</strong>ation withpathogenic <strong>fungi</strong> for the corn samples. 14 corn samples, GM <strong>and</strong>conventional were subjected to PCR screen<strong>in</strong>g <strong>in</strong> order to detect thepresence of three Fusarium species. The presence of Fusariun proliferatumwas not detected <strong>in</strong> the GM corn samples. All three tested Fusarium species,were found <strong>in</strong> the analyzed samples, <strong>in</strong> average conventional corn be<strong>in</strong>g themost affected.Key wordsBt corn, contam<strong>in</strong>ation,Fusarium ssp., detection,PCRFusarium stra<strong>in</strong> identification <strong>in</strong> complex feeds <strong>from</strong> RomanianmarketIoja-Boldura Oana Maria 1 , Popescu Sor<strong>in</strong>a 11 Banat University of Agricultural Sciences <strong>and</strong> Veter<strong>in</strong>ary Medic<strong>in</strong>e Timisoara*Correspond<strong>in</strong>g author. Email: biotehnologii_usab@yahoo.comAbstract Fusarium contam<strong>in</strong>ation is a major agricultural problem asquality <strong>and</strong> yield can be reduced, but more importantly many species <strong>in</strong> thegenus produce mycotox<strong>in</strong>s responsible for serious diseases <strong>in</strong> humans <strong>and</strong>farm animals. The most common mycotox<strong>in</strong>e <strong>in</strong> cereals is deoxynivalenol(DON) produced by certa<strong>in</strong> isolates of Fusarium spp., be<strong>in</strong>g prevalentworldwide <strong>in</strong> crops used for food <strong>and</strong> feed production. Identification ofFusarium species is critical to predict the potential mycotoxigenic risk of thecereals, therefore the development of an accurate <strong>and</strong> complementarymethod which permits a rapid, sensitive <strong>and</strong> reliable specific diagnosis ofFusarium species, is necessary. DNA based approaches applied <strong>in</strong> this studyhave been already reported as rapid, sensitive <strong>and</strong> specific alternatives toidentify the ma<strong>in</strong> trichothecene-produc<strong>in</strong>g Fusarium species. The biologicalmaterial consisted of eight samples of commercial feeds were all positive forFusarium species <strong>and</strong> therefore be<strong>in</strong>g suitable for further identification ofthose pathogenic organisms. In addition two of tox<strong>in</strong>s biosynthetic genes werealso detected. Therefore, this method proved to be suitable <strong>in</strong> screen<strong>in</strong>g offorage samples, <strong>in</strong> order to detect their contam<strong>in</strong>ation.Key wordsFusariumssp.,mycotox<strong>in</strong>es, feed products,screen<strong>in</strong>g, PCR

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