molecular based strategy for rapid diagnosis of toxigenic Fusarium species associated to cereal grains from Argentina

• Published in: Fungal biology Vol. 114; no. 1; pp. 74 - 81
• Main Authors: Sampietro, D.A, Marín, P, Iglesias, J, Presello, D.A, Vattuone, M.A, Catalan, C.A.N, Gonzalez Jaen, M.T
• Format: Journal Article
• Language: English
• Published: Netherlands 2010
• Subjects: Argentina; DNA, Fungal - analysis; DNA, Fungal - isolation & purification; ear rot; Edible Grain - microbiology; Food Contamination; fumonisins; Fumonisins - metabolism; Fungal Proteins - genetics; Fungal Proteins - metabolism; fungi; Fusarium - classification; Fusarium - genetics; Fusarium - metabolism; Fusarium - pathogenicity; Fusarium proliferatum; genes; Gibberella fujikuroi var. subglutinans; Gibberella zeae; intergenic DNA; Mycological Typing Techniques; Mycotoxins - genetics; Mycotoxins - metabolism; nucleotide sequences; Peptide Elongation Factor 1 - genetics; Peptide Elongation Factor 1 - metabolism; physiology; polymerase chain reaction; Polymerase Chain Reaction - methods; prediction; ribosomal DNA; risk; small cereal grains; Species Specificity; subtropics; surveys; taxonomy; Time Factors; translation (genetics); trichothecenes; Trichothecenes - genetics; Trichothecenes - metabolism; Argentina
• ISSN: 1878-6146; 1878-6162
• DOI: 10.1016/j.mycres.2009.10.008

Fusarium species are worldwide causal agents of ear rot in cereals. Their toxigenic potential is a health risk for both humans and animals. In Argentina, most identification of these fungi has been based on morphological and cross-fertility criteria which are time consuming and require considerable expertise in Fusarium taxonomy and physiology. DNA based approaches have been reported as rapid, sensitive and specific alternatives to identify the main fumonisin and trichothecene-producing Fusarium species. In this work, we used PCR assays and the partial sequence of TEF1-α gene (Translation Elongation Factor-1α) to identify the fumonisin and trichothecene-producing species in Fusarium isolates from diverse regions of Argentina. The relative efficiency and reliability of those methods to improve mycotoxin risk prediction in this country were also assessed. Species-specific PCR assays were targeted toward multicopy IGS (Intergenic Spacer of rDNA units) and on the toxin biosynthetic genes FUM1 (fumonisins) and TRI13 and TRI7 genes (trichothecenes). PCR assays based on FUM1 gene and IGS sequences allowed detection and discrimination of the fumonisin producers Fusarium proliferatum and Fusarium verticillioides. Molecular identification of nonfumonisin producers from Gibberella fujikuroi species complex was possible after determination of TEF1-α gene sequences, which indicated the presence of Fusarium subglutinans, Fusarium andiyazi and Fusarium thapsinum. TEF-1α gene sequences also allowed discrimination of the different species of the Fusarium graminearum complex (F. graminearum sensu lato) as F. graminearum sensu stricto, Fusarium meridionale and Fusarium boothii. The last two species belonged to NIV chemotype and were detected for the first time in the subtropical region of Argentina while F. graminearum sensu stricto was DON producer only, which was also confirmed by specific PCR assays based on TRI137/TRI7 genes. Our results indicated that the PCR assays evaluated in this work are reliable diagnostic tools to detect the main toxigenic Fusarium species associated to cereal grains in Argentina. An extensive epidemiological survey based on the approach presented in this work is currently in progress to know the mycotoxigenic hazard of Fusarium species in cereal grains from the subtropical region of Argentina.