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Characterization of aflatoxigenic and non-aflatoxigenic strains of Aspergillus section Flavi isolated from corn grains of different geographic origins in Brazil
Authors:Liliana de Oliveira Rocha  Gabriela Martins Reis  Raquel Braghini  Estela Kobashigawa  Jansen de Araújo  Benedito Corrêa
Affiliation:1.Department of Microbiology, Biomedical Institute II, Laboratory of Mycotoxins and Toxigenic Fungi,University of S?o Paulo,S?o Paulo,Brazil;2.Department of Food Engineering, School of Animal Science and Food Engineering, Laboratory of Microbiology and Food Micotoxicology,University of S?o Paulo,Pirassununga,Brazil;3.Department of Microbiology, Biomedical Institute II, Laboratory of Clinical and Molecular Virology,University of S?o Paulo,S?o Paulo,Brazil;4.Departamento de Microbiologia,Instituto de Ciências Biomédicas,S?o Paulo,Brazil
Abstract:Aflatoxins can cause great economic losses and serious risks to humans and animals health. The largest aflatoxin producers belong to Aspergillus section Flavi and can occur naturally in food commodities. Studies showed that molecular tools as well as the type of sclerotia produced by the strains could be helpful for identification of Aspergillus species and could be correlated with levels of toxin production. The purpose of this work was to characterize the genetic diversity using AFLP technique, the type of sclerotia and the ability of aflatoxin production by isolated strains from corn of different origins in Brazil, and to verify whether qPCR based on aflR and aflP genes is appropriate for estimating the level of aflatoxin production. All the 75 strains were classified as A. flavus and the AFLP technique showed a wide intraspecific variability within them. Regarding sclerotia production, 34% were classified as S and 66% as L type. Among the aflatoxin-producers, 52.8% produced aflatoxin B1, while 47.2% aflatoxins B1 and B2. Statistical analysis showed no correlation between sclerotia production and aflatoxigenicty, and no correlation between the phylogenetic clusters and aflatoxin production. Concerning the relative expression of aflR and aflP, Pearson’s correlation test demonstrated low positive correlation between the expression of the aflR and aflP genes and the production of AFB1 and AFB2, but showed high positive correlation between aflR and aflP expression. In contrast to the other reference strains, A. oryzae ATCC 7282 showed no amplification of aflR and aflP. The results highlight the need for detection of reliable and reproducible markers with a high positive correlation with aflatoxin production.
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