Monitoring Aspergillus flavus Genotypes in a Multi-Genotype Aflatoxin Biocontrol Product With Quantitative Pyrosequencing (original) (raw)

Polyphasic Assessment of Aflatoxin Production Potential in Selected Aspergilli

Toxins

This study investigated the aflatoxin production potentials of selected fungi using a polyphasic approach. Internally transcribed spacer region of the fungi was amplified using the polymerase chain reaction. Forty-five Aspergillus strains were further assessed for aflatoxin production using the conventional methods such as growth on yeast extract sucrose, β-cyclodextrin neutral red desiccated coconut agar (β-CNRDCA); expression of the aflatoxin regulatory genes and the use of both thin-layer chromatography (TLC) and high-performance liquid chromatography (HPLC). A large proportion (82.22%) of the isolates harbored the Nor-1 gene while 55.56%, 68.89%, and 80% possessed the ver-1, omt-A, and aflR genes, respectively. All 100% the isolates harbored the aflJ gene. Twenty-three isolates were positive for aflatoxin production based on the yeast extract sucrose medium (YES) test; ammonium vapor test (51%), yellow pigment production (75.5%), and β-CNRDCA tests; and blue/green fluorescence (...

Genetic diversity in Aspergillus flavus: association with aflatoxin production and morphology

Canadian Journal of Botany, 1993

Isolates of Aspergillus flavus belonging to at least 12 vegetative compatibility groups were characterized by aflatoxin production in vitro, morphology, and random amplified polymorphic DNAs. Aflatoxin B1 production differed significantly among vegetative compatibility groups; closely related isolates were similar intoxigenicity regardless of geographic origin. Cladistic analysis of DNA polymorphisms was consistent with vegetative compatibility data. A previously described dichotomy between S and L isolates of A. flavus based on morphology and physiology was strongly associated with both vegetative compatibility groups and DNA polymorphisms. All S isolates formed a single clade, apparently derived from the L group. Southern hybridizations of eight DNA amplification products showed that comigrating bands amplified by the same primer were always homologous within A. flavus but were not always homologous between A. flavus and closely related species. Results suggest that A. flavus is a...