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@ARTICLE{TreeBASE2Ref15524, author = {David M. Geiser and Joe W. Dorner and Bruce W. Horn and John W. Taylor}, title = {The phylogenetics of mycotoxin and sclerotium production in Aspergillus flavus and Aspergillus oryzae.}, year = {2000}, keywords = {aflatoxin; Aspergillus section Flavi; cyclopiazonic acid; cryptic species; gene genealogies}, doi = {10.1006/fgbi.2000.1215}, url = {}, pmid = {}, journal = {Fungal Genetics and Biology}, volume = {31}, number = {3}, pages = {169--179}, abstract = {Aspergillus flavus is a common filamentous fungus that produces aflatoxins and presents a major threat to agriculture and human health. Previous phylogenetic studies of A. flavus have shown that it consists of two subgroups, called groups I and II, and morphological studies indicated that it consists of two morphological groups based on sclerotium size, called S and L. The industrially important non-aflatoxin producing fungus A. oryzae is nested within group I. Three different gene regions, including part of a gene involved involved in aflatoxin biosynthesis (omt12), were sequenced in 33 S and L strains of A. flavus collected from various regions around the world, along with three isolates of A. oryzae, and two isolates of A. parasiticus that were used as outgroups. The production of B and G aflatoxins and cyclopiazonic acid was analyzed in the A. flavus isolates, and each isolate was identified as S or L based on sclerotium size. Phylogenetic analysis of all three genes confirmed the inference that group I and group II represent a deep divergence within A. flavus. Most group I strains produced B aflatoxins to some degree, and none produced G aflatoxins. Four out of six group II strains produced both B and G aflatoxins. All group II isolates were of the S sclerotium phenotype, whereas group I strains consisted of both S and L isolates. Based on the omt12 gene region, phylogenetic structure in sclerotium phenotype and aflatoxin production was evident within group I. Some non-aflatoxin producing isolates of group I had an omt12 allele that was identical to that found in isolates of A. oryzae.} }