Levels of mycotoxins produced by
Fusarium species in genetically modified (GM) and near-isogenic maize, were determined using multi-analyte, microbead-based flow immunocytometry with fluorescence detection, for the parallel quantitative determination of fumonisin B1, deoxynivalenol, zearalenone, T-2, ochratoxin A, and aflatoxin B1. Maize varieties included
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Levels of mycotoxins produced by
Fusarium species in genetically modified (GM) and near-isogenic maize, were determined using multi-analyte, microbead-based flow immunocytometry with fluorescence detection, for the parallel quantitative determination of fumonisin B1, deoxynivalenol, zearalenone, T-2, ochratoxin A, and aflatoxin B1. Maize varieties included the genetic events
MON 810 and
DAS-59122-7, and their isogenic counterparts. Cobs were artificially infested by
F. verticillioides and
F. proliferatum conidia, and contained
F. graminearum and
F. sporotrichoides natural infestation. The production of fumonisin B1 and deoxynivalenol was substantially affected in GM maize lines:
F. verticillioides, with the addition of
F. graminearum and
F. sporotrichoides, produced significantly lower levels of fumonisin B1 (~300 mg·kg
−1) in
DAS-59122-7 than in its isogenic line (~580 mg·kg
−1), while
F. proliferatum, in addition to
F. graminearum and
F. sporotrichoides, produced significantly higher levels of deoxynivalenol (~18 mg·kg
−1) in
MON 810 than in its isogenic line (~5 mg·kg
−1).
Fusarium verticillioides, with
F. graminearum and
F. sporotrichoides, produced lower amounts of deoxynivalenol and zearalenone than
F. proliferatum, with
F. graminearum and
F. sporotrichoides. T-2 toxin production remained unchanged when considering the maize variety. The results demonstrate the utility of the Fungi-Plex™ quantitative flow immunocytometry method, applied for the high throughput parallel determination of the target mycotoxins.
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