Events1st International Electronic Conference on Toxins
Published
This submission belongs to the session S7. Poster of the event 1st International Electronic Conference on Toxins
Published date
13 Jan, 2021
Citation
Rebecca Ruth Sweany, Brian M Mack, Geromy G Moore, Matthew K Gilbert, Jeffrey W Cary, Kanniah Rajasekaran, Kenneth E Damann Jr., Genetic responses and aflatoxin inhibition during interaction between aflatoxigenic and non-aflatoxigenic Aspergillus flavus, in Proceedings of 1st International Electronic Conference on Toxins, 16 January–31 January 2021, MDPI: Basel, Switzerland, doi: 10.3390/IECT2021-09117
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Genetic responses and aflatoxin inhibition during interaction between aflatoxigenic and non-aflatoxigenic Aspergillus flavus

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Jeffrey W Cary 1
Kenneth E Damann Jr. 2
1. U.S. Department of Agriculture/ Southern Regional Research Center
2. Louisiana State University
Abstract

Aflatoxin is a carcinogenic mycotoxin produced by Aspergillus flavus in corn. Non-aflatoxigenic A. flavus isolates are applied to corn fields as a biocontrol to reduce aflatoxin contamination. Direct contact or touch between aflatoxigenic and non-aflatoxigenic isolates dramatically reduces aflatoxin production. To understand the mechanism of touch inhibition, a high-throughput RNA-seq study was conducted to examine gene expression during their interaction. Non-aflatoxigenic strain KD17 and aflatoxigenic strain KD53 were grown separately and in co-culture for 30 and 72 h. Toxin production was high in the aflatoxigenic monoculture and negligible in co-cultures. When grown separately, the toxigenic strain represented 7% and 33% of the combined biomass at 30 and 72 h, respectively. However, only 3% of the sequence reads uniquely aligned to the aflatoxigenic strain during co-culture, indicating growth and/or gene expression of the aflatoxigenic strain was inhibited in response to the non-aflatoxigenic strain. Few reads aligned to the aflatoxin gene cluster during co-culture. Eighteen genes expressed during mono-culture of the non-aflatoxigenic strain were further up-regulated during co-culture, indicating a response to contact. Of those genes, seven belong to a putative secondary metabolite cluster, suggesting a potentially inhibitory compound is produced. Taken together, these results suggest that non-aflatoxigenic strains inhibit growth and aflatoxin biosynthetic gene cluster expression in aflatoxin-producing strains. In addition, other secondary metabolite genes are upregulated during biocontrol interaction. This study demonstrates a potential role of inhibitory secondary metabolites in the biocontrol mechanism and deserves further exploration to improve biocontrol formulations.

Keywords
Biocontrol
aflatoxin
toxin inhibition
RNAseq
corn
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