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Genetic Responses and Aflatoxin Inhibition during Co-Culture of Aflatoxigenic and Non-Aflatoxigenic Aspergillus flavus

Aflatoxin is a carcinogenic mycotoxin produced by Aspergillus flavus. Non-aflatoxigenic (Non-tox) A. flavus isolates are deployed in corn fields as biocontrol because they substantially reduce aflatoxin contamination via direct replacement and additionally via direct contact or touch with toxigenic...

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Autores principales: Sweany, Rebecca R., Mack, Brian M., Moore, Geromy G., Gilbert, Matthew K., Cary, Jeffrey W., Lebar, Matthew D., Rajasekaran, Kanniah, Damann Jr., Kenneth E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8618995/
https://www.ncbi.nlm.nih.gov/pubmed/34822579
http://dx.doi.org/10.3390/toxins13110794
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author Sweany, Rebecca R.
Mack, Brian M.
Moore, Geromy G.
Gilbert, Matthew K.
Cary, Jeffrey W.
Lebar, Matthew D.
Rajasekaran, Kanniah
Damann Jr., Kenneth E.
author_facet Sweany, Rebecca R.
Mack, Brian M.
Moore, Geromy G.
Gilbert, Matthew K.
Cary, Jeffrey W.
Lebar, Matthew D.
Rajasekaran, Kanniah
Damann Jr., Kenneth E.
author_sort Sweany, Rebecca R.
collection PubMed
description Aflatoxin is a carcinogenic mycotoxin produced by Aspergillus flavus. Non-aflatoxigenic (Non-tox) A. flavus isolates are deployed in corn fields as biocontrol because they substantially reduce aflatoxin contamination via direct replacement and additionally via direct contact or touch with toxigenic (Tox) isolates and secretion of inhibitory/degradative chemicals. To understand touch inhibition, HPLC analysis and RNA sequencing examined aflatoxin production and gene expression of Non-tox isolate 17 and Tox isolate 53 mono-cultures and during their interaction in co-culture. Aflatoxin production was reduced by 99.7% in 72 h co-cultures. Fewer than expected unique reads were assigned to Tox 53 during co-culture, indicating its growth and/or gene expression was inhibited in response to Non-tox 17. Predicted secreted proteins and genes involved in oxidation/reduction were enriched in Non-tox 17 and co-cultures compared to Tox 53. Five secondary metabolite (SM) gene clusters and kojic acid synthesis genes were upregulated in Non-tox 17 compared to Tox 53 and a few were further upregulated in co-cultures in response to touch. These results suggest Non-tox strains can inhibit growth and aflatoxin gene cluster expression in Tox strains through touch. Additionally, upregulation of other SM genes and redox genes during the biocontrol interaction demonstrates a potential role of inhibitory SMs and antioxidants as additional biocontrol mechanisms and deserves further exploration to improve biocontrol formulations.
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spelling pubmed-86189952021-11-27 Genetic Responses and Aflatoxin Inhibition during Co-Culture of Aflatoxigenic and Non-Aflatoxigenic Aspergillus flavus Sweany, Rebecca R. Mack, Brian M. Moore, Geromy G. Gilbert, Matthew K. Cary, Jeffrey W. Lebar, Matthew D. Rajasekaran, Kanniah Damann Jr., Kenneth E. Toxins (Basel) Article Aflatoxin is a carcinogenic mycotoxin produced by Aspergillus flavus. Non-aflatoxigenic (Non-tox) A. flavus isolates are deployed in corn fields as biocontrol because they substantially reduce aflatoxin contamination via direct replacement and additionally via direct contact or touch with toxigenic (Tox) isolates and secretion of inhibitory/degradative chemicals. To understand touch inhibition, HPLC analysis and RNA sequencing examined aflatoxin production and gene expression of Non-tox isolate 17 and Tox isolate 53 mono-cultures and during their interaction in co-culture. Aflatoxin production was reduced by 99.7% in 72 h co-cultures. Fewer than expected unique reads were assigned to Tox 53 during co-culture, indicating its growth and/or gene expression was inhibited in response to Non-tox 17. Predicted secreted proteins and genes involved in oxidation/reduction were enriched in Non-tox 17 and co-cultures compared to Tox 53. Five secondary metabolite (SM) gene clusters and kojic acid synthesis genes were upregulated in Non-tox 17 compared to Tox 53 and a few were further upregulated in co-cultures in response to touch. These results suggest Non-tox strains can inhibit growth and aflatoxin gene cluster expression in Tox strains through touch. Additionally, upregulation of other SM genes and redox genes during the biocontrol interaction demonstrates a potential role of inhibitory SMs and antioxidants as additional biocontrol mechanisms and deserves further exploration to improve biocontrol formulations. MDPI 2021-11-11 /pmc/articles/PMC8618995/ /pubmed/34822579 http://dx.doi.org/10.3390/toxins13110794 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sweany, Rebecca R.
Mack, Brian M.
Moore, Geromy G.
Gilbert, Matthew K.
Cary, Jeffrey W.
Lebar, Matthew D.
Rajasekaran, Kanniah
Damann Jr., Kenneth E.
Genetic Responses and Aflatoxin Inhibition during Co-Culture of Aflatoxigenic and Non-Aflatoxigenic Aspergillus flavus
title Genetic Responses and Aflatoxin Inhibition during Co-Culture of Aflatoxigenic and Non-Aflatoxigenic Aspergillus flavus
title_full Genetic Responses and Aflatoxin Inhibition during Co-Culture of Aflatoxigenic and Non-Aflatoxigenic Aspergillus flavus
title_fullStr Genetic Responses and Aflatoxin Inhibition during Co-Culture of Aflatoxigenic and Non-Aflatoxigenic Aspergillus flavus
title_full_unstemmed Genetic Responses and Aflatoxin Inhibition during Co-Culture of Aflatoxigenic and Non-Aflatoxigenic Aspergillus flavus
title_short Genetic Responses and Aflatoxin Inhibition during Co-Culture of Aflatoxigenic and Non-Aflatoxigenic Aspergillus flavus
title_sort genetic responses and aflatoxin inhibition during co-culture of aflatoxigenic and non-aflatoxigenic aspergillus flavus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8618995/
https://www.ncbi.nlm.nih.gov/pubmed/34822579
http://dx.doi.org/10.3390/toxins13110794
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