Effects of Hydrogen Peroxide on Different Toxigenic and Atoxigenic Isolates of Aspergillus flavus

Drought stress in the field has been shown to exacerbate aflatoxin contamination of maize and peanut. Drought and heat stress also produce reactive oxygen species (ROS) in plant tissues. Given the potential correlation between ROS and exacerbated aflatoxin production under drought and heat stress, t...

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Main Authors: Jake C. Fountain, Brian T. Scully, Zhi-Yuan Chen, Scott E. Gold, Anthony E. Glenn, Hamed K. Abbas, R. Dewey Lee, Robert C. Kemerait, Baozhu Guo
Format: Article
Language:English
Published: MDPI AG 2015-08-01
Series:Toxins
Subjects:
Online Access:http://www.mdpi.com/2072-6651/7/8/2985
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author Jake C. Fountain
Brian T. Scully
Zhi-Yuan Chen
Scott E. Gold
Anthony E. Glenn
Hamed K. Abbas
R. Dewey Lee
Robert C. Kemerait
Baozhu Guo
author_facet Jake C. Fountain
Brian T. Scully
Zhi-Yuan Chen
Scott E. Gold
Anthony E. Glenn
Hamed K. Abbas
R. Dewey Lee
Robert C. Kemerait
Baozhu Guo
author_sort Jake C. Fountain
collection DOAJ
description Drought stress in the field has been shown to exacerbate aflatoxin contamination of maize and peanut. Drought and heat stress also produce reactive oxygen species (ROS) in plant tissues. Given the potential correlation between ROS and exacerbated aflatoxin production under drought and heat stress, the objectives of this study were to examine the effects of hydrogen peroxide (H2O2)-induced oxidative stress on the growth of different toxigenic (+) and atoxigenic (−) isolates of Aspergillus flavus and to test whether aflatoxin production affects the H2O2 concentrations that the isolates could survive. Ten isolates were tested: NRRL3357 (+), A9 (+), AF13 (+), Tox4 (+), A1 (−), K49 (−), K54A (−), AF36 (−), and Aflaguard (−); and one A. parasiticus isolate, NRRL2999 (+). These isolates were cultured under a H2O2 gradient ranging from 0 to 50 mM in two different media, aflatoxin-conducive yeast extract-sucrose (YES) and non-conducive yeast extract-peptone (YEP). Fungal growth was inhibited at a high H2O2 concentration, but specific isolates grew well at different H2O2 concentrations. Generally the toxigenic isolates tolerated higher concentrations than did atoxigenic isolates. Increasing H2O2 concentrations in the media resulted in elevated aflatoxin production in toxigenic isolates. In YEP media, the higher concentration of peptone (15%) partially inactivated the H2O2 in the media. In the 1% peptone media, YEP did not affect the H2O2 concentrations that the isolates could survive in comparison with YES media, without aflatoxin production. It is interesting to note that the commercial biocontrol isolates, AF36 (−), and Aflaguard (−), survived at higher levels of stress than other atoxigenic isolates, suggesting that this testing method could potentially be of use in the selection of biocontrol isolates. Further studies will be needed to investigate the mechanisms behind the variability among isolates with regard to their degree of oxidative stress tolerance and the role of aflatoxin production.
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spelling doaj.art-46d016f86a0d4b32a164ed5b5304b9c42022-12-22T02:21:21ZengMDPI AGToxins2072-66512015-08-01782985299910.3390/toxins7082985toxins7082985Effects of Hydrogen Peroxide on Different Toxigenic and Atoxigenic Isolates of Aspergillus flavusJake C. Fountain0Brian T. Scully1Zhi-Yuan Chen2Scott E. Gold3Anthony E. Glenn4Hamed K. Abbas5R. Dewey Lee6Robert C. Kemerait7Baozhu Guo8Department of Plant Pathology, University of Georgia, Tifton, GA 31793, USAUSDA-ARS, U.S. Horticultural Research Laboratory, Fort Pierce, FL 34945, USADepartment of Plant Pathology and Crop Physiology, Louisiana State University, Baton Rouge, LA 70803, USAUSDA-ARS, Toxicology and Mycotoxin Research Unit, Athens, GA 30605, USAUSDA-ARS, Toxicology and Mycotoxin Research Unit, Athens, GA 30605, USAUSDA-ARS, Biological Control of Pests Research Unit, Stoneville, MS 38776, USADepartment of Crop and Soil Sciences, University of Georgia, Tifton, GA 31793, USADepartment of Plant Pathology, University of Georgia, Tifton, GA 31793, USAUSDA-ARS, Crop Protection and Management Research Unit, Tifton, GA 31793, USADrought stress in the field has been shown to exacerbate aflatoxin contamination of maize and peanut. Drought and heat stress also produce reactive oxygen species (ROS) in plant tissues. Given the potential correlation between ROS and exacerbated aflatoxin production under drought and heat stress, the objectives of this study were to examine the effects of hydrogen peroxide (H2O2)-induced oxidative stress on the growth of different toxigenic (+) and atoxigenic (−) isolates of Aspergillus flavus and to test whether aflatoxin production affects the H2O2 concentrations that the isolates could survive. Ten isolates were tested: NRRL3357 (+), A9 (+), AF13 (+), Tox4 (+), A1 (−), K49 (−), K54A (−), AF36 (−), and Aflaguard (−); and one A. parasiticus isolate, NRRL2999 (+). These isolates were cultured under a H2O2 gradient ranging from 0 to 50 mM in two different media, aflatoxin-conducive yeast extract-sucrose (YES) and non-conducive yeast extract-peptone (YEP). Fungal growth was inhibited at a high H2O2 concentration, but specific isolates grew well at different H2O2 concentrations. Generally the toxigenic isolates tolerated higher concentrations than did atoxigenic isolates. Increasing H2O2 concentrations in the media resulted in elevated aflatoxin production in toxigenic isolates. In YEP media, the higher concentration of peptone (15%) partially inactivated the H2O2 in the media. In the 1% peptone media, YEP did not affect the H2O2 concentrations that the isolates could survive in comparison with YES media, without aflatoxin production. It is interesting to note that the commercial biocontrol isolates, AF36 (−), and Aflaguard (−), survived at higher levels of stress than other atoxigenic isolates, suggesting that this testing method could potentially be of use in the selection of biocontrol isolates. Further studies will be needed to investigate the mechanisms behind the variability among isolates with regard to their degree of oxidative stress tolerance and the role of aflatoxin production.http://www.mdpi.com/2072-6651/7/8/2985aflatoxindroughtoxidative stressreactive oxygen speciesbiological controlspeptone
spellingShingle Jake C. Fountain
Brian T. Scully
Zhi-Yuan Chen
Scott E. Gold
Anthony E. Glenn
Hamed K. Abbas
R. Dewey Lee
Robert C. Kemerait
Baozhu Guo
Effects of Hydrogen Peroxide on Different Toxigenic and Atoxigenic Isolates of Aspergillus flavus
Toxins
aflatoxin
drought
oxidative stress
reactive oxygen species
biological controls
peptone
title Effects of Hydrogen Peroxide on Different Toxigenic and Atoxigenic Isolates of Aspergillus flavus
title_full Effects of Hydrogen Peroxide on Different Toxigenic and Atoxigenic Isolates of Aspergillus flavus
title_fullStr Effects of Hydrogen Peroxide on Different Toxigenic and Atoxigenic Isolates of Aspergillus flavus
title_full_unstemmed Effects of Hydrogen Peroxide on Different Toxigenic and Atoxigenic Isolates of Aspergillus flavus
title_short Effects of Hydrogen Peroxide on Different Toxigenic and Atoxigenic Isolates of Aspergillus flavus
title_sort effects of hydrogen peroxide on different toxigenic and atoxigenic isolates of aspergillus flavus
topic aflatoxin
drought
oxidative stress
reactive oxygen species
biological controls
peptone
url http://www.mdpi.com/2072-6651/7/8/2985
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