Effects of Zinc Chelators on Aflatoxin Production in Aspergillus parasiticus

Zinc concentrations strongly influence aflatoxin accumulation in laboratory media and in food and feed crops. The presence of zinc stimulates aflatoxin production, and the absence of zinc impedes toxin production. Initial studies that suggested a link between zinc and aflatoxin biosynthesis were pre...

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Main Authors: Josephine Wee, Devin M. Day, John E. Linz
Format: Article
Language:English
Published: MDPI AG 2016-06-01
Series:Toxins
Subjects:
Online Access:http://www.mdpi.com/2072-6651/8/6/171
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spelling doaj-d25981b34a4e4182bcc7a4ec2c97980c2020-11-25T01:04:29ZengMDPI AGToxins2072-66512016-06-018617110.3390/toxins8060171toxins8060171Effects of Zinc Chelators on Aflatoxin Production in Aspergillus parasiticusJosephine Wee0Devin M. Day1John E. Linz2Department of Food Science and Human Nutrition, Michigan State University, East Lansing, MI 48824, USADepartment of Food Science and Human Nutrition, Michigan State University, East Lansing, MI 48824, USADepartment of Food Science and Human Nutrition, Michigan State University, East Lansing, MI 48824, USAZinc concentrations strongly influence aflatoxin accumulation in laboratory media and in food and feed crops. The presence of zinc stimulates aflatoxin production, and the absence of zinc impedes toxin production. Initial studies that suggested a link between zinc and aflatoxin biosynthesis were presented in the 1970s. In the present study, we utilized two zinc chelators, N,N,N′,N′-tetrakis (2-pyridylmethyl) ethane-1,2-diamine (TPEN) and 2,3-dimercapto-1-propanesulfonic acid (DMPS) to explore the effect of zinc limitation on aflatoxin synthesis in Aspergillus parasiticus. TPEN but not DMPS decreased aflatoxin biosynthesis up to six-fold depending on whether A. parasiticus was grown on rich or minimal medium. Although we observed significant inhibition of aflatoxin production by TPEN, no detectable changes were observed in expression levels of the aflatoxin pathway gene ver-1 and the zinc binuclear cluster transcription factor, AflR. Treatment of growing A. parasiticus solid culture with a fluorescent zinc probe demonstrated an increase in intracellular zinc levels assessed by increases in fluorescent intensity of cultures treated with TPEN compared to controls. These data suggest that TPEN binds to cytoplasmic zinc therefore limiting fungal access to zinc. To investigate the efficacy of TPEN on food and feed crops, we found that TPEN effectively decreases aflatoxin accumulation on peanut medium but not in a sunflower seeds-derived medium. From an application perspective, these data provide the basis for biological differences that exist in the efficacy of different zinc chelators in various food and feed crops frequently contaminated by aflatoxin.http://www.mdpi.com/2072-6651/8/6/171Aspergillus parasiticusaflatoxin biosynthesiszinczinc chelators
collection DOAJ
language English
format Article
sources DOAJ
author Josephine Wee
Devin M. Day
John E. Linz
spellingShingle Josephine Wee
Devin M. Day
John E. Linz
Effects of Zinc Chelators on Aflatoxin Production in Aspergillus parasiticus
Toxins
Aspergillus parasiticus
aflatoxin biosynthesis
zinc
zinc chelators
author_facet Josephine Wee
Devin M. Day
John E. Linz
author_sort Josephine Wee
title Effects of Zinc Chelators on Aflatoxin Production in Aspergillus parasiticus
title_short Effects of Zinc Chelators on Aflatoxin Production in Aspergillus parasiticus
title_full Effects of Zinc Chelators on Aflatoxin Production in Aspergillus parasiticus
title_fullStr Effects of Zinc Chelators on Aflatoxin Production in Aspergillus parasiticus
title_full_unstemmed Effects of Zinc Chelators on Aflatoxin Production in Aspergillus parasiticus
title_sort effects of zinc chelators on aflatoxin production in aspergillus parasiticus
publisher MDPI AG
series Toxins
issn 2072-6651
publishDate 2016-06-01
description Zinc concentrations strongly influence aflatoxin accumulation in laboratory media and in food and feed crops. The presence of zinc stimulates aflatoxin production, and the absence of zinc impedes toxin production. Initial studies that suggested a link between zinc and aflatoxin biosynthesis were presented in the 1970s. In the present study, we utilized two zinc chelators, N,N,N′,N′-tetrakis (2-pyridylmethyl) ethane-1,2-diamine (TPEN) and 2,3-dimercapto-1-propanesulfonic acid (DMPS) to explore the effect of zinc limitation on aflatoxin synthesis in Aspergillus parasiticus. TPEN but not DMPS decreased aflatoxin biosynthesis up to six-fold depending on whether A. parasiticus was grown on rich or minimal medium. Although we observed significant inhibition of aflatoxin production by TPEN, no detectable changes were observed in expression levels of the aflatoxin pathway gene ver-1 and the zinc binuclear cluster transcription factor, AflR. Treatment of growing A. parasiticus solid culture with a fluorescent zinc probe demonstrated an increase in intracellular zinc levels assessed by increases in fluorescent intensity of cultures treated with TPEN compared to controls. These data suggest that TPEN binds to cytoplasmic zinc therefore limiting fungal access to zinc. To investigate the efficacy of TPEN on food and feed crops, we found that TPEN effectively decreases aflatoxin accumulation on peanut medium but not in a sunflower seeds-derived medium. From an application perspective, these data provide the basis for biological differences that exist in the efficacy of different zinc chelators in various food and feed crops frequently contaminated by aflatoxin.
topic Aspergillus parasiticus
aflatoxin biosynthesis
zinc
zinc chelators
url http://www.mdpi.com/2072-6651/8/6/171
work_keys_str_mv AT josephinewee effectsofzincchelatorsonaflatoxinproductioninaspergillusparasiticus
AT devinmday effectsofzincchelatorsonaflatoxinproductioninaspergillusparasiticus
AT johnelinz effectsofzincchelatorsonaflatoxinproductioninaspergillusparasiticus
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