Mode of action of pesticides on aflatoxin biosynthesis and oxidase system activity
1Botany Department, Faculty of Science, Assiut University, Egypt.
Abstract:
The effects of nine pesticides on the biosynthesis of aflatoxin and oxidase activity in wild-type Aspergillus flavus and mutant strains of A. parasiticus avr-1 (w 49) and A. parasiticus ver-1 (wh 1) were investigated. In A. parasiticus, phosphonic acid derivative (lancer) reduced the formation of aflatoxin B2 but B1, G1 and G2 and anthraquinones (versicolorin A, versiconal hemiacetal acetat and averufin) accumulated. Phosphorothioic acid derivatives (pirimiphos-methyl and pyrazophos) reduced the formation of aflatoxin B2 and G2 but B1 and G1 and anthraquinones accumulated. Phosphorodithioic acid derivatives (dimethoate and malathion) blocked aflatoxin B2, reduced B1 and G2 but G1 and anthraquinones accumulated. Phosphoric acid derivative (profenfos) inhibited the formation of all aflatoxins, versicolorin A and versiconal hemiacetal acetate but averufin accumulated. The phenylurea derivatives (linuron and pencycuron) at concentrations of 500 and 1000 ppm inhibited all aflatoxin but anthraquinones accumulated. On the other hand, the dicarboximide derivative (iprodione) inhibited the whole pathway in the mutant strains of A. parasiticus. The oxidase system in wild-type A. flavus was active in the conversion of averufin and versicolorin A into aflatoxin B1. Most organophosphate and phenylurea derivatives may competitively increase or decrease the oxidase enzymes, however, profenfos and iprodione blocked the enzymes between averufin and versicolorin A.
Insights
Nine pesticides were tested for their impact on aflatoxin production in Aspergillus species. Some pesticides inhibited specific aflatoxins while allowing others to accumulate, with iprodione halting the entire pathway in mutant strains.
Area of Science:
- Mycology
- Food Science
- Toxicology
Background:
- Aflatoxins are toxic secondary metabolites produced by Aspergillus species.
- Pesticide use can potentially influence fungal metabolism and toxin production.
- Understanding these interactions is crucial for food safety and agricultural practices.
Purpose of the Study:
- To investigate the effects of nine different pesticides on aflatoxin biosynthesis.
- To examine the impact of these pesticides on oxidase activity in Aspergillus flavus and mutant strains.
- To determine which pesticide classes and specific compounds inhibit or alter aflatoxin production pathways.
Main Methods:
- Tested nine pesticides against wild-type Aspergillus flavus and mutant strains (A. parasiticus avr-1, A. parasiticus ver-1).
- Quantified aflatoxin (B1, B2, G1, G2) and anthraquinone (versicolorin A, versiconal hemiacetal acetate, averufin) biosynthesis.
- Assessed oxidase enzyme activity involved in aflatoxin production.
Main Results:
- Different pesticide classes exhibited varied effects on aflatoxin and anthraquinone accumulation.
- Phosphonic, phosphorothioic, phosphorodithioic, and phosphoric acid derivatives showed differential inhibition of aflatoxins and accumulation of intermediates.
- Phenylurea derivatives (linuron, pencycuron) inhibited all aflatoxins, while iprodione completely blocked the pathway in mutant strains.
- Oxidase activity was linked to averufin and versicolorin A conversion; profenfos and iprodione inhibited enzymes in this pathway.
Conclusions:
- Pesticides have diverse impacts on aflatoxin biosynthesis pathways in Aspergillus.
- Specific pesticide chemistries, like iprodione and profenfos, can significantly disrupt aflatoxin production.
- Further research is needed to understand the mechanisms and implications of these interactions for food safety.
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