Mechanisms of methyl 2-methylbutyrate suppression on Aspergillus flavus growth and aflatoxin B1 biosynthesis.

Aflatoxins Aspergillus flavus Food crops Methyl 2-methylbutyrate Transcriptomics analysis

Journal

International journal of food microbiology
ISSN: 1879-3460
Titre abrégé: Int J Food Microbiol
Pays: Netherlands
ID NLM: 8412849

Informations de publication

Date de publication:
16 Jan 2024
Historique:
received: 02 08 2023
revised: 17 10 2023
accepted: 26 10 2023
medline: 23 11 2023
pubmed: 3 11 2023
entrez: 2 11 2023
Statut: ppublish

Résumé

Aspergillus flavus and subsequently produced carcinogenic aflatoxins frequently contaminate postharvest food crops, resulting in a threat to global food safety. Chemical preservatives are currently the main antifungal agents. However, fungal resistance effect, biological toxicity, and environmental contamination limit their practical applications. The application of natural volatile organic compounds has great potential for controlling fungal and mycotoxin contamination of postharvest food crops. This study therefore investigated the antifungal and anti-aflatoxigenic activities of the volatile compound, methyl 2-methylbutyrate (M2M), against Aspergillus flavus and its potential mechanisms. M2M effectively inhibited A. flavus mycelia growth, with a minimum inhibitory concentration of 2.0 μL/mL. Moreover, M2M also suppressed aflatoxin production, sclerotia production, and the pathogenicity on peanut and corn flour. RNA-Seq results showed that 2899 differentially expressed genes (DEGs), and DEGs involved in ergosterol synthesis, cell wall structure, glycolysis, citric acid cycle, mitogen activated protein kinase signaling pathway, DNA replication, and aflatoxin biosynthesis, were down-regulated in A. flavus. Further studies showed that M2M strongly damaged the cell membrane and cell wall integrity, reduced ATP levels, and induced reactive oxygen species (ROS) accumulation and DNA damage. Notably, a GATA type zinc finger transcription factor, AfSreA (AFLA_132440), which is essential for A. flavus growth and aflatoxin production, was identified. The growth and aflatoxin yield in the ΔAfSreA strain decreased by 94.94 % and 71.82 %, respectively. Additionally, deletion of AfSreA destroyed cell wall integrity and decreased expressions of genes involved in aflatoxin biosynthesis. Taken together, our results identified the antifungal and anti-aflatoxigenic mechanisms of M2M against A. flavus, and confirmed the potential of M2M in protecting peanut and corn from fungal contamination.

Identifiants

pubmed: 37918192
pii: S0168-1605(23)00379-3
doi: 10.1016/j.ijfoodmicro.2023.110462
pii:
doi:

Substances chimiques

Aflatoxin B1 9N2N2Y55MH
2-methylbutanoic acid PX7ZNN5GXK
Antifungal Agents 0
Aflatoxins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

110462

Informations de copyright

Copyright © 2023 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare no competing interests.

Auteurs

Shan Wei (S)

College of Bioengineering, Henan University of Technology, Zhengzhou 450001, PR China.

Yige Zhang (Y)

College of Bioengineering, Henan University of Technology, Zhengzhou 450001, PR China.

Menghan Wu (M)

College of Bioengineering, Henan University of Technology, Zhengzhou 450001, PR China.

Yangyong Lv (Y)

College of Bioengineering, Henan University of Technology, Zhengzhou 450001, PR China.

Shuaibing Zhang (S)

College of Bioengineering, Henan University of Technology, Zhengzhou 450001, PR China.

Huanchen Zhai (H)

College of Bioengineering, Henan University of Technology, Zhengzhou 450001, PR China.

Yuansen Hu (Y)

College of Bioengineering, Henan University of Technology, Zhengzhou 450001, PR China; Food Laboratory of Zhongyuan, Henan University of Technology, Luohe 462300, PR China. Electronic address: huyuansen@haut.edu.cn.

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Classifications MeSH