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香薷挥发油对产毒寄生曲霉生长、黄曲霉毒素合成及相关基因转录的影响

The potential effects of Zataria multiflora Boiss essential oil on growth, aflatoxin production and transcription of aflatoxin biosynthesis pathway genes of toxigenic Aspergillus parasiticus.

机构信息

Mycology Research Centre, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran.

出版信息

Braz J Microbiol. 2013 Oct 30;44(2):643-9. doi: 10.1590/S1517-83822013000200045. eCollection 2013.

DOI:10.1590/S1517-83822013000200045
PMID:24294264
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3833170/
Abstract

This study aims at evaluating the effects of Zataria multiflora (Z. multiflora) essential oil (EO) on growth, aflatoxin production and transcription of aflatoxin biosynthesis pathway genes. Total RNAs of Aspergillus parasiticus (A.parasiticus) ATCC56775 grown in yeast extract sucrose (YES) broth medium treated with Z. multiflora EO were subjected to reverse transcription- polymerase chain reaction (RT-PCR). Specific primers of nor-1, ver-1, omt-A and aflR genes were used. In parallel mycelial dry weight of samples were measured and all the media were assayed by high-pressure liquid chromatography (HPLC) for aflatoxinB1 (AFB1), aflatoxinB2 (AFB2), aflatoxinG1 (AFG1), aflatoxinG2 (AFG2) and aflatoxin total (AFTotal) production. The results showed that mycelial dry weight and aflatoxin production reduce in the presence of Z. multiflora EO (100 ppm) on day 5 of growth. It was found that the expression of nor-1, ver-1, omt-A and aflR genes was correlated with the ability of fungus to produce aflatoxins on day 5 in YES medium. RT-PCR showed that in the presence of Z.multiflora EO (100 ppm) nor-1, ver-1 and omtA genes expression was reduced. It seems that toxin production inhibitory effects of Z. multiflora EO on day 5 may be at the transcription level and this herb may cause reduction in aflatoxin biosynthesis pathway genes activity.

摘要

本研究旨在评估香薷(Zataria multiflora)精油(EO)对生长、黄曲霉毒素产生和黄曲霉毒素生物合成途径基因转录的影响。在酵母提取物蔗糖(YES)培养基中生长的寄生曲霉(A.parasiticus)ATCC56775 的总 RNA 用香薷精油(Z. multiflora EO)处理后,进行逆转录-聚合酶链反应(RT-PCR)。使用 nor-1、ver-1、omt-A 和 aflR 基因的特异性引物。同时,测量样品的菌丝干重,并通过高压液相色谱(HPLC)对所有培养基进行分析,以测定黄曲霉毒素 B1(AFB1)、黄曲霉毒素 B2(AFB2)、黄曲霉毒素 G1(AFG1)、黄曲霉毒素 G2(AFG2)和黄曲霉毒素总量(AFTotal)的产生。结果表明,在第 5 天生长时,香薷精油(100ppm)存在时,菌丝干重和黄曲霉毒素产量减少。发现 nor-1、ver-1、omt-A 和 aflR 基因的表达与真菌在 YES 培养基中第 5 天产生黄曲霉毒素的能力相关。RT-PCR 显示,在香薷精油(100ppm)存在的情况下,nor-1、ver-1 和 omtA 基因的表达减少。似乎香薷精油对第 5 天的毒素产生抑制作用可能是在转录水平上,这种草药可能会降低黄曲霉毒素生物合成途径基因的活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd10/3833170/ca2ed858ca02/bjm-44-643-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd10/3833170/ca2ed858ca02/bjm-44-643-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cd10/3833170/ca2ed858ca02/bjm-44-643-g001.jpg

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