Transcriptome analysis of Ochratoxin a (OTA) producing Aspergillus westerdijkiae fc-1 under varying osmotic pressure.

IF 4.4 2区 生物学 Q1 MYCOLOGY
Mycology Pub Date : 2024-10-29 eCollection Date: 2025-01-01 DOI:10.1080/21501203.2024.2408259
Yanling Ma, Muyuan Zhuang, Tanvir Ahmad, Mingxuan Li, Guangyou Tan, Yingyao Deng, Yang Liu
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Abstract

Ochratoxin A (OTA) is a toxic secondary metabolite produced by the Aspergillus species which can contaminate various food products. This study analysed the transcriptome of the Aspergillus westerdijkiae fc-1 strain under NaCl concentrations of 0, 20, and 100 g/L using RNA-Seq technology to examine gene transcriptional changes linked to osmotic stress and OTA production. Significant changes were observed in metabolic-pathways associated with carbohydrates, cellular communication, and hydrolase activity under 20 g/L NaCl. The HOG1 gene, associated with osmotic pressure regulation was down-regulated by 78.06%. In contrast, OTA biosynthesis genes otaA, otaB, and otaC were up-regulated by 3.26 fold, 1.99 fold, and 2.06 fold, respectively. Conversely, the otaD gene was down-regulated by 43.50%. At 100 g/L NaCl, pathways related to ion transport, peptide metabolism, ribosomal function, and transmembrane transporter protein activities were significantly up-regulated. The HOG1 gene was up-regulated by 28.32% and OTA biosynthesis genes otaA, otaB, otaC, and otaD showed up-regulation of 27.06%, 36.80%, 19.59%, and 5.72 fold, respectively. The study highlights the role of metabolic pathways in osmotic stress regulation and the correlations between HOG1 expression and OTA biosynthesis genes, providing insights for developing strategies to prevent OTA contamination in food.

不同渗透压下产生赭曲霉毒素a (OTA)的西部曲霉fc-1的转录组分析。
赭曲霉毒素A (Ochratoxin A, OTA)是曲霉产生的有毒次生代谢物,可污染多种食品。本研究利用RNA-Seq技术分析了NaCl浓度为0、20和100 g/L的西曲霉fc-1菌株的转录组,以检测渗透胁迫和OTA产生相关的基因转录变化。在20 g/L NaCl处理下,与碳水化合物、细胞通讯和水解酶活性相关的代谢途径发生了显著变化。与渗透压调节相关的HOG1基因下调78.06%。相比之下,OTA生物合成基因otaA、otaB和otaC分别上调3.26倍、1.99倍和2.06倍。相反,otaD基因下调43.50%。在100 g/L NaCl处理下,与离子转运、肽代谢、核糖体功能和跨膜转运蛋白活性相关的途径显著上调。HOG1基因上调28.32%,OTA生物合成基因otaA、otaB、otaC和otaD分别上调27.06%、36.80%、19.59%和5.72倍。该研究强调了代谢途径在渗透胁迫调节中的作用,以及HOG1表达与OTA生物合成基因之间的相关性,为制定防止食品中OTA污染的策略提供了见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Mycology
Mycology Medicine-Infectious Diseases
CiteScore
9.10
自引率
0.00%
发文量
18
审稿时长
13 weeks
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