Department of Soil, Plant and Food Sciences, University of Bari Aldo Moro, Via Giovanni Amendola, 165/A, 70126 Bari, Italy.
Food Biotechnology Department, Instituto de Agroquímica y Tecnología de Alimentos (IATA-CSIC), Calle Catedrático Agustín Escardino 7, 46980 Paterna, Valencia, Spain.
Toxins (Basel). 2021 Feb 2;13(2):111. doi: 10.3390/toxins13020111.
is the principal fungal species responsible for ochratoxin A (OTA) contamination of grapes and derived products in the main viticultural regions worldwide. In recent years, co-expressed genes representing a putative-OTA gene cluster were identified, and the deletion of a few of them allowed the partial elucidation of the biosynthetic pathway in the fungus. In the putative OTA-gene cluster is additionally present a bZIP transcription factor (), and with this work, Δ strains were generated to study its functional role. According to phylogenetic analysis, the gene is conserved in the OTA-producing fungi. A transcription factor binding motif (TFBM) homolog, associated with bZIP transcription factors was present in the OTA-gene cluster no-coding regions. deletion results in the loss of OTA and the intermediates OTB and OTβ. Additionally, in Δ strains, a down-regulation of , , , and genes was observed compared to wild type (WT). These results provide evidence of the direct involvement of the gene in the OTA biosynthetic pathway by regulating the involved genes. The loss of OTA biosynthesis ability does not affect fungal development as demonstrated by the comparison of Δ strains and WT strains in terms of vegetative growth and asexual sporulation on three different media. Finally, no statistically significant differences in virulence were observed among Δ strains and WT strains on artificially inoculated grape berries, demonstrating that OTA is not required by for the pathogenicity process.
是世界主要葡萄种植区葡萄及其衍生产品中赭曲霉毒素 A (OTA) 污染的主要真菌物种。近年来,鉴定出了代表假定 OTA 基因簇的共表达基因,并且删除其中的一些基因允许部分阐明真菌中的生物合成途径。在假定的 OTA 基因簇中还存在一个 bZIP 转录因子(),通过这项工作,生成了 Δ 菌株来研究其功能作用。根据系统发育分析,该基因在产生 OTA 的真菌中是保守的。在 OTA 基因簇的非编码区域中存在与 bZIP 转录因子相关的 bZIP 转录因子结合基序 (TFBM) 同源物。缺失导致 OTA 和中间产物 OTB 和 OTβ 的丢失。此外,与野生型 (WT) 相比,在 Δ 菌株中观察到 、 、 和 基因的下调。这些结果提供了证据表明 基因通过调节相关基因直接参与 OTA 生物合成途径。OTA 生物合成能力的丧失并不影响真菌的发育,这可以通过比较 Δ 菌株和 WT 菌株在三种不同培养基上的营养生长和无性孢子形成来证明。最后,在人工接种的葡萄浆果上,Δ 菌株和 WT 菌株之间的毒力没有观察到统计学上的显著差异,表明 OTA 不是 致病过程所必需的。