产伏马菌素和赭曲霉毒素菌株与尼日利亚西南部市场上出售的洋葱(Allium cepa L.)球茎有关。

IF 2.1 Q3 MYCOLOGY
Frontiers in fungal biology Pub Date : 2025-03-24 eCollection Date: 2025-01-01 DOI:10.3389/ffunb.2025.1563824
Catherine Oluwakemi Esuola, Alejandro Ortega-Beltran
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引用次数: 0

摘要

洋葱是一种可食用的营养丰富的蔬菜和香料。在尼日利亚,由于洋葱鳞茎受到黑曲霉,特别是黑曲霉菌株的感染,洋葱幼苗的大规模繁殖受到限制。产生真菌毒素的黑曲霉菌株对公众健康有害。因此,本研究对当地洋葱进行了福马菌素B2 (FB2) [Multiplex A: fum6 (374 bp), fum8 (272 bp), fum13 (168 bp)和fum19 (479 bp)]和多重plex B: fum1 (452 bp), fum7 (238 bp), fum3 (173 bp)和fum14 (321 bp)]和赭曲霉毒素A [OTA;[776 bp]黑曲霉的生物合成基因。方法:从四个不同的当地市场(Dugbe、Agbowo、Sasa和Omi)收集了100个洋葱鳞茎。每个球茎表面消毒,孵育后检测分离的黑曲霉。在马铃薯葡萄糖琼脂上培养黑曲霉。从分离株中提取基因组DNA。多重PCR证实了FB2 (fum)和OTA (pks15ks)生物合成基因的存在和缺失。结果与讨论:从洋葱鳞茎中分离到200株黑曲霉,其中22株(11%)扩增到至少2个fum基因,3株(1.5%)扩增到pks15ks基因。所有分离株均呈fum1和fum19阳性。fum和pks15ks的定位/分离率最高/最低的分别是Agbowo/Omi(32.0%/2.1%)和Dugbe/Agbowo(6.7%/2.3%)。因此,利用多重PCR检测从当地洋葱鳞茎中分离的黑螺旋藻菌株的FB2和OTA生物合成基因,将有助于洋葱种植者大规模生产具有出口潜力和质量的健康洋葱幼苗。早期检测FB2和OTA生物合成基因对预测洋葱鳞茎中可能产生真菌毒素的A.区段Nigri具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fumonisin and ochratoxin-producing strains of Aspergillus section Nigri are associated with onion (Allium cepa L.) bulbs sold in markets in southwest Nigeria.

Introduction: Onion bulbs are edible, nutritious vegetables and spices. In Nigeria, mass propagation of onion seedlings is limited due to infection of the onion bulbs by Aspergillus section Nigri, especially Aspergillus niger strains. Mycotoxin-producing A. niger strains are detrimental to public health. Hence, this study was undertaken to screen the locally sourced onion bulbs for fumonisin B2 (FB2) [Multiplex A: fum6 (374 bp), fum8 (272 bp), fum13 (168 bp), and fum19 (479 bp) and Multiplex B: fum1 (452 bp), fum7 (238 bp), fum3 (173 bp), and fum14 (321 bp)] and ochratoxin A [OTA; pks15ks (776 bp)] A. niger biosynthetic genes.

Methods: Thus, 100 onion bulbs were collected from four different local markets (Dugbe, Agbowo, Sasa, and Omi). The surface of each bulb was disinfected, and after incubation, isolates of A. niger were detected. A. niger isolates were cultured on potato dextrose agar. Genomic DNA was extracted from isolates of A. niger. Multiplex PCR confirmed the presence and absence of FB2 (fum) and OTA (pks15ks) biosynthetic genes.

Results and discussion: A total of 200 isolates of A. niger were isolated from the onion bulbs, and 22 (11%) isolates amplified at least two fum genes, while three (1.5%) amplified the pks15ks gene. All isolates were positive for fum1 and fum19. The highest/lowest percentage of the location/isolates of fum and pks15ks was Agbowo/Omi with 32.0%/2.1% and Dugbe/Agbowo with 6.7%/2.3%, respectively. Hence, the use of multiplex PCR to detect FB2 and OTA biosynthetic genes in the isolated A. niger strains from the locally sourced onion bulbs will assist onion growers in the mass production of healthy onion seedlings with export potential and quality. Early detection of FB2 and OTA biosynthetic genes is important to predict possible mycotoxin-producing A. section Nigri in onion bulbs.

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