Laboratory of Food Safety and Food Integrity, Institute of Tropical Agriculture and Food Security, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia.
Department of Food Science, Faculty of Food Science and Technology, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia.
J Appl Microbiol. 2024 Jun 3;135(6). doi: 10.1093/jambio/lxae145.
The present work aimed to distinguish the indigenous Aspergillus flavus isolates obtained from the first (pioneer) grain corn farms in Terengganu, Malaysia, into aflatoxigenic and non-aflatoxigenic by molecular and aflatoxigenicity analyses, and determine the antagonistic capability of the non-aflatoxigenic isolates against aflatoxigenic counterparts and their aflatoxin production in vitro.
Seven A. flavus isolates previously obtained from the farms were characterized molecularly and chemically. All isolates were examined for the presence of seven aflatoxin biosynthesis genes, and their aflatoxigenicity was confirmed using high performance liquid chromatography with fluorescence detector. Phylogenetic relationships of all isolates were tested using ITS and β-tubulin genes. Of the seven isolates, two were non-aflatoxigenic, while the remaining were aflatoxigenic based on the presence of all aflatoxin biosynthesis genes tested and the productions of aflatoxins B1 and B2. All isolates were also confirmed as A. flavus following phylogenetic analysis. The indigenous non-aflatoxigenic isolates were further examined for their antagonistic potential against aflatoxigenic isolates on 3% grain corn agar. Both non-aflatoxigenic isolates significantly reduced AFB1 production of the aflatoxigenic isolates.
The indigenous non-aflatoxigenic A. flavus strains identified in the present work were effective in controlling the aflatoxin production by the aflatoxigenic A. flavus isolates in vitro and can be utilized for in situ testing.
本研究旨在通过分子和产毒分析,将从马来西亚登嘉楼州首批(先锋)谷物玉米农场分离到的土曲霉本土株系区分产毒和非产毒株系,并确定非产毒株系对产毒株系的拮抗能力及其在体外的产毒能力。
先前从这些农场获得的 7 株 A. flavus 分离株进行了分子和化学特征分析。所有分离株均检测了 7 个黄曲霉生物合成基因的存在情况,并使用高效液相色谱法结合荧光检测器对其产毒情况进行了确认。所有分离株的系统发育关系均采用 ITS 和 β-微管蛋白基因进行了测试。在这 7 株分离株中,有 2 株是非产毒的,而其余的则是产毒的,这是基于所有检测到的黄曲霉生物合成基因的存在以及黄曲霉毒素 B1 和 B2 的产生情况。所有分离株的系统发育分析也证实为 A. flavus。随后对本土非产毒株系在 3%谷物玉米琼脂上对产毒株系的拮抗潜力进行了进一步检测。这两个非产毒株系都显著降低了产毒株系 AFB1 的产生。
本研究中鉴定的本土非产毒 A. flavus 菌株在体外有效控制了产毒 A. flavus 分离株的黄曲霉毒素产生,可用于现场测试。