Inhibition of Aspergillus flavus Growth and Aflatoxin Production in Transgenic Maize Expressing the α-amylase Inhibitor from Lablab purpureus L.

被引:9
作者
Rajasekaran, Kanniah [1 ]
Sayler, Ronald J. [2 ]
Majumdar, Rajtilak [1 ]
Sickler, Christine M. [1 ]
Cary, Jeffrey W. [1 ]
机构
[1] USDA ARS, Southern Reg Res Ctr, Food & Feed Safety Res Unit, Washington, DC 20250 USA
[2] Univ Arkansas, Dept Plant Pathol, Fayetteville, AR 72701 USA
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2019年 / 144期
关键词
Environmental Sciences; Issue; 144; alpha-amylase inhibitor; aflatoxin; Aspergillus flavus; corn; kernel screening assay; Lablab purpureus; maize; transgenic; LECTIN; GENE; CONTAMINATION; COLONIZATION; RESISTANCE; BIOSYNTHESIS; TECHNOLOGIES; KERNELS; PROTEIN; LOSSES;
D O I
10.3791/59169
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Aflatoxin contamination in food and feed crops is a major challenge worldwide. Aflatoxins, produced by the fungus Aspergillus flavus (A. flavus) are potent carcinogens that substantially reduce crop value in maize and other oil rich crops like peanut besides posing serious threat to human and animal health. Different approaches, including traditional breeding, transgenic expression of resistance associated proteins, and RNA interference (RNAi)-based host-induced gene silencing of critical A. flavus gene targets, are being evaluated to increase aflatoxin resistance in susceptible crops. Past studies have shown an important role of alpha-amylase in A. flavus pathogenesis and aflatoxin production, suggesting this gene/enzyme is a potential target to reduce both A. flavus growth and aflatoxin production. In this regard, the current study was undertaken to evaluate heterologous expression (under control of the constitutive CaMV 35S promoter) of a Lablab purpureus L. alpha-amylase inhibitor-like protein (AILP) in maize against A. flavus. AILP is a 36-kDa protein, which is a competitive inhibitor of A. flavus alpha-amylase enzyme and belongs to the lectin-arcelin-alpha-amylase inhibitor protein family in common bean. In vitro studies prior to the current work had demonstrated the role of AILP in inhibition of A. flavus alpha-amylase activity and fungal growth. Fungal growth and aflatoxin production in mature kernels were monitored in real time using a GFP-expressing A. flavus strain. This kernel screening assay (KSA) is very simple to set up and provides reliable and reproducible data on infection and the extent of spread that could be quantified for evaluation of germplasm and transgenic lines. The fluorescence from the GFP strain is closely correlated to fungal growth and, by extension, it is well-correlated to aflatoxin values. The goal of the current work was to implement this previous knowledge in a commercially important crop like maize to increase aflatoxin resistance. Our results show a 35%-72% reduction in A. flavus growth in AILP-expressing transgenic maize kernels which, in turn, translated into a 62%-88% reduction in aflatoxin levels.
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页数:12
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