Small Molecular Contaminant and Microorganism Can Be Simultaneously Detected Based on Nanobody-Phage: Using Carcinogen Aflatoxin and Its Main Fungal Aspergillus Section Flavi spp. in Stored Maize for Demonstration

被引:9
作者
Ren, Xianfeng [1 ,2 ]
Yue, Xiaofeng [1 ,2 ,3 ]
Mwakinyali, Silivano Edson [1 ,2 ,3 ]
Zhang, Wen [1 ,2 ,3 ]
Zhang, Qi [1 ,2 ,3 ]
Li, Peiwu [1 ,2 ,3 ,4 ,5 ]
机构
[1] Chinese Acad Agr Sci, Oil Crops Res Inst, Wuhan, Peoples R China
[2] Minist Agr & Rural Affairs, Key Lab Detect Mycotoxins, Wuhan, Peoples R China
[3] Minist Agr & Rural Affairs, Lab Risk Assessment Oilseeds Prod, Wuhan, Peoples R China
[4] Minist Agr & Rural Affairs, Key Lab Biol & Genet Improvement Oil Crops, Wuhan, Peoples R China
[5] Minist Agr & Rural Affairs, Qual Inspect & Test Ctr Oilseeds Prod, Wuhan, Peoples R China
来源
FRONTIERS IN MICROBIOLOGY | 2020年 / 10卷
基金
中国国家自然科学基金;
关键词
real-time PCR; aflatoxin; Aspergillus; nanobody-phage; Nor-1; gene; REAL-TIME PCR; POLYMERASE-CHAIN-REACTION; SINGLE-DOMAIN ANTIBODY; NOR-1; GENE; IMMUNO-PCR; QUANTIFICATION; RESIDUES; BIOSYNTHESIS; ZEARALENONE; OCHRATOXIN;
D O I
10.3389/fmicb.2019.03023
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Simultaneous detection technology has become a hot topic in analytical chemistry; however, very few reports on how to simultaneously detect small molecular contaminants and microorganisms have been in place. Aflatoxins are a group of highly toxic and carcinogenic compounds, which are produced mainly by Aspergillus flavus and Aspergillus parasiticus from section Flavi responsible for aflatoxin accumulation in stored cereals. Both aflatoxins and Aspergillus section Flavi were used to demonstrate the duplex real-time RCR method of simultaneously detecting small molecular contaminants and microorganisms. The detection of aflatoxins and Aspergillus section Flavi was carried out depending on the anti-idiotypic nanobody-phage V2-5 and aflatoxin-synthesis related gene nor-1 (=aflD), respectively. The quantitative standard curves for simultaneous detection of aflatoxins and Aspergillus section Flavi were constructed, with detection limits of 0.02 ng/ml and 8 x 10(2) spores/g, respectively. Naturally contaminated maize samples (n = 25) were analyzed for a further validation. The results were in good agreement between the new developed method and the referential methods (high-performance liquid chromatography and the conventional plating counts).
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页数:10
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