State Key Laboratory of Agrobiotechnology, Department of Plant Pathology, College of Plant Protection, China Agricultural University, Beijing 100193, China.
College of Agronomy and Biotechnology, China Agricultural University, Beijing 100193, China.
Toxins (Basel). 2022 Sep 23;14(10):659. doi: 10.3390/toxins14100659.
Ustilaginoidins are a class of bis-naphtho-γ-pyrone mycotoxins produced by the pathogen of rice false smut, which has recently become one of the most devastating diseases in rice-growing regions worldwide. In this research, the nanobody phage display library was established after an alpaca was immunized with the hemiustilaginoidin F-hapten coupled with bovine serum albumin (BSA). Heterologous antigen selection and combing trypsin with competition alternant elution methods were performed for nanobody screening. Two nanobodies, namely, Nb-B15 and Nb-C21, were selected for the establishment of indirect competitive enzyme-linked immunosorbent assays (ic-ELISAs). For Nb-B15 and Nb-C21, their IC values were 11.86 μg/mL and 11.22 μg/mL, and the detection ranges were at 3.41-19.98 μg/mL and 1.17-32.13 μg/mL, respectively. Two nanobodies had a broad spectrum to quantify the contents of total ustilaginoidins in rice samples according to cross-reactivity. The recognition mechanisms of Nb-B15 and Nb-C21 against ustilaginoidin A were elucidated by molecular modeling and docking. The key amino acid sites for the binding of Nb-B15 or Nb-C21 to ustilaginoidin A were mainly located in the FR1 and CDR1 regions. As Nb-B15 was superior to Nb-C21 in the aspects of protein expression, ELISA titer, and tolerance to organic solvents, it was selected for application in the detection of actual contaminated rice samples. The total ustilaginoidin contents of rice samples were analyzed by Nb-B15-based ic-ELISA and HPLC-DAD, between which the results were found to be consistent. The developed immunoassay based on the nanobody from the alpaca can be employed as a rapid and effective method for detection of total utilaginoidins in contaminated rice samples.
类脂素是一种由稻曲病菌产生的双萘并-γ-吡喃酮霉菌毒素,该病菌已成为全球水稻种植区最具破坏性的疾病之一。在这项研究中,用半类脂素 F 半抗原与牛血清白蛋白(BSA)偶联物免疫羊驼后,建立了纳米抗体噬菌体展示文库。采用异源抗原选择和胰蛋白酶结合竞争交替洗脱方法进行纳米抗体筛选。筛选出了两个纳米抗体,即 Nb-B15 和 Nb-C21,并建立了间接竞争酶联免疫吸附测定法(ic-ELISA)。对于 Nb-B15 和 Nb-C21,它们的 IC 值分别为 11.86μg/mL 和 11.22μg/mL,检测范围分别为 3.41-19.98μg/mL 和 1.17-32.13μg/mL。这两个纳米抗体具有广谱性,可以根据交叉反应定量测定稻米样品中总类脂素的含量。通过分子建模和对接,阐明了 Nb-B15 和 Nb-C21 识别类脂素 A 的识别机制。Nb-B15 或 Nb-C21 与类脂素 A 结合的关键氨基酸位点主要位于 FR1 和 CDR1 区域。由于 Nb-B15 在蛋白表达、ELISA 效价和有机溶剂耐受性方面优于 Nb-C21,因此选择它用于实际污染稻米样品的检测。基于 Nb-B15 的 ic-ELISA 和 HPLC-DAD 分析了稻米样品中的总类脂素含量,结果一致。基于羊驼纳米抗体开发的免疫分析可以作为一种快速有效的方法,用于检测污染稻米样品中的总类脂素。