Akter Sultana, Vehniäinen Markus, Kankaanpää Harri T, Lamminmäki Urpo
Molecular Biotechnology and Diagnostics, Department of Biochemistry, University of Turku, FI-20520 Turku, Finland.
Marine Research Centre, Finnish Environment Institute, Hakuninmaantie 6, FI-00430 Helsinki, Finland.
Microorganisms. 2017 Sep 12;5(3):58. doi: 10.3390/microorganisms5030058.
Nodularin (NOD) is a cyclic penta-peptide hepatotoxin mainly produced by , reported from the brackish water bodies of various parts of the world. It can accumulate in the food chain and, for safety reasons, levels of NOD not only in water bodies but also in food matrices are of interest. Here, we report on a non-competitive immunoassay for the specific detection of NOD. A phage display technique was utilized to interrogate a synthetic antibody phage library for binders recognizing NOD bound to an anti-ADDA (3-Amino-9-methoxy-2,6,8-trimethyl-10-phenyldeca-4(E),6(E)-dienoic acid) monoclonal antibody (Mab). One of the obtained immunocomplex binders, designated SA32C11, showed very high specificity towards nodularin-R (NOD-R) over to the tested 10 different microcystins (microcystin-LR, -dmLR, -RR, -dmRR, -YR, -LY, -LF, -LW, -LA, -WR). It was expressed in as a single chain antibody fragment (scFv) fusion protein and used to establish a time-resolved fluorometry-based assay in combination with the anti-ADDA Mab. The detection limit (blank + 3SD) of the immunoassay, with a total assay time of 1 h 10 min, is 0.03 µg/L of NOD-R. This represents the most sensitive immunoassay method for the specific detection of NOD reported so far. The assay was tested for its performance to detect NOD using spiked (0.1 to 3 µg/L of NOD-R) water samples including brackish sea and coastal water and the recovery ranged from 79 to 127%. Furthermore, a panel of environmental samples, including water from different sources, fish and other marine tissue specimens, were analyzed for NOD using the assay. The assay has potential as a rapid screening tool for the analysis of a large number of water samples for the presence of NOD. It can also find applications in the analysis of the bioaccumulation of NOD in marine organisms and in the food chain.
节球藻毒素(NOD)是一种环状五肽肝毒素,主要由[具体产生者未给出]产生,在世界各地的咸水体中均有报道。它能在食物链中积累,出于安全考虑,不仅水体中,食品基质中的NOD含量也备受关注。在此,我们报道一种用于特异性检测NOD的非竞争性免疫分析方法。利用噬菌体展示技术从合成抗体噬菌体文库中筛选能识别与抗ADDA(3 - 氨基 - 9 - 甲氧基 - 2,6,8 - 三甲基 - 10 - 苯基 - 4(E),6(E) - 二烯酸)单克隆抗体(Mab)结合的NOD的结合物。获得的免疫复合物结合物之一,命名为SA32C11,对节球藻毒素 - R(NOD - R)表现出极高的特异性,相较于测试的10种不同微囊藻毒素(微囊藻毒素 - LR、 - dmLR、 - RR、 - dmRR、 - YR、 - LY、 - LF、 - LW、 - LA、 - WR)。它在[具体表达宿主未给出]中表达为单链抗体片段(scFv)融合蛋白,并与抗ADDA Mab结合用于建立基于时间分辨荧光法的分析方法。该免疫分析方法的检测限(空白 + 3SD)为0.03 μg/L的NOD - R,总分析时间为1小时10分钟。这是迄今为止报道的用于特异性检测NOD的最灵敏的免疫分析方法。使用添加了(0.1至3 μg/L的NOD - R)的水样(包括咸水和沿海水样)测试该分析方法检测NOD的性能,回收率在79%至127%之间。此外,使用该分析方法对包括不同来源的水、鱼类和其他海洋组织标本在内的一组环境样品进行了NOD分析。该分析方法有潜力作为一种快速筛选工具,用于分析大量水样中是否存在NOD。它还可应用于分析NOD在海洋生物和食物链中的生物积累情况。