Center for Applied Geosciences, Eberhard Karls Universität Tübingen, Hölderlinstr. 12, 72074 Tübingen, Germany.
BCCM/ULC, University of Liege, In-Bios Centre for Protein Engineering, B6, 4000 Liege, Belgium.
Toxins (Basel). 2018 Apr 3;10(4):147. doi: 10.3390/toxins10040147.
Cyanobacteria synthesize a large variety of secondary metabolites including toxins. Microcystins (MCs) with hepato- and neurotoxic potential are well studied in bloom-forming planktonic species of temperate and tropical regions. Cyanobacterial biofilms thriving in the polar regions have recently emerged as a rich source for cyanobacterial secondary metabolites including previously undescribed congeners of microcystin. However, detection and detailed identification of these compounds is difficult due to unusual sample matrices and structural congeners produced. We here report a time-efficient liquid chromatography-mass spectrometry (LC-MS) precursor ion screening method that facilitates microcystin detection and identification. We applied this method to detect six different MC congeners in 8 out of 26 microbial mat samples of the Svalbard Archipelago in the Arctic. The congeners, of which [Asp³, ADMAdda⁵, Dhb⁷] MC-LR was most abundant, were similar to those reported in other polar habitats. Microcystins were also determined using an Adda-specific enzyme-linked immunosorbent assay (Adda-ELISA). sp. was identified as a putative toxin producer using molecular methods that targeted 16S rRNA genes and genes involved in microcystin production. The genes detected showed highest similarities to other Arctic or Antarctic sequences. The LC-MS precursor ion screening method could be useful for microcystin detection in unusual matrices such as benthic biofilms or lichen.
蓝藻合成多种次生代谢物,包括毒素。微囊藻毒素(MCs)具有潜在的肝毒性和神经毒性,在温带和热带地区的浮游性蓝藻水华种中得到了广泛研究。在极地地区繁盛的蓝藻生物膜最近成为蓝藻次生代谢物的丰富来源,包括以前未描述的微囊藻毒素同系物。然而,由于不常见的样品基质和产生的结构同系物,这些化合物的检测和详细鉴定具有挑战性。我们在这里报告了一种高效液相色谱-质谱(LC-MS)前体离子筛选方法,该方法可促进微囊藻毒素的检测和鉴定。我们将该方法应用于检测北极斯瓦尔巴群岛 26 个微生物垫样本中的 8 个样本中的 6 种不同的 MC 同系物。这些同系物中,[Asp³, ADMAdda⁵, Dhb⁷] MC-LR 最为丰富,与其他极地生境中报道的同系物相似。使用针对 16S rRNA 基因和参与微囊藻毒素生产的基因的 Adda 特异性酶联免疫吸附测定(Adda-ELISA)也确定了微囊藻毒素的存在。sp. 被鉴定为潜在的毒素生产者,使用靶向 16S rRNA 基因和参与微囊藻毒素生产的基因的分子方法。检测到的基因与其他北极或南极序列具有最高相似性。LC-MS 前体离子筛选方法可用于检测底栖生物膜或地衣等不常见基质中的微囊藻毒素。