Battelle Memorial Institute, 505 King Ave, Columbus, OH 43201, USA; Emergency Response Branch, Division of Laboratory Sciences, National Center for Environmental Health, Centers for Disease Control and Prevention, 4770 Buford Hwy NE, Atlanta, GA 30341, USA.
Biotoxin Metrology, National Research Council Canada, 1411 Oxford Street, Halifax, NS, B3H 3Z1, Canada; Chemistry and Toxinology Research Group, Norwegian Veterinary Institute, Elizabeth Stephansens vei 1, 1433 Ås, Norway.
Harmful Algae. 2024 Nov;139:102739. doi: 10.1016/j.hal.2024.102739. Epub 2024 Oct 22.
Microcystins are an emergent public health problem. These toxins are secondary metabolites of harmful cyanobacterial blooms, with blooms becoming more prevalent with eutrophication of water. Exposure to microcystins can result in sickness, liver damage, and even death. Over 300 microcystins have been identified to date, with differences in toxicity based on the specific amino acid composition. Because of this diversity in microcystins, as well as the likelihood of detecting as yet undiscovered microcystins, it is vital to establish a methodological workflow to identify any microcystin in a complex sample, regardless of the availability of a reference standard. Additionally, ascribing varying levels of confidence to these identifications is critical to effectively communicate discoveries.
A liquid-chromatography-high-resolution mass spectrometry method was utilized to identify microcystins present in cyanobacterial extracts from a strain of Microcystis aeruginosa and an Aphanizomenon sp. First, microcystin congeners with available standards were identified in the cyanobacterial extract. These known-unknown microcystins were considered to have the highest confidence identifications due to availability of accurate masses, retention times, and library spectra for comparison. Utilizing the spectra of these microcystins, relatively high-abundance diagnostic product-ions were identified and employed to screen the data for additional candidate microcystins. Microcystins without a standard that had an exact mass matching a microcystin published in CyanoMetDB were considered semi-known-unknown microcystins. The remaining microcystins were considered unknown-unknown microcystins. The identities of the microcystins determined herein were additionally supported by product-ion analysis, thiol reactivity, esterification reactions, neutral loss analysis, and literature contextualization.
In total, utilizing the systematic workflow presented herein, 23 microcystins were identified in the M. aeruginosa culture, including two not published previously: [d-Asp]MC-LCit and the incompletely identified MC-L(CHNO).
微囊藻毒素是一个新出现的公共卫生问题。这些毒素是有害蓝藻水华的次生代谢物,随着水体富营养化,水华变得更加普遍。暴露于微囊藻毒素会导致疾病、肝损伤,甚至死亡。迄今为止,已鉴定出超过 300 种微囊藻毒素,其毒性因特定氨基酸组成的不同而有所差异。由于微囊藻毒素的这种多样性,以及检测到尚未发现的微囊藻毒素的可能性,建立一种方法学工作流程来识别复杂样品中的任何微囊藻毒素是至关重要的,无论是否有参考标准。此外,对这些鉴定赋予不同程度的置信度对于有效地传达发现结果至关重要。
利用液相色谱-高分辨质谱法鉴定来自铜绿微囊藻和鱼腥藻的蓝藻提取物中的微囊藻毒素。首先,在蓝藻提取物中鉴定出具有标准品的微囊藻毒素同系物。由于存在准确的质量、保留时间和库谱可供比较,这些已知-未知微囊藻毒素被认为是具有最高置信度的鉴定结果。利用这些微囊藻毒素的谱图,鉴定出相对高丰度的诊断产物离子,并将其用于筛选数据中其他候选微囊藻毒素。没有标准品但精确质量与 CyanoMetDB 中发表的微囊藻毒素相匹配的微囊藻毒素被认为是半已知-未知微囊藻毒素。其余的微囊藻毒素被认为是未知-未知微囊藻毒素。本文确定的微囊藻毒素的身份还得到了产物离子分析、巯基反应性、酯化反应、中性丢失分析和文献背景的支持。
总共,利用本文提出的系统工作流程,在铜绿微囊藻培养物中鉴定出 23 种微囊藻毒素,其中包括两种以前未发表的:[d-Asp]MC-LCit 和不完全鉴定的 MC-L(CHNO)。