Centre for Environment Fisheries and Aquaculture Science, Barrack Road, Weymouth DT4 8UB, UK.
Biotoxin Metrology, National Research Council Canada, Halifax, NS B3H 3Z1, Canada.
Toxins (Basel). 2022 Dec 30;15(1):27. doi: 10.3390/toxins15010027.
Microcystins and nodularins, produced naturally by certain species of cyanobacteria, have been found to accumulate in aquatic foodstuffs such as fish and shellfish, resulting in a risk to the health of the seafood consumer. Monitoring of toxins in such organisms for risk management purposes requires the availability of certified matrix reference materials to aid method development, validation and routine quality assurance. This study consequently targeted the preparation of a mussel tissue reference material incurred with a range of microcystin analogues and nodularins. Nine targeted analogues were incorporated into the material as confirmed through liquid chromatography with tandem mass spectrometry (LC-MS/MS), with an additional 15 analogues detected using LC coupled to non-targeted high resolution mass spectrometry (LC-HRMS). Toxins in the reference material and additional source tissues were quantified using LC-MS/MS, two different enzyme-linked immunosorbent assay (ELISA) methods and with an oxidative-cleavage method quantifying 3-methoxy-2-methyl-4-phenylbutyric acid (MMPB). Correlations between the concentrations quantified using the different methods were variable, likely relating to differences in assay cross-reactivities and differences in the abilities of each method to detect bound toxins. A consensus concentration of total soluble toxins determined from the four independent test methods was 2425 ± 575 µg/kg wet weight. A mean 43 ± 9% of bound toxins were present in addition to the freely extractable soluble form (57 ± 9%). The reference material produced was homogenous and stable when stored in the freezer for six months without any post-production stabilization applied. Consequently, a cyanotoxin shellfish reference material has been produced which demonstrates the feasibility of developing certified seafood matrix reference materials for a large range of cyanotoxins and could provide a valuable future resource for cyanotoxin risk monitoring, management and mitigation.
微囊藻毒素和节球藻毒素是某些蓝藻物种自然产生的,已被发现会在鱼类和贝类等水生食品中积累,从而对海鲜消费者的健康构成风险。为了进行风险管理,需要对这些生物体中的毒素进行监测,这就需要有经过认证的基质参比物质来辅助方法开发、验证和常规质量保证。因此,本研究的目标是制备一种含有一系列微囊藻毒素类似物和节球藻毒素的贻贝组织参比物质。通过液相色谱-串联质谱(LC-MS/MS)证实,该物质中掺入了 9 种目标类似物,同时还使用 LC 与非靶向高分辨率质谱(LC-HRMS)检测到了 15 种类似物。使用 LC-MS/MS、两种不同的酶联免疫吸附测定(ELISA)方法和定量 3-甲氧基-2-甲基-4-苯基丁酸(MMPB)的氧化裂解方法对参比物质和其他来源组织中的毒素进行定量。不同方法定量的浓度之间相关性各不相同,这可能与测定交叉反应性的差异以及每种方法检测结合毒素的能力有关。从四种独立测试方法确定的总可溶性毒素的共识浓度为 2425 ± 575 µg/kg 湿重。除了可自由提取的可溶性形式(57 ± 9%)之外,还存在 43 ± 9%的结合毒素。在没有进行任何生产后稳定化处理的情况下,将该参比物质储存在冰箱中 6 个月后仍然保持均匀稳定。因此,已经制备出一种含有蓝藻毒素的贝类参比物质,该参比物质证明了为大范围的蓝藻毒素开发经过认证的海鲜基质参比物质的可行性,并且可以为蓝藻毒素风险监测、管理和缓解提供有价值的未来资源。