Multi-detection method for five common microalgal toxins based on the use of microspheres coupled to a flow-cytometry system

• Published in: Analytica chimica acta 2014-11, Vol.850, p.57-64
• Main Authors: Fraga, María, Vilariño, Natalia, Louzao, M. Carmen, Rodríguez, Laura P., Alfonso, Amparo, Campbell, Katrina, Elliott, Christopher T., Taylor, Palmer, Ramos, Vítor, Vasconcelos, Vítor, Botana, Luis M.
• Format: Article
• Language: English
• Subjects: Aquatic toxins; Assaying; Bacterial Toxins; Cyanobacteria - chemistry; Drinking water; Flow Cytometry - methods; Flow-cytometry system; Fresh Water - analysis; Freshwaters; Joining; Kainic Acid - analogs & derivatives; Kainic Acid - analysis; Kainic Acid - isolation & purification; Microalgae - chemistry; Microalgal toxins; Microcystins - analysis; Microcystins - isolation & purification; Microsphere-based array; Microspheres; Multi-detection; Multiplexing; Saxitoxin - analysis; Saxitoxin - isolation & purification; Screening method; Toxins; Tropanes - analysis; Tropanes - isolation & purification; Uracil - analogs & derivatives; Uracil - analysis; Uracil - isolation & purification
• ISSN: 0003-2670; 1873-4324
• DOI: 10.1016/j.aca.2014.08.030

[Display omitted] •Multiplexed method for the detection of five microalgal toxin classes.•Sensitive, easy-to-perform, rapid, semi-quantitative screening technique.•Useful for the detection of freshwater toxins in cyanobacterial samples. Freshwater and brackish microalgal toxins, such as microcystins, cylindrospermopsins, paralytic toxins, anatoxins or other neurotoxins are produced during the overgrowth of certain phytoplankton and benthic cyanobacteria, which includes either prokaryotic or eukaryotic microalgae. Although, further studies are necessary to define the biological role of these toxins, at least some of them are known to be poisonous to humans and wildlife due to their occurrence in these aquatic systems. The World Health Organization (WHO) has established as provisional recommended limit 1μg of microcystin-LR per liter of drinking water. In this work we present a microsphere-based multi-detection method for five classes of freshwater and brackish toxins: microcystin-LR (MC-LR), cylindrospermopsin (CYN), anatoxin-a (ANA-a), saxitoxin (STX) and domoic acid (DA). Five inhibition assays were developed using different binding proteins and microsphere classes coupled to a flow-cytometry Luminex system. Then, assays were combined in one method for the simultaneous detection of the toxins. The IC50's using this method were 1.9±0.1μgL−1 MC-LR, 1.3±0.1μgL−1 CYN, 61±4μgL−1 ANA-a, 5.4±0.4μgL−1 STX and 4.9±0.9μgL−1 DA. Lyophilized cyanobacterial culture samples were extracted using a simple procedure and analyzed by the Luminex method and by UPLC–IT-TOF-MS. Similar quantification was obtained by both methods for all toxins except for ANA-a, whereby the estimated content was lower when using UPLC–IT-TOF-MS. Therefore, this newly developed multiplexed detection method provides a rapid, simple, semi-quantitative screening tool for the simultaneous detection of five environmentally important freshwater and brackish toxins, in buffer and cyanobacterial extracts.