Mixture designs to investigate adverse effects upon co-exposure to environmental cyanotoxins. (1st June 2019)

• Record Type: Journal Article
• Authors: Martin, Rubia M.; Stallrich, Jonathan; Bereman, Michael S.
• Is Part Of: Toxicology. Volume 421(2019)
• Page Start: 74
• Page End: 83
• Publication Date: 2019-06-01
• Subjects: HPLC high-performance liquid chromatography -- LC/MS high-pressure liquid chromatography combined mass spectrometry -- IPA ingenuity pathway analysis -- ANOVA analysis of variance -- GO gene ontology -- BMAA β-methylamino-L-alanine -- AEG aminoethyl glycine -- 24DAB 2, 4-diaminobutyric acid -- DEPs differentially expressed proteins; Cyanotoxins -- Mixture design -- Interaction -- Environmental exposure -- Proteomics; Toxicology -- Periodicals; Chemicals -- Physiological effect -- Periodicals; 615.9005
• DOI: 10.1016/j.tox.2019.04.013
• Languages: English
• ISSNs: 0300-483X

Abstract

Graphical abstract: Highlights: Design of experiments (DoE) is a useful method for the characterization of adverse effects caused by exposure to mixtures. Cyanotoxin compounds have the potential to interact with each other. Cyanotoxic mixtures perturb regulation of various canonical pathways, bioprocesses, and upstream regulators. Abstract: The goal of this study was to implement powerful mixture design techniques, commonly used in process optimization, to investigate enhanced adverse effects upon co-exposure to environmental cyanotoxins. Exposure to cyanobacteria, which are found ubiquitously in environmental water reservoirs, have been linked to several neurodegenerative diseases. Despite the known co-occurrence of various cyanotoxins, the majority of studies investigating this link have focused on the investigation of a single cyanotoxin, a noncanonical amino acid called β-methylamino-L-alanine (BMAA), which poorly recapitulates an actual environmental exposure. Interactions amongst cyanotoxic compounds is an area of great concern and remains poorly understood. To this end, we describe the use of a simplex axial mixture design to screen for interactive adverse effects of cyanotoxic mixtures. Using a combination of basic toxicity assays coupled with contemporary proteomic techniques, our results show the existence of a significant (p ≤ 0.01) interaction between BMAA and its isomers aminoethyl glycine (AEG) and 2, 4-diaminobutyric acid (2, 4DAB). Cyanotoxic mixtures significantly decreased cell viability by an average of 19% and increased caspases 3/7 activities by an average of 110% when compared to individual cyanotoxins (p ≤ 0.05). Cyanotoxic mixtures perturbed various biological pathways associated with neurodegeneration, including inhibition of protective autophagy and activation of mitochondrial dysfunction (z-score >|2|). Additionally, exposure to mixtures perturbed important upstream regulators involved in cellular dysfunction, morbidity, and development. Taken together, our results highlight: (1) the need to study combinations of cyanotoxins when investigating the link between cyanobacteria and neurodegenerative pathologies and (2) the application of design of experiment (DoE) as an efficient methodology to study mixtures of relevant environmental toxins.