Correlation Engine 2.0
Clear Search sequence regions


  • actin (1)
  • aphanizomenon (3)
  • apoptosis (1)
  • Bcl 2 (1)
  • brain (1)
  • cellular (1)
  • cyanobacteria (2)
  • cylindrospermopsin (3)
  • cylindrospermopsis (1)
  • CYP1A (1)
  • CYP26 (1)
  • cyp26b1 (1)
  • cytoskeleton (1)
  • cytoskeleton actin (1)
  • danio rerio (1)
  • dna damage (1)
  • ecosystem (1)
  • EPHX1 (1)
  • european origin (1)
  • FABP1 (1)
  • GADD45 (1)
  • help (1)
  • lipid (2)
  • liver (2)
  • MAPK (1)
  • microcystin- lr (2)
  • microcystins (2)
  • Nrf2 (2)
  • PLA2 (1)
  • PPARa (1)
  • PPM1 (1)
  • PPP6C (1)
  • RAD51 (1)
  • saxitoxins (1)
  • thiol (1)
  • toxins (2)
  • tubulin (2)
  • uracil (2)
  • zebrafish (3)
  • Sizes of these terms reflect their relevance to your search.

    The global increase in cyanobacterial blooms poses environmental and health threats. Selected cyanobacterial strains reveal toxicities despite a lack of synthesis of known toxic metabolites, and the mechanisms of these toxicities are not well understood. Here we investigated the toxicity of non-cylindrospermopsin and non-microcystin producing Aphanizomenon gracile and Raphidiopsis raciborskii of Central European origin to zebrafish exposed for 14 days to their extracts. Toxicological screening revealed the presence of anabaenopeptins and a lack of anatoxin-a, ß-methylamino-L-alanine or saxitoxins in examined extracts. The responses were compared to 20 μg L-1 of common cyanobacterial toxins cylindrospermopsin (CYN) and microcystin-LR (MC-LR). The expression of the marker genes involved in apoptosis (caspase 3a and 3b, Bcl-2, BAX, p53, MAPK, Nrf2), DNA damage detection and repair (GADD45, RAD51, JUN, XPC), detoxification (CYP1A, CYP26, EPHX1), lipid metabolism (PPARa, FABP1, PLA2), phosphorylation/dephosphorylation (PPP6C, PPM1) and cytoskeleton (actin, tubulin) were examined using targeted transcriptomics. Cellular stress and toxicity biomarkers (oxidative injury, antioxidant enzymes, thiol pool status, and lactate dehydrogenase activity) were measured in the liver, and acetylcholinesterase activity was determined as an index of neurotoxicity in the brain. The extracts of three cyanobacterial strains that produce no known cyanotoxins caused marked toxicity in D. rerio, and the biomarker profiles indicate different toxic mechanisms between the bioactive compounds extracted from these strains and the purified cyanotoxins. All studied cyanobacterial extracts and purified cyanotoxins induced oxidative stress and neurotoxicity, downregulated Nrf2 and CYP26B1, disrupted phosphorylation/dephosphorylation processes and actin/tubulin cytoskeleton and upregulated apoptotic activity in the liver. The tested strains and purified toxins displayed distinctively different effects on lipid metabolism. Unlike CYN and MC-LR, the Central European strain of A. gracile and R. raciborskii did not reveal a genotoxic potential. These findings help to further understand the ecotoxicological consequences of toxic cyanobacterial blooms in freshwater ecosystems. Copyright © 2021 Elsevier Ltd. All rights reserved.

    Citation

    Halina Falfushynska, Oksana Horyn, Inna Osypenko, Piotr Rzymski, Łukasz Wejnerowski, Marcin K Dziuba, Inna M Sokolova. Multibiomarker-based assessment of toxicity of central European strains of filamentous cyanobacteria Aphanizomenon gracile and Raphidiopsis raciborskii to zebrafish Danio rerio. Water research. 2021 Apr 15;194:116923

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 33631698

    View Full Text