In Vitro Toxicological Screening of Stable and Senescing Cultures of Aphanizomenon, Planktothrix, and Raphidiopsis
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Published on: December 8, 2017
Łukasz Wejnerowski1, Halina Falfushynska2, Oksana Horyn2
1Department of Hydrobiology, Institute of Environmental Biology, Faculty of Biology, Adam Mickiewicz University in Poznań, Uniwersytetu Poznańskiego 6, 61-614 Poznań, Poland.
Abstract:
Toxicity of cyanobacteria is the subject of ongoing research, and a number of toxic metabolites have been described, their biosynthesis pathways have been elucidated, and the mechanism of their action has been established. However, several knowledge gaps still exist, e.g., some strains produce hitherto unknown toxic compounds, while the exact dynamics of exerted toxicity during cyanobacterial growth still requires further exploration. Therefore, the present study investigated the toxicity of extracts of nine freshwater strains of Aphanizomenon gracile, an Aphanizomenon sp. strain isolated from the Baltic Sea, a freshwater strain of Planktothrix agardhii, and two strains of Raphidiopsis raciborskii obtained from 25- and 70-day-old cultures. An in vitro experimental model based on Cyprinus carpio hepatocytes (oxidative stress markers, DNA fragmentation, and serine/threonine protein activity) and brain homogenate (cholinesterase activity) was employed. The studied extracts demonstrated toxicity to fish cells, and in general, all examined extracts altered at least one or more of considered parameters, indicating that they possess, to some degree, toxic potency. Although the time from which the extracts were obtained had a significant importance for the response of fish cells, we observed strong variability between the different strains and species. In some strains, extracts that originated from 25-day-old cultures triggered more harmful effects on fish cells compared to those obtained from 70-day-old cultures, whereas in other strains, we observed the opposite effect or a lack of a significant change. Our study revealed that there was no clear or common pattern regarding the degree of cyanobacterial bloom toxicity at a given stage of development. This means that young cyanobacterial blooms that are just forming can pose an equally toxic threat to aquatic vertebrates and ecosystem functioning as those that are stable or old with a tendency to collapse. This might be largely due to a high variability of strains in the bloom.
Insights
Cyanobacterial bloom toxicity varies greatly between strains and growth stages. Young and old blooms can pose equal threats to aquatic life due to high strain variability.
Area of Science:
- Environmental Science
- Aquatic Toxicology
- Microbiology
Background:
- Cyanobacterial toxins pose risks, but knowledge gaps remain regarding unknown compounds and toxicity dynamics during growth.
- Understanding cyanotoxin variability is crucial for assessing ecological and health impacts.
Purpose of the Study:
- Investigate the toxicity of various cyanobacterial strains (Aphanizomenon gracile, Aphanizomenon sp., Planktothrix agardhii, Raphidiopsis raciborskii) at different culture ages.
- Evaluate the impact of cyanobacterial extracts on fish cell health using in vitro models.
Main Methods:
- Utilized an in vitro model with Cyprinus carpio hepatocytes and brain homogenate.
- Assessed oxidative stress markers, DNA fragmentation, serine/threonine protein activity, and cholinesterase activity.
Main Results:
- All tested cyanobacterial extracts exhibited toxicity to fish cells, altering key biological parameters.
- Toxicity varied significantly between strains and species, and was influenced by culture age (25 vs. 70 days).
- No consistent pattern emerged linking bloom age to toxicity levels, with young blooms showing comparable risks to older ones.
Conclusions:
- Cyanobacterial bloom toxicity is highly strain-dependent and not predictable by bloom age alone.
- Both young and mature cyanobacterial blooms can present significant toxicological risks to aquatic ecosystems.
- Further research is needed to understand the complex interactions driving cyanotoxin variability and impact.

