Abstract
Cyanobacteria are considered a rich source of secondary metabolites with potential biotechnological applications. Additionally, they have the capability to produce some potent toxins (cyanotoxins) that can have consequences for both environmental and human health. This group of microorganisms with a long evolutionary history and a remarkable adaptability can be found both in aquatic and terrestrial ecosystems, including extreme environments (e.g., freshwater, marine, terrestrial, hot springs, deserts, etc.). Cyanotoxins can be classified into five functional groups according to their primary target organ or effects being designated as hepatotoxins, neurotoxins, cytotoxins, dermatotoxins, and irritant toxins. In this work, the presence of genes involved in the biosynthesis of cyanotoxins (microcystin, saxitoxin, cylindrospermopsin, and anatoxin) were screened from more than 200 strains of cyanobacteria. The isolates were obtained from different samples along the Moroccan Atlantic coast (several sampling sites from El Jadida to Essaouira), and from an ancient Portuguese cistern located at El Jadida. There is a gap in the literature regarding the presence of cyanotoxins in this region and some of the isolated strains are related to genera (e.g., Phormidium sp., Pseudanabaena sp., Leptolyngbya sp., Lyngbya sp., and Geitlerinema sp.) that have been reported as potential cyanotoxins producers. Future work will include detection by liquid chromatography–mass spectrometry (LC-MS) to confirm the production of cyanotoxins. Furthermore, the isolates will be deposited in our in-house culture collection (LEGE-CC), and will be available for future studies, increasing the size and diversity of the collection.
Author Contributions
Conceptualization, J.M.; methodology, R.S., J.M. and F.O.; validation, J.M., B.S. and V.V.; investigation, R.S., J.M., F.O., B.S. and V.V.; resources, V.V.; data curation, R.S., J.M. and F.O.; writing—original draft preparation, R.S.; writing—review and editing, J.M., F.O. and V.V.; supervision, J.M. and V.V.; funding acquisition, V.V. All authors have read and agreed to the published version of the manuscript.
Funding
This research was financed by IS_MIRRI21 project and the funding from the European Union’s Horizon 2020 Research and innovation programme under the grant agreement No 871129. The project EMERTOX has received funding from the European Union’s Horizon 2020 Marie Skłodowska-Curie Research and Innovation Staff Exchange, under grant agreement No 78069.
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
Not applicable.
Conflicts of Interest
The authors declare no conflict of interest.
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