Cyanobacterial cell-wall components as emerging environmental toxicants - detection and holistic monitoring by cellular signaling biosensors.

Biosensors Cyanobacteria Cyanotoxins Lipopolysaccharide Lipoproteins NFkappaB

Journal

The Science of the total environment
ISSN: 1879-1026
Titre abrégé: Sci Total Environ
Pays: Netherlands
ID NLM: 0330500

Informations de publication

Date de publication:
10 Feb 2022
Historique:
received: 14 07 2021
revised: 04 09 2021
accepted: 24 09 2021
pubmed: 13 10 2021
medline: 24 12 2021
entrez: 12 10 2021
Statut: ppublish

Résumé

Cyanobacterial blooms constitute a recognized danger to aquatic environment and public health not only due to presence of main group of cyanotoxins, such as microcystins, cylindrospermopsin or anatoxin-a, but also other emerging bioactivities. An innovative approach identifying such bioactivities is the application of cellular biosensors based on reporter genes which detect the impact of cyanobacterial cells and components on actual human cells in a physiological-like setting. In the present study biosensor cell lines detecting four different types of bioactivities (ARE - oxidative stress, NFKBRE - immunomodulatory pathogen-associated molecular patterns, AHRE - persistent organic pollutants, GRE - endocrine disruptors) were exposed to concentrated cyanobacterial cells from 21 environmental bloom samples and from eight cultures (Microcystis aeruginosa, Aphanizomenon flos-aquae, Planktothrix agardhii and Raphidiopsis raciborskii). The AHRE and GRE biosensors did not detect any relevant bioactivity. In turn, ARE biosensors were significantly activated by bloom samples from Jeziorsko (180-250%) and Sulejów (250-400%) reservoirs with the highest cyanobacterial biomass, while activation by cultures was weak/undetectable. The same biosensors were stimulated by microcystin-LR (250%) and anatoxin-a (150%). The NFKBRE biosensors were activated to varying extent (140-650%) by most bloom and culture samples, pointing to potential immunomodulatory toxic effects on humans. Lipopolysaccharide and lipoproteins were identified as responsible for NFKBRE activation (probably via pattern recognition receptors), while peptidoglycan had no bioactivity in this assay. Thus, the holistic approach to sample analysis with the application of cellular biosensors geared towards 4 separate pathways/bioactivities was validated for identification of novel bioactivities in organisms with recognized public health significance (e.g. this study is the first to describe cyanobacterial lipoproteins as potential environmental immunomodulators). Moreover, the ability of cellular biosensors to be activated by intact cyanobacterial cells from blooms provides proof of concept of their direct application for environmental monitoring, especially comparison of potential threats without need for chemical analysis and identification of toxicants.

Identifiants

pubmed: 34637876
pii: S0048-9697(21)05723-5
doi: 10.1016/j.scitotenv.2021.150645
pii:
doi:

Substances chimiques

Cyanobacteria Toxins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

150645

Informations de copyright

Copyright © 2021. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of competing interest Authors declare that this research was funded by the National Science Centre, project no. UMO-2012/07/B/NZ8/03991 - “Application of reporter cell biosensors in ecotoxicology of cyanobacteria: new targets for bioactivity” and partly from EEA/Norway Grant Mechanism research grant PL0107 “Cellular biosensors for automated monitoring of environmental pollution”. The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Ilona Gągała-Borowska (I)

European Regional Centre for Ecohydrology of the Polish Academy of Sciences, Tylna 3, 90-364 Lodz, Poland.

Iwona Karwaciak (I)

Laboratory of Transcriptional Regulation, Institute of Medical Biology PAS, Lodowa 106, 93-232 Lodz, Poland.

Dorota Jaros (D)

Laboratory of Transcriptional Regulation, Institute of Medical Biology PAS, Lodowa 106, 93-232 Lodz, Poland; Mabion S.A., Langiewicza 60, 95-050 Konstantynow Lodzki, Poland.

Marcin Ratajewski (M)

Laboratory of Epigenetics, Institute of Medical Biology PAS, Lodowa 106, 93-232 Lodz, Poland.

Mikołaj Kokociński (M)

Department of Hydrobiology, Faculty of Biology, Adam Mickiewicz University, Uniwersytetu Poznańskiego 6, 61-614 Poznan, Poland.

Tomasz Jurczak (T)

UNESCO Chair on Ecohydrology and Applied Ecology, Faculty of Biology and Environmental Protection, University of Lodz, Banacha 12/16, 90-237 Lodz, Poland.

Bartłomiej Remlein (B)

Laboratory of Transcriptional Regulation, Institute of Medical Biology PAS, Lodowa 106, 93-232 Lodz, Poland; Mabion S.A., Langiewicza 60, 95-050 Konstantynow Lodzki, Poland.

Kinga Rudnicka (K)

Laboratory of Transcriptional Regulation, Institute of Medical Biology PAS, Lodowa 106, 93-232 Lodz, Poland; Academya Sp. z o.o., Sienkiewicza 85/87, 90-057 Lodz, Poland.

Łukasz Pułaski (Ł)

Laboratory of Transcriptional Regulation, Institute of Medical Biology PAS, Lodowa 106, 93-232 Lodz, Poland; Department of Molecular Biophysics, Faculty of Biology and Environmental Protection, University of Lodz, Pomorska 141/143, 90-237 Lodz, Poland. Electronic address: lukasz.pulaski@uni.lodz.pl.

Joanna Mankiewicz-Boczek (J)

European Regional Centre for Ecohydrology of the Polish Academy of Sciences, Tylna 3, 90-364 Lodz, Poland. Electronic address: j.mankiewicz@erce.unesco.lodz.pl.

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