TY - JOUR
T1 - Chitosan as a Coagulant to Remove Cyanobacteria Can Cause Microcystin Release
AU - Mucci, Maíra
AU - Guedes, Iame A.
AU - Faassen, Elisabeth J.
AU - Lürling, Miquel
PY - 2020/11/10
Y1 - 2020/11/10
N2 - Chitosan has been tested as a coagulant to remove cyanobacterial nuisance. While its coagulation efficiency is well studied, little is known about its effect on the viability of the cyanobacterial cells. This study aimed to test eight strains of the most frequent bloom-forming cyanobacterium, Microcystis aeruginosa, exposed to a realistic concentration range of chitosan used in lake restoration management (0 to 8 mg chitosan L-1). We found that after 1 h of contact with chitosan, in seven of the eight strains tested, photosystem II efficiency was decreased, and after 24 h, all the strains tested were affected. EC50 values varied from 0.47 to > 8 mg chitosan L-1 between the strains, which might be related to the amount of extracellular polymeric substances. Nucleic acid staining (Sytox-Green®) illustrated the loss of membrane integrity in all the strains tested, and subsequent leakage of pigments was observed, as well as the release of intracellular microcystin. Our results indicate that strain variability hampers generalization about species response to chitosan exposure. Hence, when used as a coagulant to manage cyanobacterial nuisance, chitosan should be first tested on the natural site-specific biota on cyanobacteria removal efficiency, as well as on cell integrity aspects.
AB - Chitosan has been tested as a coagulant to remove cyanobacterial nuisance. While its coagulation efficiency is well studied, little is known about its effect on the viability of the cyanobacterial cells. This study aimed to test eight strains of the most frequent bloom-forming cyanobacterium, Microcystis aeruginosa, exposed to a realistic concentration range of chitosan used in lake restoration management (0 to 8 mg chitosan L-1). We found that after 1 h of contact with chitosan, in seven of the eight strains tested, photosystem II efficiency was decreased, and after 24 h, all the strains tested were affected. EC50 values varied from 0.47 to > 8 mg chitosan L-1 between the strains, which might be related to the amount of extracellular polymeric substances. Nucleic acid staining (Sytox-Green®) illustrated the loss of membrane integrity in all the strains tested, and subsequent leakage of pigments was observed, as well as the release of intracellular microcystin. Our results indicate that strain variability hampers generalization about species response to chitosan exposure. Hence, when used as a coagulant to manage cyanobacterial nuisance, chitosan should be first tested on the natural site-specific biota on cyanobacteria removal efficiency, as well as on cell integrity aspects.
KW - cyanobacteria bloom control
KW - lake restoration
KW - membrane integrity
KW - microcystin
KW - Microcystis aeruginosa
U2 - 10.3390/toxins12110711
DO - 10.3390/toxins12110711
M3 - Article
C2 - 33182627
AN - SCOPUS:85096082981
SN - 2072-6651
VL - 12
JO - Toxins
JF - Toxins
IS - 11
ER -