Oxidative Stress, Programmed Cell Death and Microcystin Release inMicrocystis aeruginosa in Response toDaphnia Grazers
- PMID:32625177
- PMCID: PMC7311652
- DOI: 10.3389/fmicb.2020.01201
Oxidative Stress, Programmed Cell Death and Microcystin Release inMicrocystis aeruginosa in Response toDaphnia Grazers
Abstract
There is increasing evidence that programmed cell death (PCD) in cyanobacteria is triggered by oxidative stress and that it contributes to the survival of the cyanobacterial population such asMicrocystis aeruginosa. At the same time, microcystins (MCs) released during cell lysis have been implicated in colony formation (enabled by the release of polysaccharides) inM. aeruginosa - a strategy that allows the effect of a stressor, including grazing to be avoided or decreased. This experimental research has explored whether extracts ofDaphnia magna andDaphnia cucullata (corresponding to 5, 25, 50, and 100 individuals per liter) reveal the effect on the growth, intracellular reactive oxygen species (ROS) content, lipid peroxidation, PCD, MC-LR release, and bound exopolysaccharide (EPS) level inM. aeruginosa during 7 days of exposure. As demonstrated, extracts of both daphnids induced dose-dependent growth inhibition, increase in ROS levels, lipid peroxidation, and PCD. Moreover, the release of MC-LR and an increase in the bound EPS fraction were observed in treated cultures. Generally, the greatest effects were observed under the influence ofD. magna extracts. The study indicates that grazer presence can potentially trigger a series of events in theMicrocystis population, with cells undergoing oxidative stress-induced PCD associated with MC release, which in turn increases EPS production by intact cells. As argued, this strategy is likely to have evolved in response to abiotic stressors, since both PCD and synthesis of MC in cyanobacteria predate the metazoan lineage. Nevertheless, it may still provide a benefit for the survival of the MC-producingM. aeruginosa population under grazer pressure.
Keywords: Daphnia; Microcystis aeruginosa; cyanobacteria; microcystins; programmed cell death; stress response.
Copyright © 2020 Rzymski, Klimaszyk, Jurczak and Poniedziałek.
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References
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