Movatterモバイル変換


[0]ホーム

URL:


Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
Thehttps:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

NIH NLM Logo
Log inShow account info
Access keysNCBI HomepageMyNCBI HomepageMain ContentMain Navigation
pubmed logo
Advanced Clipboard
User Guide

Full text links

Frontiers Media SA full text link Frontiers Media SA Free PMC article
Full text links

Actions

.2020 Jun 17:11:1201.
doi: 10.3389/fmicb.2020.01201. eCollection 2020.

Oxidative Stress, Programmed Cell Death and Microcystin Release inMicrocystis aeruginosa in Response toDaphnia Grazers

Affiliations

Oxidative Stress, Programmed Cell Death and Microcystin Release inMicrocystis aeruginosa in Response toDaphnia Grazers

Piotr Rzymski et al. Front Microbiol..

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.

PubMed Disclaimer

Figures

Figure 1
Figure 1
The growth (mean and SD) ofMicrocystis aeruginosa exposed for 7 days to different concentrations ofDaphnia magna(A) andDaphnia cucullata(B) (n = 5). An asterisk indicates a significant difference with the control (p < 0.05; Mann-Whitney U test).
Figure 2
Figure 2
The intracellular reactive oxygen species (ROS) level (mean and SD) ofM. aeruginosa exposed for 7 days to different concentrations ofD. magna(A) andD. cucullata(B) (n = 5). An asterisk indicates a significant difference with the control (p < 0.05; Mann-Whitney U test).
Figure 3
Figure 3
The peroxidation of lipids measured by means of intracellular thiobarbituric acid reactive substance content (mean and SD), mainly represented by malondialdehyde (MDA) inM. aeruginosa exposed for 7 days to different concentrations ofD. magna andD. cucullata (n = 5). An asterisk indicates a significant difference with the control (p < 0.05; Mann-Whitney U test).
Figure 4
Figure 4
The caspase-3-like activity (mean and SD), a marker of PCD, inM. aeruginosa exposed for 7 days to different concentrations ofD. magna(A) andD. cucullata(B) (n = 5). Different letters indicate statistically significant differences between studied groups for each time interval (p < 0.05;post-hoc Dunn’s test following Kruskal-Wallis ANOVA).
Figure 5
Figure 5
The extracellular concentration (mean and SD) of microcystin-LR(A) and level of bound exopolysaccharide (EPS) fraction(B) inM. aeruginosa exposed for 7 days to different concentrations ofD. magna andD. cucullata (n = 5). An asterisk indicates a significant difference with the control (p < 0.05; Mann-Whitney U test).
See this image and copyright information in PMC

References

    1. Asplund-Samuelsson J., Bergman B., Larsson J. (2012). Prokaryotic caspase homologs: phylogenetic patterns and functional characteristics reveal considerable diversity. PLoS One 7:e49888. 10.1371/journal.pone.0049888, PMID: - DOI - PMC - PubMed
    1. Asselman J., De Coninck D. I. M., Beert E., Janssen C. R., Orsini L., Pfrender M. E., et al. (2017). Bisulfite sequencing with Daphnia highlights a role for epigenetics in regulating stress response to Microcystis through preferential differential methylation of serine and threonine amino acids. Environ. Sci. Technol. 51, 924–931. 10.1021/acs.est.6b03870 - DOI - PubMed
    1. Ayala A., Muñoz M. F., Argüelles S. (2014). Lipid peroxidation: production, metabolism, and signaling mechanisms of malondialdehyde and 4-hydroxy-2-nonenal. Oxidative Med. Cell. Longev. 2014, 360438–360438. 10.1155/2014/360438, PMID: - DOI - PMC - PubMed
    1. Bidle K. D. (2016). Programmed cell death in unicellular phytoplankton. Curr. Biol. 26, R594–R607. 10.1016/j.cub.2016.05.056, PMID: - DOI - PubMed
    1. Bojadzija Savic G., Bormans M., Edwards C., Lawton L., Briand E., Wiegand C. (2020). Cross talk: two way allelopathic interactions between toxic Microcystis and Daphnia. Harmful Algae 94:101803. 10.1016/j.hal.2020.101803 - DOI - PubMed

LinkOut - more resources

Full text links
Frontiers Media SA full text link Frontiers Media SA Free PMC article
Cite
Send To

NCBI Literature Resources

MeSHPMCBookshelfDisclaimer

The PubMed wordmark and PubMed logo are registered trademarks of the U.S. Department of Health and Human Services (HHS). Unauthorized use of these marks is strictly prohibited.


[8]ページ先頭

©2009-2025 Movatter.jp