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. 2025 Feb 22;13(3):486.
doi: 10.3390/microorganisms13030486.

Virus Infection of a Freshwater Cyanobacterium Contributes Significantly to the Release of Toxins Through Cell Lysis

Affiliations

Virus Infection of a Freshwater Cyanobacterium Contributes Significantly to the Release of Toxins Through Cell Lysis

Victoria Lee et al. Microorganisms. .

Abstract

Toxic algal-bloom-forming cyanobacteria are a persistent problem globally for many aquatic environments. Their occurrence is attributed to eutrophication and rising temperatures due to climate change. The result of these blooms is often the loss of biodiversity, economic impacts on tourism and fisheries, and risks to human and animal health. Of emerging interest is the poorly understood interplay between viruses and toxic species that form blooms. This is because recent studies have suggested that viruses may exacerbate the harmful effects of these blooms by contributing to the release of toxins into a dissolved phase upon cell lysis. However, to date, there is no experimental evidence that explicitly implicates viruses in microcystin release. Here, we show experimentally that a virus infection of the toxin-producing, harmful, algal-bloom-forming cyanobacterium Microcystis aeruginosa results in a 4-fold increase in the toxin microcystin-LR two days post-infection (dpi). We also show that the concentrations of microcystin remain high after culture discoloration and host cell lysis. Collectively, our results directly implicate viruses as major contributors to microcystin release from cyanobacteria and emphasize the importance of taking viruses into account in predictive models and in the assessment of water quality and safety.

Keywords: Microcystis aeruginosa; cyanophage; harmful algal bloom; microcystin; virus infection.

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Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Extracellular cyanotoxin release by cyanobacteria such as Microcystis aeruginosa. (A) The measurable extracellular fraction of cyanotoxins in the absence of a virus infection includes toxins that are typically released upon senescence and/or cell death, with some cyanobacterial species being able to release toxins without cell rupture or death. This is what we measured in our control, uninfected M. aeruginosa NIES-298 treatments. (B) The measurable extracellular fraction of cyanotoxins in the presence of viruses includes intracellular toxins that are typically contained within the cyanobacterial cells and are released upon cell lysis. This is what we measured in our virus-infected M. aeruginosa NIES-298 treatments. Created with BioRender.com.
Figure 2
Figure 2
Cyanophage-infected and uninfected M. aeruginosa NIES-298 cyanobacterial cultures and the subsequent analysis of extracellular microcystin-LR dynamics during infection. (a) 1—Cyanobacterial cells were incubated until the late exponential growth phase (i.e., 2.95 ×ばつ 107 cells mL−1); 2—the culture was then split into six replicates at day 0 (dashed line in (b)), three of which were infected with a cyanophage Ma-LMM01 stock that was at a virus particle density of 1.35 ×ばつ 107 mL−1 and three of which were inoculated with an equal volume of a 0.02 μm filtrate of the Ma-LMM01 stock; and 4—ELISA essays and total NIES-298 cell abundance measurements were performed using spectrophotometry and haemocytometry, respectively. (b) M. aeruginosa NIES-298 growth dynamics (n = 3, ±SD) of Ma-LMM01-infected (grey line) and uninfected (green line) treatments up to seven days post-infection on day 0 (indicated as a dashed line). (c) Average (± SD, n = 3) extracellular microcystin-LR concentrations in parts per billion (ppb) in cyanophage Ma-LMM01-infected (dark grey bars) and uninfected (green bars) treatments. ** and * denote significant differences (p < 0.01 and p < 0.05, respectively; ANOVA) between infected and uninfected treatments at individual time points. (d) Average daily rate of extracellular microcystin-LR decrease in infected treatments, calculated between the highest measured concentration on day 2 and the last day of the experiment on day seven. (e) Culture pigmentation (photographed) of a representative triplicate treatment, which was either infected (V) or uninfected (C) by viruses, 0–7 dpi. Panel (a) was created with BioRender.com.

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