Microcystis aeruginosa and Raphidiopsis raciborskii (previously Cylindrospermopsis raciborskii) are both common bloom-forming cyanobacteria which can coexist but alternatively dominate in freshwater ecosystems. To predict their blooming dynamics, we need to understand the potential environmental factors determining their succession. In the present study, we examined the pairwise competition of the three M. aeruginosa strains (FACHB905, 469 and 915) with one R. raciborskii strain (N8) at three temperature levels (16 °C, 24 °C, and 32 °C). We found that the competitive ability of three Microcystis strains were highly variable. M. aeruginosa FACHB905 was the strongest competitor among them which can finally exclude R. raciborskii N8 regardless of initial biovolume ratios and temperature levels. The competitive exclusion of N8 by 915 also was observed at 24 °C, but they coexisted at 16 °C and 32 °C. We observed that M. aeruginosa FACHB469 and R. raciborskii N8 were able to coexist under all the temperature levels, and M. aeruginosa FACHB469 was the weakest competitor among the three M. aeruginosa strains. Rates of competitive exclusion (RCE) showed that temperature affects the competition between three M. aeruginosa strains and R. raciborskii N8. M. aeruginosa strains always grew quickly at 24 °C and significantly enlarged its dominance in the co-culture system, while R. raciborskii N8 was able to maintain its initial advantages at both 16 and 32 °C. The competitive advantage of M. aeruginosa FACHB905 may be explained by allelopathic interactions through its allelochemicals and other secondary metabolites other than microcystin. We concluded that both strain difference and temperature can affect the competition between M. aeruginosa and R. raciborskii. Our results highlighted the complexity of cyanobacterial dynamics in waterbodies where there exist multiple strains.

Microbial degradation is an important route for removing environmental microcystins (MCs). Here, we investigated the ecological distribution of microcystin degraders (mlr-genotype), and the relationship between the substrate specificity of the microcystin degrader and the profile of microcystin congener production in the habitat. We showed that microcystin degraders were widely distributed and closely associated with Microcystis abundance in Lake Taihu, China. We characterized an indigenous degrader, Sphingopyxis N5 in the northern Lake Taihu, and it metabolized six microcystin congeners in increasing order (RR > LR > YR > LA > LF and LW). Such a substrate-specificity pattern was congruent to the order of the dominance levels of these congeners in northern Lake Taihu. Furthermore, a meta-analysis on global microcystin degraders revealed that the substrate-specificity patterns varied geographically, but generally matched the profiles of microcystin congener production in the degrader habitats, and the indigenous degrader typically metabolized well the dominant MC congeners, but not the rare congeners in the habitat. This highlighted the phenotypic congruence between microcystin production and degradation in natural environments. We theorize that such congruence resulted from the metabolic adaptation of the indigenous degrader to the local microcystin congeners. Under the nutrient microcystin selection, the degraders might have evolved to better exploit the locally dominant congeners. This study provided the novel insight into the ecological distribution and adaptive degradation of microcystin degraders.

Cylindrospermopsin (CYN) is a cyanotoxin that is of particular concern for its potential toxicity to human and animal health and ecological consequences due to contamination of drinking water. The increasing emergence of CYN around the world has led to urgent development of rapid and high-throughput methods for its detection in water. In this study, a highly sensitive monoclonal antibody N8 was produced and characterized for CYN detection through the development of a direct competitive time-resolved fluorescence immunoassay (TRFIA). The newly developed TRFIA exhibited a typical sigmoidal response for CYN at concentrations of 0.01–100 ng mL⁻¹, with a wide quantitative range between 0.1 and 50 ng mL⁻¹. The detection limit of the method was calculated to be 0.02 ng mL⁻¹, which is well below the guideline value of 1 μg L⁻¹ and is sensitive enough to provide an early warning of the occurrence of CYN-producing cyanobacterial blooms. The newly developed TRFIA also displayed good precision and accuracy, as evidenced by low coefficients of variation (4.1–6.5%). Recoveries ranging from 92.6% to 108.8% were observed upon the analysis of CYN-spiked water samples. Moreover, comparison of the TRIFA with an ELISA kit through testing 76 water samples and 15 Cylindrospermopsis cultures yielded a correlation r² value of 0.963, implying that the novel immunoassay was reliable for the detection of CYN in water and algal samples.

Cyanobacterial bloom is one of the most urgent global environmental issues, which eventually could threaten human health and safety. Sonication treatment (ST) is a potential effective method to control cyanobacteria blooms in the field. Currently, the bottleneck of extensive application of ST is the difficulty to estimate the ST effect on the cyanobacterial cells and then determine suitable ST times in the field. In this study, cyanobacterial Microcystis samples sonicated at different times were first measured by a spectrophotometer to calculate the removal efficiency of Microcystis cells. Additionally, they were observed by TEM to reveal the intracellular structure changes of the cells. Then the samples were measured by an experimental setup based on polarized light scattering to measure the polarization parameters. Experimental results indicated that the polarization parameters can effectively characterize the intracellular structural changes of Microcystis cells with different ST times, which is quite consistent with the results for removal efficiency and TEM images. Further, the optimal ST time can be inferred by the polarization parameters. These results demonstrate that polarized light scattering can be a potentially powerful tool to explore suitable times for sonication treatment of cyanobacteria blooms.