Effects of the mixotrophic flagellate Ochromonas sp. on colony formation in Microcystis aeruginosa

The aim of this study was to investigate the interactions between the cyanobacteria (Microcystis aeruginosa) and the potential grazer (Ochromonas sp.) with regard to colony formation. Two kinds of treatments were carried out: (i) In the dialyse experiment Microcystis aeruginosa and Ochromonas sp. were physically separated by a dialyse tubing. (ii) In the contact experiment interactions between Microcystis aeruginosa, heterotrophic bacteria and Ochromonas sp. in different concentrations were investigated. In one treatment where the predator Ochromonas sp. came in direct contact with Microcystis, aggregates were formed.In the contact experiment, there were some interactions between the predator Ochromonas sp. and the two groups of prey, Microcystis aeruginosa and heterotrophic bacteria. When exposed to a low initial Ochromonas sp. concentration, Microcystis aeruginosa decreased and then remained stable in concentration. Ochromonas sp. switched to feed on heterotrophic bacteria and increased. At a high initial Ochromonas sp. concentration Microcystis was grazed down.     

Morphological,biochemical and phylogenetic assessments of water‐bloom‐forming tropical morphospecies of Microcystis (Chroococcales,Cyanobacteria)

Previous polyphasic analyses of five morphospecies of the water‐bloom‐forming cyanobacterial genus Microcystis, Microcystis aeruginosa (Kützing) Lemmermann (=Microcystis aeruginosa (Kützing) Kützing), Microcystis ichthyoblabe Kützing, Microcystis novacekii (Komárek) Compère, Microcystis viridis (A. Braun) Lemmermann, and Microcystis wesenbergii (Komárek) Komárek in Kondratieva, have shown them to be conspecific and they have been proposed to be included under the binomial Microcystis aeruginosa (Kützing) Lemmermann. However, several morphospecies from tropical regions, such as Microcystis bengalensis Banerji, Microcystis panniformis Komárek, Komárková‐Legnerová, Sant'anna, Azevedo & Senna, Microcystis protocystis Crow, Microcystis pseudofilamentosa Crow, Microcystis ramosa Bharadwaya, and Microcystis robusta (Clark) Nygaard, have never been analyzed biochemically or phylogenetically; consequently, their taxonomic status is uncertain. To resolve this issue, we collected 57 strains of Microcystis from Vietnam for taxonomic analysis using a polyphasic approach. Strains were assigned to the six tropical morphospecies listed above or to four morphospecies with cosmopolitan distributions (M. aeruginosa, M. ichthyoblabe, M. novacekii, and M. wesenbergii). Several strains produced colony variants in different culture media; some of these variants had forms that overlapped with those of other morphospecies. Cell diameters varied widely between strains (2.6–9.3 µm) and were unrelated to morphospecies discrimination criteria. Strains of the 10 morphospecies examined had similar fatty acid compositions and closely similar 16S rRNA gene sequences (>99.2% similar). Phylogenetic analyses using 16S rRNA gene and 16S–23S internal transcribed spacer sequences did not identify any clear separations corresponding to morphospecies concepts or microcystin‐producing abilities. Thus, the six tropical morphospecies (M. bengalensis, M. panniformis, M. protocystis, M. pseudofilamentosa, M. ramosa, and M. robusta) are not natural taxonomic units within the genus Microcystis and should be included under M. aeruginosa.     

Change in cyanobacterial biovolume due to preservation by Lugol's Iodine

Cyanobacterial biovolume is used as a guide to the public health risk from these organisms for users of potable and recreational waters. Most routine surveillance programs preserve phytoplankton samples before analysis. We tested the effect of Lugol's Iodine, a common preservative, on the cell biovolume of four common freshwater cyanobacteria, Microcystis aeruginosa, Anabaena circinalis, Cylindrospermopsis raciborskii and Aphanocapsa incerta. Linear dimensions and cell area were measured with an image analyser. All four species shrank after preservation. The magnitude of shrinkage varied with species and preservation time but was not affected by Lugol's concentration. The maximum shrinkage in each species was a 30–40% reduction compared to the live cell biovolume. These results suggest shrinkage can be a greater source of uncertainty in estimating the biovolume of toxigenic cyanobacteria in aquatic environments than natural variability in the cell dimensions, instrument precision or cell counting. Standardised cyanobacterial biovolume lists based on agreed geometric shapes and formulae would improve the value of this information for public health risk assessment.     

Cyanobacterial Picoplankton from Lake Constance*

Four types of unicellular cyanobacteria were classified by pigment composition and cell size. These originated from the picoplankton fraction of Lake Constance, Germany. β-Carotene and zeaxanthin were found to be the main carotenoids of three Synechococcus isolates. In this group, coccoid forms with phycocyanin-rich phycobilisomes also produce caloxanthin and nostoxanthin, which are xanthophylls with 3 and 4 hydroxy groups, respectively. In addition, these rare carotenoids are observed in rod-forming Synechococcus isolates which contain phycoerythrin-rich phycobilisomes, but they are very low or absent in the coccoid phycoerythrin-rich isolates. Due to size and pigment content the coccoid forms are similar to Synechococcus leopoliensis (SAUG B 1402-1, formerly Anacystis nidulans) and S. rubescens (SAUG B 3.81) while the rod-forming isolates differ from S. elongatus (PCC 6716) in phycobilisome composition. The isolate BO 8402 was tentatively assigned to Synechocystis but differs in pigment composition from all strains described as yet. The green cultures exhibited a faint red glow due to an unusual high in vivo autofluorescence from phycocyanin. Neither were phycobilisomes found in a standard preparation nor was allophycocyanin present. The most abundant carotenoids are β-carotene and caloxanthin, while zeaxanthin, with 12 % of all colored carotenoids, is low. All forms described in this paper lack complementary chromatic adaptation, indicating that the pigment composition is a reliable parameter to identify these freshwater isolates.     

Effects of Iron on Growth,Pigment Content,Photosystem II Efficiency,and Siderophores Production of <Emphasis Type="Italic">Microcystis aeruginosa</Emphasis> and <Emphasis Type="Italic">Microcystis wesenbergii</Emphasis>

Changes in growth, photosynthetic pigments, and photosystem II (PS II) photochemical efficiency as well as production of siderophores of Microcystis aeruginosa and Microcystis wesenbergii were determined in this experiment. Results showed growths of M. aeruginosa and M. wesenbergii, measured by means of optical density at 665 nm, were severely inhibited under an iron-limited condition, whereas they thrived under an iron-replete condition. The contents of chlorophyll-a, carotenoid, phycocyanin, and allophycocyanin under an iron-limited condition were lower than those under an iron-replete condition, and they all reached maximal contents on day 4 under the iron-limited condition. PS II photochemical efficiencies (maximal PS II quantum yield), saturating light levels (I _k ) and maximal electron transport rates (ETR_max) of M. aeruginosa and M. wesenbergii declined sharply under the iron-limited condition. The PS II photochemical efficiency and ETR_max of M. aeruginosa rose , whereas in the strain of M. wesenbergii, they declined gradually under the iron-replete condition. In addition, I _k of M. aeruginosa and M. wesenbergii under the iron-replete condition did not change obviously. Siderophore production of M. aeruginosa was higher than that of M. wesenbergii under the iron-limited condition. It was concluded that M. aeruginosa requires higher iron concentration for physiological and biochemical processes compared with M. wesenbergii, but its tolerance against too high a concentration of iron is weaker than M. wesenbergii.     

Physicochemical characterization of cyanophage SM-2

Cyanophage SM-2 which infects two unicellular cyanobacteria, Synechococcus elongatus UTEX 563 and Microcystis aeruginosa NRC-1 (Synechococcus sp. NRC-1) UTEX 1937 has a buoyant density of 1.483 g/cm³, a DNA buoyant density of 1.729 g/cm³ and a guanine + cytosine (G+C) content of 69–70%. The protein patterns of cyanophage SM-2 particles showed 11 bands, as determined by polyacrylamide gel electrophoresis, with the bulk of the protein mass concentrated at the 39,000 Mr band. There appear to be no cross-reacting anibodies to whole virus particles of cyanophages SM-1, SM-2 and AS-1. Cyanophage SM-2 requires the presence of cations for viral stability.     

Effects of photosynthetic inhibitors and light-dark regimes on the replication of cyanophage SM-2

The effects of photosynthetic inhibitors and light-dark regimes on the replication of cyanophage SM-2 in its host cyanobacteria (Synechococcus elongatus UTEX 563 and Microcystis aeruginosa NRC-1, Synechococcus NRC-1 UTEX 1937) have been investigated. Photoassimilation of CO₂ by infected cells was enhanced and remained elevated until late in the infection cycle. Photosynthetic inhibitors and the removal of light suppressed viral replication. SM-2, like other cyanophage of unicellular cyanobacteria, is highly dependent on host photosynthetic metabolism for the energy required in replication.Abbreviations DCMU 3-(3,4-dichlorophenyl)-1,1-dimethylurea - CCCP carbonyl-cyanide m-chlorophenyl hydrazone - MMH Modified Modified Hughes Medium     

A comparison of the carotenoids of strains of Oscillatoria and Spirulina (Cyanobacteria)

The qualitative and quantitative carotenoid composition is reported for (i) a red and a green strain of Oscillatoria limnetica and a green strain of Spirulina platensis cultivated under identical conditions and (ii) a red and a green strain of Spirulina subsalsa grown under identical conditions. No correlation between colour and carotenoid content was obtained. However, differences in carotenoid composition within the Oscillatoria and Spirulina strains were observed. Both oscillol diglycoside ex Oscillatoria limnetica and myxol glycoside ex Spirulina platensis were mixed α-glycosides with chinovose-fucose present in ca 7:2 ratio. Analytical procedures are given. The chemosystematic implications for the current taxonomy of the genera Oscillatoria and Spirulina are discussed.     

Effects of nitrogen on interspecific competition between two cell-size cyanobacteria: Microcystis aeruginosa and Synechococcus sp.

Micro-cyanobacteria and pico-cyanobacteria coexist in many lakes throughout the world. Their distinct cell sizes and nutrient utilization strategies may lead to dominance of one over the other at varying nutrient levels. In this study, Microcystis aeruginosa and Synechococcus sp. were chosen as representative organisms of micro- and pico-cyanobacteria, respectively. A series of nitrate and ammonia conditions (0.02, 0.1, 0.5, and 2.5 mg N L⁻¹) were designed in mono- or co-cultured systems, respectively. Growth rates of the two species were calculated and fitted by the Monod and Logistic equations. Furthermore, the interspecific competition was analyzed using the Lotka–Volterra model. In mono-cultures, the two cyanobacteria displayed faster growth rates in ammonia than in nitrate. Meanwhile, Synechococcus sp. showed faster growth rates compared to M. aeruginosa in lower N groups (≤ 0.5 mg N L⁻¹). However, in the highest nitrate treatment (2.5 mg N L⁻¹), M. aeruginosa achieved much higher biomass and faster growth rates than Synechococcus sp.. In co-cultures, Synechococcus sp. dominated in the lowest N treatment (0.02 mg N L⁻¹), but M. aeruginosa dominated under the highest nitrate condition (2.5 mg N L⁻¹). Based on the analysis of Raman spectra of living cells in mono-cultures, nitrate (2.5 mg N L⁻¹) upgraded the pigmentary contents of M. aeruginosa better than ammonia (2.5 mg N L⁻¹), but nitrogen in different forms showed little effects on the pigments of Synechococcus sp.. Findings from this study can provide valuable information to predict cyanobacterial community succession and aquatic ecosystem stability.     

Inhibition of Chlorella growth by the lipids of cyanobacterium Microcystis aeruginosa

The total lipids of the cyanobacterium Microcystis aeruginosa have been isolated and fractionated into its components. Of these lipid components, only the fatty acid-containing fraction inhibited the growth of the green alga Chlorella pyrenoidosa. The inhibitory activity appears to be due to linoleic and linolenic acids, which are both present in significants quantities. These acids may be the substances responsible for the reported toxicity of Microcystis aeruginosa to Chlorella.     

TOXIN EXTRACTION FROM THE BLUE-GREEN ALGA MICROCYSTIS AERUGINOSA BY DIFFERENT EXTRACTION MEDIA

SUMMARY

The extractability of toxin from Microcystis aeruginosa isolate UV-006 by different extraction media such as O, 1N HC1, 2N CH₃COOH, Triton X-100 and water at different pH levels was investigated. The best recovery of toxin was achieved with water at a pH of 10 while the recoveries with the more acidic media tended to be lower.     

Spatio‐temporal distribution of phytoplankton in four coastal rivers of southeastern of Ivory Coast (Soumié, Eholié, Ehania and Noé)

Spatio‐temporal dynamics of phytoplankton and their relation to abiotic environmental factors in four rivers of south‐eastern Ivory Coast (Soumié, Eholié, Ehania and Noé) was analysed from July 2003 to March 2005. The pelagic zone of each river was sampled upstream and downstream. Phytoplankton abundance was higher in Noé River (154.3 10⁴ cells l^?1) and lower in Eholié river (23.05 10⁴ cells l^?1). Dominant taxa were Microcystis aeruginosa (Kütz.) Lemmerm. and Aphanocapsa incerta (Lemmerm.) Cronberg & Komárek. In general, minimum densities of phytoplankton were observed during the rainy season, while maximum were observed in dry season in the whole stations of the rivers studied, such periods corresponding to low and high concentrations of nitrates. Among the rivers surveyed, Eholié river seems to be the least disturbed because of its higher species diversity. Seasonality fluctuations of algae abundance appear to be influenced by the flow of water and nitrate levels. This work is a useful starting point for future research on micro algae in Ivory Coast.     

DIGESTION OF MICROCYSTIS AERUGINOSA BY OREOCHROMIS MOSSAMBICUS

SUMMARY

The mean assimilation efficiency of aquarium acclimatized Oreochromis mossambiaue fed on a diet of Microcystis aeruginosa collected from Hartbeespoort Dam was determined as 50,8% for total organic matter, 63,7% for protein and 75,5% for phosphorus. Transmission electron microscopic examination of faeces of fish fed on M. aeruginosa, revealed that most Microcystis cell walls had become permeable allowing cell contents to leach out. Further digestion resulted in the break down of the cell wall structure. Up to 25% of the cells, however, appeared intact after passing through the fish. Fish fed on a diet of M. aeruginosa lost mass initially, but after 21 days showed a slight gain in mass. The high protein content of M. aeruginosa nay have inhibited efficient metabolism and would have led to reduced growth in fish.     

巢湖铜绿微囊藻Chao 1910的基因组学和磷代谢通路分析

【背景】铜绿微囊藻(Microcystis aeruginosa)广泛分布于温带湖泊,因产生微囊藻毒素且易成为蓝藻水华优势藻株而备受关注。【目的】基于全基因组序列分析和基因转录水平验证,阐明从巢湖新分离的铜绿微囊藻Chao 1910的主要代谢通路和磷营养高效利用机制。【方法】通过第三代测序技术拼接获得Chao1910的全基因组序列,完成主要代谢通路的基因注释,并对与蓝藻水华优势藻株形成相关的磷代谢通路进行深入分析。【结果】比较基因组学表明,Chao1910藻株与日本铜绿微囊藻NIES-843的亲缘关系最近,其糖酵解、磷酸戊糖途径和核苷酸合成等代谢通路的基因组成非常保守,同时具有完整的磷转运、磷吸收、多聚磷酸盐合成/分解等磷营养高效利用的通路。不同于其他铜绿微囊藻,Chao 1910藻株不具有微囊藻毒素合成基因簇,推测其主要依靠对磷营养的高效利用获取生存竞争优势。【结论】Chao1910藻株是巢湖首株完成全基因组测序的铜绿微囊藻,这将有助于揭示其获得生存竞争优势的分子机制,为遏制巢湖蓝藻水华暴发提供依据。     

A relationship between Pseudomonal growth behaviour and cystic fibrosis patient lung function identified in a metabolomic investigation

Chronic polymicrobial lung infections in adult cystic fibrosis patients are typically dominated by high levels of Pseudomonas aeruginosa. Determining the impact of P. aeruginosa growth on airway secretion composition is fundamental to understanding both the behaviour of this pathogen in vivo, and its relationship with other potential colonising species. We hypothesised that the marked differences in the phenotypes of clinical isolates would be reflected in the metabolite composition of spent culture media. ¹H NMR spectroscopy was used to characterise the impact of P. aeruginosa growth on a synthetic medium as part of an in vitro CF lower airways model system. Comparisons of 15 CF clinical isolates were made and four distinct metabolomic clusters identified. Highly significant relationships between P. aeruginosa isolate cluster membership and both patient lung function (FEV₁) and spent culture pH were identified. This link between clinical isolate growth behaviour and FEV₁ indicates characterisation of P. aeruginosa growth may find application in predicting patient lung function while the significant divergence in metabolite production and consumption observed between CF clinical isolates suggests dominant isolate characteristics have the potential to play both a selective role in microbiota composition and influence pseudomonal behaviour in vivo.     

Grazing on toxic and non-toxic Microcystis aeruginosa PCC7820 by Unio douglasiae and Corbicula fluminea

To explore the potential grazing effects of mussels on Microcystis aeruginosa, a common bloom-forming phytoplankton, Unio douglasiae and Corbicula fluminea were fed with Scenedesmus obliquus, toxic and non-toxic strains of Microcystis aeruginosa as single food and as mixtures in the laboratory. When fed with single foods, U. douglasiae has similar clearance rates on the three algae populations, while C. fluminea has significantly lower clearance rate on toxic M. aeruginosa than those on the other two algae populations. When fed with mixture foods, both the mussels show significantly higher clearance rates than on single foods. The clearance rates of U. douglasiae on the different food mixtures are not significantly different, and C. fluminea has a significantly lower clearance rate on the toxic food mixtures than that on non-toxic food mixtures. Although the relative lower clearance rates of C. fluminea on toxic food, we may still deduce that both the mussels can exert grazing pressure on phytoplankton. The deduction is supported by the composition of the excretion products. The excretion products (faeces and pseudofaeces) of both mussels contained mainly S. obliquus. In both mixed-food treatments, the ratios of S. obliquus to M. aeruginosa in the excrete products are significantly higher than those in the foods. Therefore, it can be concluded that both mussels prefer M. aeruginosa to S. obliquus, and can cause grazing pressure on M. aeruginosa.     

A freshwater bacterial strain,Shewanella sp. Lzh-2, isolated from Lake Taihu and its two algicidal active substances,hexahydropyrrolo[1,2-a]pyrazine-1,4-dione and 2, 3-indolinedione

Cyanobacterial blooms have become a serious problem in Lake Taihu during the last 20 years, and Microcystis aeruginosa and Synechococcus sp. are the two dominant species in cyanobacterial blooms of Lake Taihu. A freshwater bacterial strain, Shewanella sp. Lzh-2, with strong algicidal properties against harmful cyanobacteria was isolated from Lake Taihu. Two substances with algicidal activity secreted extracellularly by Shewanella sp. Lzh-2, S-2A and S-2B, were purified from the bacterial culture of strain Lzh-2 using ethyl acetate extraction, column chromatography, and high performance liquid chromatography (HPLC) in turn. The substances S-2A and S-2B were identified as hexahydropyrrolo[1,2-a]pyrazine-1,4-dione and 2, 3-indolinedione (isatin), respectively, based on liquid chromatography-mass spectrometry (LC-MS), gas chromatography-mass spectrometry (GC-MS), and hydrogen-nuclear magnetic resonance (H-NMR) analyses, making this the first report of their algicidal activity toward cyanobacteria. S-2A (hexahydropyrrolo[1,2-a]pyrazine-1,4-dione) had no algicidal effects against Synechococcus sp. BN60, but had a high level of algicidal activity against M. aeruginosa 9110. The LD50 value of S-2A against M. aeruginosa 9110 was 5.7 μg/ml. S-2B (2, 3-indolinedione) showed a potent algicidal effect against both M. aeruginosa 9110 and Synechococcus sp. BN60, and the LD50 value of S-2B against M. aeruginosa 9110 and Synechococcus sp. BN60 was 12.5 and 34.2 μg/ml, respectively. Obvious morphological changes in M. aeruginosa 9110 and Synechococcus sp. BN60 were observed after they were exposed to S-2A (or S-2B) for 24 h. Approximately, the algicidal activity, the concentration of S-2A and S-2B, and the cell density of Lzh-2 were positively related to each other during the cocultivation process. Overall, these findings increase our knowledge about algicidal substances secreted by algicidal bacteria and indicate that strain Lzh-2 and its two algicidal substances have the potential for use as a bio-agent in controlling cyanobacterial blooms in Lake Taihu.     

Plasmid distribution among unicellular and filamentous toxic cyanobacteria

Plasmid content of 5 hepatotoxin and 2 neurotoxin producing cyanobacterial strains were analyzed. Among the hepatotoxin-producing strains, Microcystis aeruginosa PCC7820, M. aeruginosa M228 and M. aeruginosa UV027 were found to carry plasmids, whereas other hepatotoxin and neurotoxin producing strains did not harbor any plasmids. Correlations were sought between toxicity and the presence of plasmids in toxic cyanobacteria as a function of age. Aged cultures of M. aeruginosa PCC7820 exhibited toxicity and harbored plasmids. In other cyanobacterial strains, plasmids were not detected. The data add to and support the current understanding that plasmids are probably not involved in toxin production in cyanobacteria.Author for Correspondence     

Evolutionary Changes in Growth Rate and Toxin Production in the Cyanobacterium <Emphasis Type="Italic">Microcystis aeruginosa</Emphasis> Under a Scenario of Eutrophication and Temperature Increase

Toxic blooms of the cyanobacterium Microcystis aeruginosa affect humans and animals in inland water systems worldwide, and it has been hypothesized that the development of these blooms will increase under the future scenario of global change, considering eutrophication and temperature increase as two important consequences. The importance of genetic adaptation, chance and history on evolution of growth rate, and toxin production of M. aeruginosa was studied under these new conditions. The experiment followed the idea of “replaying life’s tape” by means of the simultaneous propagation of 15 independent isolates of three M. aeruginosa strains, which were grown under doubled nutrient concentration and temperature during c. 87 generations. Adaptation by new mutations that resulted in the enhancement of growth rate arose during propagation of derived cultures under the new environmental conditions was the main component of evolution; however, chance also contributed in a lesser extension to evolution of growth rate. Mutations were selected, displacing the wild-type ancestral genotypes. In contrast, the effect of selection on mutations affecting microcystin production was neutral. Chance and history were the pacemakers in evolution of toxin production. Although this study might be considered an oversimplification of the reality, it suggest that a future scenario of global change might lead to an increase in M. aeruginosa bloom frequency, but no predictions about the frequency of toxicity can be made.     

Growth characteristics and growth modeling of <Emphasis Type="Italic">Microcystis aeruginosa</Emphasis> and <Emphasis Type="Italic">Planktothrix agardhii</Emphasis> under iron limitation

Although iron is a key nutrient for algal growth just as are nitrogen and phosphorus in aquatic systems, the effects of iron on algal growth are not well understood. The growth characteristics of two species of cyanobacteria, Microcystis aeruginosa and Planktothrix agardhii, in iron-limited continuous cultures were investigated. The relationships between dissolved iron concentration, cell quota of iron, and population growth rate were determined applying two equations, Monod’s and Droop’s equations. Both species produced hydroxamate-type siderophores, but neither species produced catechol-type siderophores. The cell quota of nitrogen for both M. aeruginosa and P. agardhii decreased with decreasing cell quota of iron. The cell quota of phosphorus for M. aeruginosa decreased with decreasing cell quota of iron, whereas those for P. agardhii did not decrease. Iron uptake rate was measured in ironlimited batch cultures under different degrees of iron starvation. The results of the iron uptake experiments suggest that iron uptake rates are independent of the cell quota of iron for M. aeruginosa and highly dependent on the cell quota for P. agardhii. A kinetic model under iron limitation was developed based on the growth characteristics determined in our study, and this model predicted accurately the algal population growth and iron consumption. The model simulation suggested that M. aeruginosa is a superior competitor under iron limitation. The differences in growth characteristics between the species would be important determinants of the dominance of these algal species.