2019
DOI: 10.1016/j.envint.2019.105052
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Interspecies interactions between Microcystis aeruginosa PCC 7806 and Desmodesmus subspicatus SAG 86.81 in a co-cultivation system at various growth phases

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Cited by 15 publications
(10 citation statements)
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“…When the diatom Thalassiosira pseudonana was co-cultivated with the bacteria Dinoroseobacter shibae at a 1:1 ratio, the metabolism of T. pseudonana was altered, but its overall growth rate was unchanged (Paul et al, 2013). When cyanobacteria Microcystis aeruginosa PCC 7806 and microalga Desmodesmus subspicatus were cocultivated in a designated dialysis tubing, the presence of M. aeruginosa did not influence the growth of the microalga at the early logarithmic growth phase, while the microalga started to out-compete the co-cultivated bacteria during the exponential phase of growth (Omidi et al, 2019). These findings indicate that species, cultivation conditions and co-cultivation ratio can all influence the results of co-cultivation.…”
Section: Growth (Cell Number Chlorophyll Dry Weight) and Paramylon mentioning
confidence: 98%
“…When the diatom Thalassiosira pseudonana was co-cultivated with the bacteria Dinoroseobacter shibae at a 1:1 ratio, the metabolism of T. pseudonana was altered, but its overall growth rate was unchanged (Paul et al, 2013). When cyanobacteria Microcystis aeruginosa PCC 7806 and microalga Desmodesmus subspicatus were cocultivated in a designated dialysis tubing, the presence of M. aeruginosa did not influence the growth of the microalga at the early logarithmic growth phase, while the microalga started to out-compete the co-cultivated bacteria during the exponential phase of growth (Omidi et al, 2019). These findings indicate that species, cultivation conditions and co-cultivation ratio can all influence the results of co-cultivation.…”
Section: Growth (Cell Number Chlorophyll Dry Weight) and Paramylon mentioning
confidence: 98%
“…The Microcystis cultures were exposed for 7 days to daphnid extracts as opposed to spent Daphnia medium which is often employed to explore the effects of zooplankton on microalgae. The limitation of spent grazer medium is that its chemical composition is difficult to standardize so as to be fully equivalent to cyanobacterial medium (utilized for control samples) and it can also contain allelopathic metabolites released by the microalgae with which cladocerans were fed (Harel et al, 2013;Omidi et al, 2019). The extract concentrations corresponded to a daphnid abundance of 5, 25, 50, and 100 individuals (ind)/L, which is within the range observed in eutrophic lakes (Saunders et al, 1999;Hülsmann and Voigt, 2002;Wojtal-Frankiewicz et al, 2015).…”
Section: Introductionmentioning
confidence: 66%
“…Firstly, the Microcystis cultures were exposed to homogenized extracts of cladocerans to avoid the exposure to chemical compounds that are unrelated directly to daphnid presence and which may alter the study results. For example, spent Daphnia medium, even though its nutrient levels can be standardized, may contain metabolites originating from microalgae used to feed daphnids which in turn can cause severe cell lysis in Microcystis (Harel et al, 2013;Omidi et al, 2019;Qiu et al, 2019). One should, however, note that in situ only a fraction of daphnid molecules is released and could operate as infochemicals for cyanobacteria by triggering the defense mechanisms.…”
Section: Discussionmentioning
confidence: 99%
“…From the current literature, pure toxins, toxin containing crude extracts, filtrates of single and mixed cultures as well as the intact cells of the toxin producers induced different physiological and metabolic responses [ 25 , 94 , 219 ]. Another essential consideration for intraspecies interaction studies is the contribution of other secondary metabolites in addition to cyanotoxins.…”
Section: Discussionmentioning
confidence: 99%
“…It is important to repeat such experiments using log phase grown cells since there are many indications that those respond differently to biotic and abiotic conditions [ 93 ]. The stationary phase growth of D. subspicatus was also inhibited in co-cultivation with the MC-producing M. aeruginosa PCC 7806 and when exposed to the spent medium of Microcystis [ 94 ]. Filtrates from toxic M. aeruginosa induced colony formation in C. vulgaris , subject to the initial density of the green alga and the growth phase of M. aeruginosa , and with continuous field exposure inhibited the growth of the green alga [ 95 ].…”
Section: Cyanotoxins and Interspecies Interplaymentioning
confidence: 99%