Distinguishing the effects of Ce nanoparticles from their dissolution products : identification of transcriptomic biomarkers that are specific for ionic Ce in Chlamydomonas reinhardtii

Cerium (Ce) is a rare earth element that is incorporated in numerous consumer products, either in its cationic form or as engineered nanoparticles (ENPs). Given the propensity of small oxide particles to dissolve, it is unclear whether biological responses induced by ENPs will be due to the nanoparticles themselves or rather due to their dissolution. This study provides the foundation for the development of transcriptomic biomarkers that are specific for ionic Ce in the freshwater alga, Chlamydomonas reinhardtii, exposed either to ionic Ce or to two different types of small Ce ENPs (uncoated, ∼10 nm, or citrate-coated, ∼4 nm). Quantitative reverse transcription PCR was used to analyse mRNA levels of four ionic Ce-specific genes (Cre17g.737300, MMP6, GTR12, and HSP22E) that were previously identified by whole transcriptome analysis in addition to two oxidative stress biomarkers (APX1 and GPX5). Expression was characterized for exposures to 0.03–3 µM Ce, for 60–360 min and for pH 5.0–8.0. Near-linear concentration–response curves were obtained for the ionic Ce and as a function of exposure time. Some variability in the transcriptomic response was observed as a function of pH, which was attributed to the formation of metastable Ce species in solution. Oxidative stress biomarkers analysed at transcriptomic and cellular levels confirmed that different effects were induced for dissolved Ce in comparison to Ce ENPs. The measured expression levels confirmed that changes in Ce speciation and the dissolution of Ce ENPs greatly influence Ce bioavailability

A Multimethod Approach for Investigating Algal Toxicity of Platinum Nanoparticles

The ecotoxicity of platinum nanoparticles (PtNPs) widely used in for example automotive catalytic converters, is largely unknown. This study employs various characterization techniques and toxicity end points to investigate PtNP toxicity toward the green microalgae Pseudokirchneriella subcapitata and Chlamydomonas reinhardtii. Growth rate inhibition occurred in standard ISO tests (EC50 values of 15–200 mg Pt/L), but also in a double-vial setup, separating cells from PtNPs, thus demonstrating shading as an important artifact for PtNP toxicity. Negligible membrane damage, but substantial oxidative stress was detected at 0.1–80 mg Pt/L in both algal species using flow cytometry. PtNPs caused growth rate inhibition and oxidative stress in P. subcapitata, beyond what was accounted for by dissolved Pt, indicating NP-specific toxicity of PtNPs. Overall, P. subcapitata was found to be more sensitive toward PtNPs and higher body burdens were measured in this species, possibly due to a favored binding of Pt to the polysaccharide-rich cell wall of this algal species. This study highlights the importance of using multimethod approaches in nanoecotoxicological studies to elucidate toxicity mechanisms, influence of NP-interactions with media/organisms, and ultimately to identify artifacts and appropriate end points for NP-ecotoxicity testing

Combined Effects of Trace Metals and Light on Photosynthetic Microorganisms in Aquatic Environment

In the present review, we critically examine the state-of-the-art of the research on combined effects of trace metals and light on photosynthetic microorganisms in aquatic environment. Light of different intensity and spectral composition affects the interactions between trace metals and photosynthetic microorganisms directly, by affecting vital cellular functions and metal toxicokinetics and toxicodynamics, and indirectly, by changing ambient medium characteristics. Light radiation and in particular, the ultraviolet radiation component (UVR) alters the structure and reactivity of dissolved organic matter in natural water, which in most of the cases decreases its metal binding capacity and enhances metal bioavailability. The increase of cellular metal concentrations is generally associated with increasing light intensity, however further studies are necessary to better understand the underlying mechanisms. Studies on the combined exposures of photosynthetic microorganisms to metals and UVR reveal antagonistic, additive or synergistic interactions depending on light intensity, spectral composition or light pre-exposure history. Among the light spectrum components, most of the research was performed with UVR, while the knowledge on the role of high-intensity visible light and environmentally relevant solar light radiation is still limited. The extent of combined effects also depends on the exposure sequence and duration, as well as the species-specific sensitivity of the tested microorganisms and the activation of stress defense responses

Preface: Special Issue on Environmental Toxicology of Trace Metals

Trace metals (TMs) have a central role in the functioning of aquatic and terrestrial ecosystems. [...

Physicochemical aspects of lead bioaccumulation by Chlorella vulgaris

The relationship between lead speciation and its bioaccumulation by the alga Chlorella vulgaris was studied in the absence and presence of nitrilotriacetic, iminodiacetic, malonic, and citric acids. Pb uptake fluxes were rigorously analyzed by considering the simultaneous effects of metal transport in the medium coupled with metal complex dissociation kinetics. Under the conditions examined here, lead biouptake by C. vulgaris was governed by the free lead ion activity. Potentially labile hydrophilic complexes such as lead citrate and lead malonate did not contribute to the internalization fluxes. Kinetic modeling of the mass transport, adsorption reactions, and internalization fluxes confirmed the rate limiting role of the internalization flux. Comparison of the internalization and diffusive fluxes revealed that even in the presence of a large excess of Pb complexes, the supply of free ion (Pb2+) was sufficient to account for the observed Pb uptake. Pb adsorption to the cell surface was described by Langmuir isotherm. A new method was proposed as a means to estimate the number of Pb occupied transport sites at steady state. The apparent stability constant for the interaction of Pb with transport sites was determined to be 10(5.5) M(-1) at pH 6. Low temperature decreased both the Pb uptake flux and the Pb adsorbed to the transport sites. Pb uptake in the presence of Ca was competitively inhibited, and the binding affinity constant for Ca and transport sites was estimated to be 10(4.67) M(-1) at pH 6. Results were discussed within the perspective of the free ion activity and biotic ligand models. [on SciFinder (R)

Effect of pH on Pb biouptake by the freshwater alga Chlorella kesslerii

The effect of pH on Pb bioaccumulation by Chlorella kesslerii was studied. Both Pb uptake fluxes and Pb bound to membrane transport sites increased with an increase in pH from 4.0-5.0, were relatively stable in the pH interval 5.0-6.5, and increased again at pH 7.0 and 8.0. Protons affected Pb adsorption to the algal surface by competing directly for surface sites, by modifying the overall algal surface charge and by modifying the chem. speciation of Pb in soln. These results indicate a failure of the free-ion activity or biotic ligand models above pH 6.5, possibly due to the bioaccumulation of hydroxo or carbonato Pb complexes. [on SciFinder (R)