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We explored the potential of chemosynthetic microorganisms growing at high temperatures to induce the release of key elements (mainly iron, silicon, and magnesium) involved in the known toxic properties (iron content and fibrous mineral shapes) of asbestos minerals. We show for the first time that the microbial respiration of iron from amphibole asbestos releases some of the iron contained in the mineral while supporting microbial growth.

Amphibole asbestos is related to lung fibrosis and several types of lung tumors. The disease-triggering mechanisms still challenge our diagnostic capabilities and are still far from being fully understood. The literature focuses primarily on the role and formation of asbestos bodies in lung tissues, but there is a distinct lack of studies on amphibole particles that have been internalized by alveolar epithelial cells (AECs). These internalized particles may directly interact with the cell nucleus and the organelles, exerting a synergistic action with asbestos bodies (AB) from a different location. Here we document the near-atomic- to nano-scale transformations induced by, and taking place within, AECs of three distinct amphiboles (anthophyllite, grunerite, “amosite”) with different Fe-content and morphologic features. We show that: (i) an Fe-rich layer is formed on the internalized particles, (ii) particle grain boundaries are transformed abiotically by the internal chemical environment of AECs and/or by a biologically induced mineralization mechanism, (iii) the Fe-rich material produced on the particle surface does not contain large amounts of P, in stark contrast to extracellular ABs, and (iv) the iron in the Fe-rich layer is derived from the particle itself. Internalized particles and ABs follow two distinct formation mechanisms reaching different physicochemical end-states.

Fine particulate matter (PM2.5) can adversely affect human health. Emissions from residential energy sources have the largest impact on premature mortality globally, but their pathological and molecular implications on cellular physiology are still elusive. In the present study potential molecular consequences were investigated during long-term exposure of human bronchial epithelial BEAS-2B cells to PM2.5, collected from a biomass power plant. Initially, we observed that PM2.5 did not affect cellular survival or proliferation. However, it triggered an activation of the stress response p38 MAPK which, along with RhoA GTPase and HSP27, mediated morphological changes in BEAS-2B cells, including actin cytoskeletal rearrangements and paracellular gap formation. The p38 inhibitor SB203580 prevented phosphorylation of HSP27 and ameliorated morphological changes. During an intermediate phase of long-term exposure, PM2.5 triggered proliferative regression and activation of an adaptive stress response necessary to maintain energy homeostasis, including AMPK, repression of translational elongation, and autophagy. Finally, accumulation of intracellular PM2.5 promoted lysosomal destabilization and cell death, which was dependent on lysosomal hydrolases and p38 MAPK, but not on the inflammasome and pyroptosis. TEM images revealed formation of protrusions and cellular internalization of PM2.5, induction of autophagosomes, amphisomes, autophagosome-lysosomal fusion, multiple compartmental fusion, lysosomal burst, swollen mitochondria and finally necrosis. In consequence, persistent exposure to PM2.5 may impair epithelial barriers and reduce regenerative capacity. Hence, our results contribute to a better understanding of PM-associated lung and systemic diseases on the basis of molecular events.

International audience; New efficient approaches to the characterization of fly ash and particulate matter (PM) have to be developed in order to better understand their impacts on environment and health. Polycyclic aromatic hydrocarbons (PAH) contained in PM from biomass burning have been identified as genotoxic and cytotoxic, and some tools already exist to quantify their contribution to PM. Optical fluorescence microscopy is proposed as a rapid and relatively economical method to allow the quantification of PAH in different particles emitted from biomass combustion. In this study samples were collected in the flue gas of biomass-combustion facilities with nominal output ranging from 40 kW to 17.3 MW. The fly ash samples were collected with various flue gas treatment devices (multicyclone, baghouse filter, electrostatic precipitator); PM samples were fractionated from the flue gas with a DEKATI® DGI impactor. A method using fluorescence observations (at 470 nm), white-light observations and image processing has been developed with the aim of quantifying fluorescence per sample. Organic components of PM and fly ash, such as PAH, humic-like substances (HULIS) and water-soluble organic carbon (WSOC) were also quantified. Fluorescence microscopy analysis method assessment was first realized with fly ash that was artificially coated with PAH and HULIS. Total amounts of PAH in the three size fractions of actual PM from biomass burning strongly correlated with the intensities of fluorescence. These encouraging results contribute to the development of a faster and cheaper method of quantifying particle-bound PAH.

PURPOSE:This study was designed to assess the fate and the overall potential impacts of the widely prescribed drugs ranitidine and tramadol after their introduction into the aquatic environment.METHODS:The probability to detect these two drugs in the aquatic environment was studied by analyzing their abiotic and biotic degradation properties. For this purpose, samples were irradiated with different light sources, and three widely used biodegradability tests from the OECD series, the closed bottle test (OECD 301 D), the manometric respirometry test (OECD 301 F) and the Zahn-Wellens test (OECD 302 B), were conducted. The ecotoxicity of the photolytically formed transformation products was assessed by performing the bacterial growth inhibition test (EN ISO 10712). Furthermore, quantitative structure-activity relationship analysis and a risk analysis based on the calculation of the predicted environmental concentrations have also been conducted to assess the environmental risk potential of the transformation products. The possible formation of stable products by microbial or photolytical transformation has been investigated with DOC and LC-MS analytics.RESULTS:In the present study, neither ranitidine, nor tramadol, nor their photoderivatives were found to be readily or inherently biodegradable according to test guidelines. The photolytic transformation was faster under a UV lamp compared to the reaction under an Xe lamp with a spectrum that mimics sunlight. No chronic toxicity against bacteria was found for ranitidine or its photolytic decomposition products, but a low toxicity was detected for the resulting mixture of the photolytic transformation products of tramadol.CONCLUSIONS:The study demonstrates that transformation products may have a higher environmental risk potential than the respective parent compounds. Purpose This study was designed to assess the fate and theoverall potential impacts of the widely prescribed drugsranitidine and tramadol after their introduction into theaquatic environment.Methods The probability to detect these two drugs in theaquatic environment was studied by analyzing their abioticand biotic degradation properties. For this purpose, sampleswere irradiated with different light sources, and threewidely used biodegradability tests from the OECD series,the closed bottle test (OECD 301 D), the manometricrespirometry test (OECD 301 F) and the Zahn–Wellens test(OECD 302 B), were conducted. The ecotoxicity of thephotolytically formed transformation products was assessedby performing the bacterial growth inhibition test (EN ISO10712). Furthermore, quantitative structure–activity relationshipanalysis and a risk analysis based on the calculation of thepredicted environmental concentrations have also been conductedto assess the environmental risk potential of thetransformation products. The possible formation of stableproducts by microbial or photolytical transformation has beeninvestigated with DOC and LC-MS analytics.Results In the present study, neither ranitidine, nor tramadol,nor their photoderivatives were found to be readily orinherently biodegradable according to test guidelines. Thephotolytic transformation was faster under a UV lampcompared to the reaction under an Xe lamp with a spectrumthat mimics sunlight. No chronic toxicity against bacteriawas found for ranitidine or its photolytic decompositionproducts, but a low toxicity was detected for the resultingmixture of the photolytic transformation products oftramadol.Conclusions The study demonstrates that transformationproducts may have a higher environmental risk potentialthan the respective parent compounds.

New efficient approaches to the characterization of fly ash and particulate matter (PM) have to be developed in order to better understand their impacts on environment and health. Polycyclic aromatic hydrocarbons (PAH) contained in PM from biomass burning have been identified as genotoxic and cytotoxic, and some tools already exist to quantify their contribution to PM. Optical fluorescence microscopy is proposed as a rapid and relatively economical method to allow the quantification of PAH in different particles emitted from biomass combustion. In this study samples were collected in the flue gas of biomass-combustion facilities with nominal output ranging from 40 kW to 17.3 MW. The fly ash samples were collected with various flue gas treatment devices (multicyclone, baghouse filter, electrostatic precipitator); PM samples were fractionated from the flue gas with a DEKATI® DGI impactor. A method using fluorescence observations (at 470 nm), white-light observations and image processing has been developed with the aim of quantifying fluorescence per sample. Organic components of PM and fly ash, such as PAH, humic-like substances (HULIS) and water-soluble organic carbon (WSOC) were also quantified. Fluorescence microscopy analysis method assessment was first realized with fly ash that was artificially coated with PAH and HULIS. Total amounts of PAH in the three size fractions of actual PM from biomass burning strongly correlated with the intensities of fluorescence. These encouraging results contribute to the development of a faster and cheaper method of quantifying particle-bound PAH.Copyright 2015 American Association for Aerosol Research

New efficient approaches to the characterization of fly ash and particulate matter (PM) have to be developed in order to better understand their impacts on environment and health. Polycyclic Aromatic Hydrocarbons (PAH) contained in PM from biomass burning have been identified as genotoxic and cytotoxic, and some tools already exist to quantify their contribution to PM. Optical fluorescence microscopy is proposed as a rapid and relatively economical method to allow the quantification of PAH in different particles emitted from biomass combustion. In this study samples were collected in the flue gas of biomass-combustion facilities with nominal output ranging from 40 kW to 17.3 MW. The fly ash samples were collected with various flue gas treatment devices (multicyclone, baghouse filter, electrostatic precipitator); PM samples were fractionated from the flue gas with a DEKATI® DGI impactor. A method using fluorescence observations (at 470 nm), white-light observations and image processing has been developed with the aim of quantifying fluorescence per sample. Organic components of PM and fly ash, such as PAH, Humic-Like Substances (HULIS) and water-soluble organic carbon (WSOC) were also quantified. Fluorescence microscopy analysis method assessment was firstly realized with fly ash that was artificially coated with PAH and HULIS. Total amounts of PAH in the three size fractions of actual PM from biomass burning strongly correlated with the intensities of fluorescence. These encouraging results contribute to the development of a faster and cheaper method of quantifying particle-bound PAH.

New efficient approaches to the characterization of fly ash and particulate matter (PM) have to be developed in order to better understand their impacts on environment and health. Polycyclic aromatic hydrocarbons (PAH) contained in PM from biomass burning have been identified as genotoxic and cytotoxic, and some tools already exist to quantify their contribution to PM. Optical fluorescence microscopy is proposed as a rapid and relatively economical method to allow the quantification of PAH in different particles emitted from biomass combustion. In this study samples were collected in the flue gas of biomass-combustion facilities with nominal output ranging from 40 kW to 17.3 MW. The fly ash samples were collected with various flue gas treatment devices (multicyclone, baghouse filter, electrostatic precipitator); PM samples were fractionated from the flue gas with a DEKATI® DGI impactor. A method using fluorescence observations (at 470 nm), white-light observations and image processing has been developed with the aim of quantifying fluorescence per sample. Organic components of PM and fly ash, such as PAH, humic-like substances (HULIS) and water-soluble organic carbon (WSOC) were also quantified. Fluorescence microscopy analysis method assessment was first realized with fly ash that was artificially coated with PAH and HULIS. Total amounts of PAH in the three size fractions of actual PM from biomass burning strongly correlated with the intensities of fluorescence. These encouraging results contribute to the development of a faster and cheaper method of quantifying particle-bound PAH.Copyright 2015 American Association for Aerosol Research