BIOECOTOX · Biomarkers: the early warning sentinel of chemical pollution risk assessment
FP6 — Marie Curie Actions (Human Resources and Mobility)
- Duration
- 2004-09-01 → 2006-08-31
- EU contribution
- €151,287
- Participants
- 1
- Scheme
- EIF
Lines connect the coordinator with its partners. CORDIS does not always give exact coordinates for projects before 2014. These points are placed at city or country level.
Results in brief
Final Activity Report Summary - BIOECOTOX (Biomarkers: the early warning sentinel of chemical pollution risk assessment)
Water quality is impacted by several anthropogenic pressures, which impair the value of aquatic ecosystem and sustainable use of water resources. The EU policy (e.g. Water Framework Directive) requires development of bioindicators in order to monitor and assess water quality and aquatic ecosystem health. Biomarkers have long been recognised as useful tools for the environmental risk assessment in aquatic ecosystems. We define biomarkers as rapid, measurable changes occurring at lower levels of biological organisation (biochemical, molecular and cellular) as a consequence of exposure to pollutants. Ecotoxicogenomic, defined as the study of gene and protein expression in responses to environmental toxicant exposures, is an emerging field which intended to develop new molecular biomarkers to assess ecotoxicological stress at an early stage and to explain its mode of action. Moreover, some biomarker responses might be transient and adaptive, whereas other might be followed by later changes at tissue or organism level which ultimately affect populations and whole ecosystems. In this scenario, the BIOECOTOX project proposed to use a recent and very sensitive technique, the Real Time PCR (RT-PCR) to assess the effects of pollutants at the expression level of genes of the model organism Saccaromyces cerevisiae which is a very common yeast (e.g. ingredient in beer and bread). Two aquatic pollutants of concern, belonging to two different chemical families, Benzo(a)pyrene (B(a)P) and Cadmium (Cd) were tested focusing on two crucial points(1) non toxic concentrations assessed by whole-organism responses in standardised methods (No Observed Effect Concentration or NOEC and Predicted No Effect Concentration or PNEC) and (2) full life cycle of the organism to predict the influence of life cycle on genes responses. Considering our objective to develop those molecular biomarkers for EU legislation a particular attention was brought to the quality control and the validation of our results. None of the six tested genes were modified by the B(a)P but their responses varied with life cycle. Because we didn't observed any toxicity on the cell growth even at highest concentrations, we hypothesised that S. cerevisiae may not to be the relevant organism to detect B(a)P contamination. On the other hand, among the ten selected genes to detect cadmium, nine of them were induced after 4h exposure. Such results showed that the RT-PCR approach allowed us to investigate genes profiles in yeast at different life stage (B(a)P and Cd) and discriminate this natural variation from the deleterious effect of pollutants (Cd). This technique also allowed detecting very low concentrations of cadmium which are not detected by traditional toxicological methods based on whole-organism responses and confirmed mechanisms of action for cadmium detoxification at environmental level. Finally, the results of the BIOECOTOX project identified nine genes as promising early warning indicators of exposure to and effects of cadmium on the eukaryotic organisms in the environment.
Data: CORDIS, © European Union
Project objective
Nowadays the risk assessment of chemical pollutions is considered essential to be evaluated on measurement of the biological effects and not only on chemical analysis of environmental samples because this approach does not provide any indication of deleterious effects on living organisms. To this demand, recently the biological markers, or biomarkers which can be defined as indicator of normal physiology alteration, emerged as extremely important to monitor the pollutant impact as well as to assess the toxic effects on the environmental health. Further, new technologies mainly based on post genomic era, which combine the studies of the gene expression at level of mRNA and protein highlighted more and more questions related to the concept of the risk assessment as well as the definition of safety margin of a chemical in the environment. In this scenario, our project proposes a new method based mainly on a very sensitive technique to monitor the effects of pollutants at transcription level (mRNA) of known biomarkers. For this purpose, two biological models will be exposed to different concentrations of marine pollutants (i.e. heavy metals and organic compound) and the known biomarkers (i.e. Metallothionein, Cytochrome P450) will be analysed at level of mRNA transcription using the Real Time Quantitative PCR (Q-PCR), which allows to detect very small changes at level of mRNA expression. Our attention will be focused on two crucial concentrations of pollutants, the one that so far is considered according to the European policies; the dose without any toxic effect and it is probably that our method could already detect an effect at molecular level. The other concentration will be used to study the so called chronic effect" of a compound. A very low dose effect will be analysed in a long-term exposure and also in this case the " sentinel" will be the biomarker mRNA expression. The researcher would like to continue this work in her home country."
Original text from CORDIS.
Participants
- EUROPEAN COMMISSION - GENERAL DIRECTORATE - JOINT RESEARCH CENTER · ISPRA (VA)CoordinatorCountry levelItaly
Links
Data: CORDIS, © European Union
