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1.
Int J Mol Sci ; 18(3)2017 Mar 02.
Article in English | MEDLINE | ID: mdl-28257097

ABSTRACT

Accurately assessing the toxicity of complex, environmentally relevant mixtures remains an important challenge in ecotoxicology. The goal was to identify biological effects after exposure to environmental water samples and to determine whether the observed effects could be explained by the waterborne metal mixture found in the samples. Zebrafish embryos were exposed to water samples of five different sites originating from two Flemish (Mol and Olen, Belgium) metal contaminated streams: "Scheppelijke Nete" (SN) and "Kneutersloop" (K), and a ditch (D), which is the contamination source of SN. Trace metal concentrations, and Na, K, Mg and Ca concentrations were measured using ICP-MS and were used to reconstitute site-specific water samples. We assessed whether the effects that were observed after exposure to environmental samples could be explained by metal mixture toxicity under standardized laboratory conditions. Exposure to "D" or "reconstituted D" water caused 100% mortality. SN and reconstituted SN water caused similar effects on hatching, swim bladder inflation, growth and swimming activity. A canonical discriminant analysis confirmed a high similarity between both exposure scenarios, indicating that the observed toxicity was indeed primarily caused by metals. The applied workflow could be a valuable approach to evaluate mixture toxicity that limits time and costs while maintaining biological relevance.


Subject(s)
Complex Mixtures/toxicity , Embryo, Nonmammalian/drug effects , Water Pollutants, Chemical/analysis , Animals , Discriminant Analysis , Embryonic Development/drug effects , Heavy Metal Poisoning , Poisoning , Zebrafish
2.
Water Res ; 99: 129-139, 2016 08 01.
Article in English | MEDLINE | ID: mdl-27153115

ABSTRACT

Because of the ever increasing complexity of environmental contamination profiles, there are limitations to the use of analytical pollutant measurements for monitoring and prioritization of watercourses. The potential of biomarkers has been debated for many years, especially in laboratory settings, but there is a need for studies evaluating these approaches in the field. We evaluated the usefulness of a selection of biomarkers, mostly indicators of general physiological status and common stress responses such as oxidative stress, to discriminate among environmental pollution profiles, with the aim of prioritizing contaminated watercourses for targeted remediation efforts. To this end, juvenile common carp (Cyprinus carpio Lin.) were exposed in cages in the field to Flemish watercourses with varying pollution profiles. After six weeks of exposure, the bioaccumulation of key pollutants was measured, and a set of organismal, biochemical and transcriptional endpoints was determined in several tissue types. After data integration a discrete set of 14 parameters was identified, that could successfully distinguish all watercourses from each other. We show that an integrated biomarker approach, mainly targeting common stress responses, can offer the resolving power to discriminate among environmentally relevant exposure scenarios, and a means to prioritize watercourses for targeted remediation.


Subject(s)
Biomarkers/metabolism , Carps , Animals , Environmental Exposure , Oxidative Stress
3.
Altern Lab Anim ; 43(2): 89-100, 2015 May.
Article in English | MEDLINE | ID: mdl-25995012

ABSTRACT

Developmental toxicity testing could greatly benefit from the availability of an in vitro alternative model based on the use of animal embryos that have better human-like physiology than the currently-used alternative models. These current models are insufficient, as extrapolation of the results can be challenging. Therefore, an in vitro bovine embryo culture system was used to expose individual morulae to test substances, and to study developmental characteristics up to the blastocyst stage. Cadmium was chosen as the reference toxicant to investigate the sensitivity of the bovine morulae to various concentrations and exposure times. Oocytes from slaughterhouse-obtained bovine ovaries, were maturated, fertilised and cultured up until the morula stage. Morulae were exposed to different cadmium concentrations for 18 or 70 hours, and developmental competence, embryo quality and the expression of cadmium exposure-related genes were evaluated. Cadmium exposure hampered embryonic developmental competence and quality. Compared with the 18-hour exposure, the 70-hour exposure induced a 20-fold higher toxic response with regard to developmental competence and a more 'cadmium-typical' transcript expression. The bovine morula might be a promising tool for toxicity testing as, following exposure, the embryos reacted in a sensitive and 'cadmium-typical' manner to our reference toxicant.


Subject(s)
Cadmium/toxicity , Animals , Blastocyst/drug effects , Cattle , In Vitro Techniques , Morula/drug effects , Oxidative Stress , RNA, Messenger/analysis
4.
PLoS One ; 10(4): e0123285, 2015.
Article in English | MEDLINE | ID: mdl-25855985

ABSTRACT

Thyroid hormone (TH) balance is essential for vertebrate development. Deiodinase type 1 (D1) and type 2 (D2) increase and deiodinase type 3 (D3) decreases local intracellular levels of T3, the most important active TH. The role of deiodinase-mediated TH effects in early vertebrate development is only partially understood. Therefore, we investigated the role of deiodinases during early development of zebrafish until 96 hours post fertilization at the level of the transcriptome (microarray), biochemistry, morphology and physiology using morpholino (MO) knockdown. Knockdown of D1+D2 (D1D2MO) and knockdown of D3 (D3MO) both resulted in transcriptional regulation of energy metabolism and (muscle) development in abdomen and tail, together with reduced growth, impaired swim bladder inflation, reduced protein content and reduced motility. The reduced growth and impaired swim bladder inflation in D1D2MO could be due to lower levels of T3 which is known to drive growth and development. The pronounced upregulation of a large number of transcripts coding for key proteins in ATP-producing pathways in D1D2MO could reflect a compensatory response to a decreased metabolic rate, also typically linked to hypothyroidism. Compared to D1D2MO, the effects were more pronounced or more frequent in D3MO, in which hyperthyroidism is expected. More specifically, increased heart rate, delayed hatching and increased carbohydrate content were observed only in D3MO. An increase of the metabolic rate, a decrease of the metabolic efficiency and a stimulation of gluconeogenesis using amino acids as substrates may have been involved in the observed reduced protein content, growth and motility in D3MO larvae. Furthermore, expression of transcripts involved in purine metabolism coupled to vision was decreased in both knockdown conditions, suggesting that both may impair vision. This study provides new insights, not only into the role of deiodinases, but also into the importance of a correct TH balance during vertebrate embryonic development.


Subject(s)
Embryonic Development/genetics , Iodide Peroxidase/genetics , Zebrafish/genetics , Adenosine Triphosphate/metabolism , Animals , Embryo, Nonmammalian , Energy Metabolism/genetics , Gene Expression Regulation, Developmental , Iodide Peroxidase/metabolism , Light Signal Transduction , Muscle Development/genetics , Thyroid Hormones/genetics , Thyroid Hormones/metabolism , Zebrafish/growth & development , Iodothyronine Deiodinase Type II
5.
Environ Sci Pollut Res Int ; 21(20): 11856-66, 2014 Oct.
Article in English | MEDLINE | ID: mdl-24385186

ABSTRACT

Bioaccumulation of perfluorooctane sulfonate (PFOS) in a restricted terrestrial food chain was investigated with the omnivorous wood mouse (Apodemus sylvaticus) on top of the studied food chain. The levels detected are very high compared with literature as a result of the presence of fluorochemical plant in the immediate vicinity of the study area. Soil, surface water, fruits of European elder and common blackberry, invertebrates, bank vole and wood mouse were collected at two sites, e.g. Blokkersdijk, adjacent to the fluorochemical plant, and Galgenweel, a reference site 2 km further away. In wood mouse, the highest PFOS concentrations were found in the liver followed by the pancreas, lungs and kidneys, with the spleen having the lowest levels. In the liver, the concentrations ranged from 787 to 22,355 ng/g ww at Blokkersdijk and these were significantly correlated with those detected in the kidneys (13.7-4,226 ng/g ww). If current results are compared to the findings of a previous study conducted in 2002 at the same sites, a significant decrease of PFOS in livers of wood mouse is observed. To the best of our knowledge, so far no studies reported levels of PFOS in terrestrial invertebrates under field conditions. At Blokkersdijk, PFOS was detected in all invertebrate species ranging from 28 to 9,000 ng/g. Soil and water were also contaminated with levels of respectively 68 ng/g and 22 ng/L. Biota-to-soil accumulation factors ranged from 0.11 to 68 for earthworms. Biomagnification factors (BMFs) of liver wood mouse/berries were as high as 302. BMFs for invertebrates were remarkably lower (up to 2).


Subject(s)
Alkanesulfonic Acids/analysis , Ecosystem , Environmental Monitoring/methods , Environmental Pollutants/analysis , Fluorocarbons/analysis , Hydrocarbons, Fluorinated/chemistry , Animals , Belgium , Female , Food Chain , Fruit/chemistry , Geography , Invertebrates/metabolism , Liver/metabolism , Male , Mice , Soil/chemistry , Time Factors , Water/chemistry
6.
Chemosphere ; 91(4): 521-9, 2013 Apr.
Article in English | MEDLINE | ID: mdl-23332880

ABSTRACT

Despite the fact that aquatic organisms are mostly poikilothermic and environmental temperature variations can have considerable impact on chemical toxicity, toxicity studies are mainly performed at the species' specific standard or optimal temperature. Since the zebrafish is a recommended test species for use in toxicity tests, we investigated the temperature dependence of 96 h cadmium accumulation and toxicity in zebrafish acclimated to 18, 26, 30 or 34°C. Zebrafish showed high cadmium tolerance with acute 96 h LC50 values of 121.5, 102.4, 124.6 and 126.7 µM at 18, 26, 30 and 34°C respectively. Differences in cadmium toxicity at the different temperatures were small and toxicity did not increase with increasing temperature as is often suggested. We did however observe an interesting concentration dependent crossover pattern in which the temperature dependence at the highest exposure concentrations was exactly opposite to the pattern at the lower concentrations. At the highest concentrations the following order of toxicity was observed: 26°C>18°C>30°C>34°C. Possibly, either the warm acclimation provoked a general stress response which protected organisms against future severe stress situations, or resulted in specific defence mechanisms which also provided protection against cadmium exposure. Although at 18°C cadmium accumulation decreased more than would be expected based on the metabolic rate, cadmium toxicity was not proportionately decreased. This increased cadmium sensitivity in the cold was likely due to the combined effect of low temperature and cadmium exposure on sodium loss. This study shows that the temperature dependence of cadmium toxicity results from the combination of altered cadmium accumulation and sensitivity. Inclusion of the temperature effect in the calculation of environmental quality standards may have to be considered to ensure that more sensitive species are also protected at suboptimal temperatures.


Subject(s)
Cadmium/metabolism , Temperature , Water Pollutants, Chemical/metabolism , Zebrafish/physiology , Acclimatization , Animals , Cadmium/toxicity , Water Pollutants, Chemical/toxicity
7.
J Comp Physiol B ; 183(1): 109-21, 2013 Jan.
Article in English | MEDLINE | ID: mdl-22872185

ABSTRACT

The zebrafish has become a valuable vertebrate model organism in a wide range of scientific disciplines, but current information concerning the physiological temperature response of adult zebrafish is rather scarce. In this study, zebrafish were experimentally acclimated for 28 days to 18, 26 or 34 °C and a suite of non-invasive and invasive methods was applied to determine the thermal dependence of zebrafish physiological condition. With decreasing temperature, the metabolic rate of zebrafish decreased, as shown by the decreasing oxygen uptake and ammonia excretion rates, limiting the critical swimming speed, probably due to a decreased muscle fibre power output. In response to exercise, fuel stores were mobilized to the liver as shown by the increased hepatosomatic index, liver total absolute energetic value and liver carbohydrate concentration but due to the low metabolic rate they could not be adequately addressed to power swimming activity at 18 °C. Conversely, the increased metabolic performance at high temperature came with an increased metabolic cost resulting in decreased energy status reflected particularly well by the non-invasive condition factor and invasive measures of carcass protein concentration, carcass total absolute energetic value and liver carbohydrate concentration. We showed that the combined measurement of the relative condition factor and critical swimming speed is a powerful non-invasive tool for long-term follow-up studies. Invasive methods were redundant for measuring general energy status but they provided detailed information concerning metabolic reorganization. With this study we proved that the usefulness of the zebrafish as a model organism can easily be expanded to include physiological studies and we provided a reference dataset for the selection of measures of physiological responses for future studies using the zebrafish.


Subject(s)
Acclimatization , Energy Metabolism , Models, Biological , Physical Conditioning, Animal , Zebrafish/physiology , Ammonia/metabolism , Animals , Behavior, Animal , Body Size , Carbohydrate Metabolism , Female , Fish Proteins/analysis , Fish Proteins/biosynthesis , Hot Temperature/adverse effects , Liver/growth & development , Liver/metabolism , Oxygen Consumption , Swimming , Zebrafish/growth & development
8.
Aquat Toxicol ; 126: 52-62, 2013 Jan 15.
Article in English | MEDLINE | ID: mdl-23143039

ABSTRACT

Standard ecotoxicity tests are performed at species' specific standard temperatures, but temperature is known to affect chemical toxicity. A temperature increase has been shown to increase cadmium toxicity in several aquatic species but information in fish is scarce. Based on literature we hypothesize that with increasing temperature, cadmium accumulation and oxidative stress increase, resulting in increased toxicity. In this study zebrafish acclimated to 12, 18, 26 (standard temperature) or 34°C for one month, were exposed to 5 µM cadmium for 4 or 28 days at the respective acclimation temperature. Cadmium toxicity (mortality) increased with increasing temperature. PCA showed that the high mortality at 34°C was closely correlated to an increasing tissue cadmium accumulation with increasing temperature, but not to liver oxidative damage under the form of protein carbonyl content or lipid peroxidation (measured as malondialdehyde levels) or liver antioxidative potential. Instead, acclimation to 12°C induced the highest oxidative damage to liver proteins and lipids, and transcript levels of glucose-6P-dehydrogenase, 6P-gluconate-dehydrogenase and glutathione peroxidase were particularly good markers of cold-induced oxidative stress. At this low temperature there was no interaction with cadmium exposure and there was no sign of cadmium sensitivity. Contrastingly, the combined effect of high temperature and cadmium exposure on mortality proved synergistic. Therefore we conclude that interactions between temperature and cadmium toxicity increased with increasing temperature and that this probably played part in increasing cadmium sensitivity. Increased cadmium compartmentalization and protein carbonyl content in liver of zebrafish acclimated to the standard temperature of 26°C probably played part in increased sensitivity towards the same cadmium body burden compared to lower temperatures. On the one hand we recognize and this study even confirms the importance of applying standard temperatures in standard ecotoxicity tests to ensure inter-study comparability. On the other hand temperatures in the field may deviate from standard temperatures and accounting for deviating temperatures, which can alter chemical sensitivity, in regulation can improve environmental protection.


Subject(s)
Cadmium/toxicity , Liver/pathology , Temperature , Water Pollutants, Chemical/toxicity , Zebrafish/physiology , Animals , Cadmium/analysis , Cadmium/metabolism , Gene Expression Profiling , Liver/chemistry , Liver/drug effects , Oxidative Stress/drug effects , Principal Component Analysis , Survival Analysis , Tissue Distribution , Water/chemistry , Water Pollutants, Chemical/analysis
9.
Chemosphere ; 89(7): 869-75, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22658941

ABSTRACT

For several decades, perfluorooctane sulfonate (PFOS) has widely been used as a fluorinated surfactant in aqueous film forming foams used as hydrocarbon fuel fire extinguishers. Due to concerns regarding its environmental persistence and toxicological effects, PFOS has recently been replaced by novel fluorinated surfactants such as Forafac®1157, developed by the DuPont company. The major component of Forafac®1157 is a 6:2 fluorotelomer sulfonamide alkylbetaine (6:2 FTAB), and a link between the trade name and the exact chemical structure is presented here to the scientific community for the first time. In the present work, the structure of the 6:2 FTAB was elucidated by (1)H, (13)C and (19)F nuclear magnetic resonance spectroscopy and high-resolution mass spectrometry. Moreover, its major metabolites from blue mussel (Mytilus edulis) and turbot (Scophthalmus maximus) and its photolytic transformation products were identified. Contrary to what has earlier been observed for PFOS, the 6:2 FTAB was extensively metabolized by blue mussel and turbot exposed to Forafac®1157. The major metabolite was a deacetylated betaine species, from which mono- and di-demethylated metabolites also were formed. Another abundant metabolite was the 6:2 fluorotelomer sulfonamide. In another experiment, Forafac®1157 was subjected to UV-light induced photolysis. The experimental conditions aimed to simulate Arctic conditions and the deacetylated species was again the primary transformation product of 6:2 FTAB. A 6:2 fluorotelomer sulfonamide was also formed along with a non-identified transformation product. The environmental presence of most of the metabolites and transformation products was qualitatively demonstrated by analysis of soil samples taken in close proximity to an airport fire training facility.


Subject(s)
Soil Pollutants/metabolism , Surface-Active Agents/metabolism , Alkanesulfonic Acids/analysis , Alkanesulfonic Acids/metabolism , Animals , Flatfishes/metabolism , Fluorocarbons/analysis , Fluorocarbons/metabolism , Magnetic Resonance Spectroscopy , Mass Spectrometry , Mytilus edulis/metabolism , Photolysis , Soil Pollutants/analysis , Surface-Active Agents/analysis , Ultraviolet Rays
10.
Ecotoxicology ; 20(2): 447-56, 2011 Mar.
Article in English | MEDLINE | ID: mdl-21253836

ABSTRACT

Perfluorinated organic chemicals like perfluorooctane sulfonic acid (PFOS) are persistent environmental pollutants that have been measured in a great diversity of wildlife worldwide, especially in the aquatic compartment. However, little information is available on the presence and effects of PFOS in the terrestrial compartment. Therefore, we investigated in this project the risks for effects, bioaccumulation and potential mechanisms of activity of PFOS in the bumblebee Bombus terrestris L. (Hymenoptera: Apidae) that is an important worldwide pollinator in the terrestrial compartment of wildflowers and cultivated crops. The exposure to PFOS occurred orally via the drinking of treated sugar water in a wide range from 1 µg/l up to 10 mg/l, containing environmentally relevant as well as high concentrations, and this was done with use of microcolonies of B. terrestris in the laboratory. A chronic toxicity assay demonstrated high bumblebee worker mortality (up to 100%) with an LC(50) of 1.01 mg/l (R(2) = 0.98). In addition, PFOS posed strong detrimental reproductive effects, and these concerted with a dramatic reduction in ovarian size. HPLC-MS demonstrated a bioaccumulation factor of 27.9 for PFOS in bumblebee workers fed with sugar water containing 100 µg/l PFOS during 5 weeks (2184 ± 365 ng/g BW). Finally, potential mechanisms of activity were investigated to explain the significant impact of PFOS on survival and reproduction capacity of B. terrestris. Exposure of bumblebee workers to PFOS resulted in a significant decrease in mitochondrial electron transport activity (p = 0.035) and lipid amounts (p = 0.019), while the respective p-values were 0.58 and 0.12 for protein and glucose amounts. Hence, addition of PFOS to ecdysteroid responsive Drosophila melanogaster S2 cells resulted in a strong antagonistic action on the EcR-b.act.luc reporter construct, demonstrating that PFOS may exert its effects partially through an endocrine disrupting action via the insect molting hormone or ecdysteroid receptor.


Subject(s)
Alkanesulfonic Acids/toxicity , Bees/drug effects , Environmental Pollutants/toxicity , Fluorocarbons/toxicity , Animals , Bees/metabolism , Electron Transport/drug effects , Feeding Behavior/drug effects , Pollination/drug effects , Reproduction/drug effects
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