Overview Environmental toxicology refers to the scientific study of the potential effects upon organisms
of anthropogenic compounds released into the natural environment. A large variety of
chemicals, synthetic products and NCEs from unorganised sector are released in
environment every year. To this rather exhaustive list have been added the novel materials
like GMOs and Engineered Nano-Materials. The challenge is to create ways to efficiently
and credibly predict toxic potency and exposure levels for chemicals that lack toxicological
and exposure data in environmental settings. Both ethical and economic concerns over
animal testing demand the principles of replacement, reduction and refinement be pursued
for identification better tools to improve the efficiency of test design and field monitoring
targets particularly ecotoxicity testing. Hence, alternate animal models as well as alternate to
animal models are being explored more intensely today. Therefore, the development,
validation and application of high throughput terrestrial and aquatic invertebrate test
methods for ecotoxicity studies are high prioritity in ecotoxicology. The use, exposure and
effects information obtained from quantitative structure-activity relationships, read-across
methods, thresholds of toxicological concern and in vitro tests prior to in vivo testing are
ideal route for more rapid, efficient, and cost effective risk assessment of chemicals. The
application of "omics" approaches are expected to not only improve toxicity identification
and evaluation procedures for investigating complex chemical mixtures but also identify
when specific compounds are responsible for causing adverse effects. A major challenge is
development of diagnostic capabilities to determine cause-effect relationships within
impaired ecosystems. This will help in determining the extent to which existing remediation
strategies/technologies are effective, and the refinements needed in risk management.
Mission and Goals:
To explore cellular, genetic and organismal approaches for detection and mitigation of
environmental pollutants
Competencies:
Mechanism of toxicity of environmental pollutants
Sensors and probes for detection of biological contaminants
Remediation of soil, water and industrial wastes
Ecotoxicity and environmental impact assessment
Glimpses of Current Research Hazardous effect of tannery solid waste leachates on development and reproduction
in Drosophila melanogaster: 70 kDa heat shock protein as a marker of cellular
damage Rapid industrialization has increased the burden of chemicals in the environment. These
chemicals may be harmful to development and reproduction of any organism. We therefore
analyzed the adverse effects of leachates from a tannery solid waste on development and
reproduction using Drosophila. We show a significant delay in mean emergence of flies at
the higher concentrations of the leachates, indicating their effect on the organism's
development. Significant leachate-induction effect on reproduction of the organism was
observed by leachate induction. Sub-organismal analyses revealed Hsp70 expression and
tissue damage in a sex-specific manner. Refractoriness of Hsp70 expression in accessory
glands of male flies and ovaries of females was concurrent with tissue damage. Genes
encoding certain seminal proteins (Acp70A and Acp36DE) from accessory glands were
significantly down-regulated at higher concentrations of the leachates. The study suggests
that (i) sub-organismal adverse responses are reflected at organismal level, (ii) tannery
waste leachates cause adverse effects on the expression of genes encoding seminal
proteins that facilitate normal reproduction and (iii) Hsp70 may be used as a marker of
cellular damage for reproductive organs.
Siddique et.al. Ecotoxicology and Environmental Safety; 72: 1652-1662, 2009.
Effects of co-exposure of benzene, toluene and xylene to Drosophila melanogaster:
alteration in hsp70, hsp60, hsp83, hsp26, ROS generation and oxidative stress
markers Benzene, toluene and xylene are monocyclic aromatic hydrocarbon compounds, used both
as individual compound and as mixtures, in industry as well as household. Earlier studies
involving exposures to these compounds, individually, have shown that benzene was more
toxic compared to toluene or xylene. Here, we tested a working hypothesis that toluene
and/or xylene in a mixture containing benzene affect benzene induced toxicity in a nontarget
organism, Drosophila melanogaster. We exposed D. melanogaster larvae transgenic
for hsp70, hsp83 or hsp26 and wild type (Oregon R strain) larvae to 25.0-100.0mM benzene,
25.0-100.0mM toluene and 25.0-100mM xylene, individually or in mixtures. Subsequently,
we examined the expression of stress genes (encoding heat shock proteins, hsps),
generation of reactive oxygen species (ROS), induction of anti-oxidant stress markers and
emergence of flies under treatment as well as control conditions. We observed that all these
endpoints were significantly altered in all the treatment groups compared to their respective
controls. However, the magnitude of toxicity of a benzene-toluene (BT) or benzene-xylene
(BX) or benzene-toluene-xylene (BTX) mixture was significantly lower in the organism than
that of individual chemical. Our results also show the modulation of toluene toxicity by
xylene. Present study suggests antagonistic effect of xylene and toluene on benzene toxicity
and additive/synergistic effect of xylene on toluene induced toxicity. Thus, expression of
stress genes may be used as an assay for detection of early cellular toxicity. Further, our study supports the use of Drosophila as an alternative animal model for first tier screening of
adverse effects of chemical mixtures.
Singh et.al., Chemosphere; 79: 577-587,2010.