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<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:contributor>Richard S. Halbrook</dc:contributor>
  <dc:contributor>John B. French</dc:contributor>
  <dc:creator>Dawn M. Fallacara</dc:creator>
  <dc:date>2011</dc:date>
  <dc:description>This study evaluated the effects of dietary methylmercury (MeHg) on immune system development in captive-reared nestling American kestrels (&lt;i&gt;Falco sparverius&lt;/i&gt;) to determine whether T cell&amp;ndash;mediated and antibody-mediated adaptive immunity are targets for MeHg toxicity at environmentally relevant concentrations. Nestlings received various diets, including 0 (control), 0.6, and 3.9 &amp;mu;g/g (dry wt) MeHg for up to 18 d posthatch. Immunotoxicity endpoints included cell-mediated immunity (CMI) using the phytohemagglutinin (PHA) skin-swelling assay and antibody-mediated immune response via the sheep red blood cell (SRBC) hemagglutination assay. T cell&amp;ndash; and B cell&amp;ndash;dependent histological parameters in the spleen, thymus, and bursa of Fabricius were correlated with the functional assays. For nestlings in the 0.6 and 3.9 &amp;mu;g/g MeHg groups, CMI was suppressed by 73 and 62%, respectively, at 11 d of age. Results of this functional assay were correlated with T cell&amp;ndash;dependent components of the spleen and thymus. Dose-dependent lymphoid depletion in spleen tissue directly affected the proliferation of T-lymphocyte populations, insofar as lower stimulation indexes from the PHA assay occurred in nestlings with lower proportions of splenic white pulp and higher THg concentrations. Nestlings in the 3.9 &amp;mu;g/g group also exhibited lymphoid depletion and a lack of macrophage activity in the thymus. Methylmercury did not have a noticeable effect on antibody-mediated immune function or B cell&amp;ndash;dependent histological correlates. We conclude that T cell&amp;ndash;mediated immunosuppression is the primary target of MeHg toward adaptive immunity in developing kestrels. This study provides evidence that environmentally relevant concentrations of MeHg may compromise immunocompetence in a developing terrestrial predator and raises concern regarding the long-term health effects of kestrels that were exposed to dietary MeHg during early avian development.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>10.1002/etc.519</dc:identifier>
  <dc:language>en</dc:language>
  <dc:publisher>Society of Environmental Toxicology and Chemistry</dc:publisher>
  <dc:title>Toxic effects of dietary methylmercury on immune system development in nestling American kestrels (&lt;i&gt;Falco sparverius&lt;/i&gt;)</dc:title>
  <dc:type>article</dc:type>
</oai_dc:dc>