Immunological evaluation of captive green sea turtle (Chelonia mydas) with ulcerative dermatitis.

Ulcerative dermatitis (UD) is common in captive sea turtles and manifests as skin erosions and ulcers associated with gram-negative bacteria. This study compared clinically healthy and UD-affected captive turtles by evaluating hematology, histopathology, immunoglobulin levels, and delayed-type hypersensitivity assay. Turtles with UD had significantly lower weight, reduced delayed-type hypersensitivity (DTH) responses, and higher heterophil:lymphocyte ratios. This study is the first to assay DTH in green turtles (Chelonia mydas) and suggests that UD is associated with immunosuppression.

Organohalogen contaminants in blood of Kemp's ridley (Lepidochelys kempii) and green sea turtles (Chelonia mydas) from the Gulf of Mexico.

The threat that exposure to organohalogen (OH) contaminants poses to endangered populations of Kemp's ridley (Lepidochelys kempii) and green sea turtles (Chelonia mydas) is not well understood, partly because few OH data are available. Blood samples from live juvenile and sub-adult L. kempii (n = 46) and C. mydas (n = 9) from the Gulf of Mexico and from L. kempii from the southeastern US coast (n = 3) were extracted using microwave-assisted extraction, and analyzed by large volume injection gas chromatography-mass spectrometry for 85 polychlorinated biphenyls (PCBs), 25 organochlorine pesticides (OCPs) and 27 polybrominated diphenyl ethers (PBDEs). Plasma chemistries, hematology and immune responses were also assessed. Concentrations of SigmaPCBs (geometric mean, range: 3190 pg g(-1), 227-21590 pg g(-1) blood), SigmaDDTs (geometric mean, range: 541 pg g(-1), 161-4310 pg g(-1) blood) and OCPs in L. kempii from the Gulf were comparable to those reported in L. kempii from the Atlantic. SigmaPBDEs were detected in all samples (geometric mean, range: 146 pg g(-1), 19.5-1450 pg g(-1) blood), with PBDE 47, 99, 100, 153 and 154 being the predominant congeners. SigmaPCBs, SigmaDDTs and Sigmachlordanes were one order of magnitude lower in green turtles, and SigmaPBDE concentrations were lower by half due to trophic level differences. L. kempii from the southeast USA had higher percentages of highly chlorinated PCBs indicating exposure to Aroclor 1268. Blood urea nitrogen was positively correlated to Sigmachlordanes, and SigmaPCBs were inversely correlated to creatine phosphokinase in L. kempii. These data help establish baseline contaminant concentrations in live L. kempii and C. mydas.

Identification of CD3+ T lymphocytes in the green turtle Chelonia mydas.

To understand the role of the immune system with respect to disease in reptiles, there is the need to develop tools to assess the host's immune response. An important tool is the development of molecular markers to identify immune cells, and these are limited for reptiles. We developed a technique for the cryopreservation of peripheral blood mononuclear cells and showed that a commercially available anti-CD3 epsilon chain antibody detects a subpopulation of CD3 positive peripheral blood lymphocytes in the marine turtle Chelonia mydas. In the thymus and in skin inoculated with phytohemagglutinin, the same antibody showed the classical staining pattern observed in mammals and birds. For Western blot, the anti-CD3 antibodies identified a 17.6k Da band in membrane proteins of peripheral blood mononuclear cell compatible in weight to previously described CD3 molecules. This is the first demonstration of CD3+ cells in reptiles using specific antibodies.