Recent research indicates the fish immune system represents a highly sensitive target of immunotoxicant exposure. Further, fish appear to respond similarly to mammals following such immunotoxicant assault. These reports indicate that fish may represent a viable alternate species to mammals which can be employed for chemical immunotoxicity screening. The proposed studies will determine the ability of immune screens with demonstrated high predictive value for immunotoxicity (immunosuppression) in rodents to detect immunotoxicants in the tilapian fish species Oreochromis niloticus. Nine chemical agents with positive rodent immunotoxicity classification and five agents with negative rodent immunotoxicity classification will be evaluated using eight immune assays in tilapia. The immune screens to be evaluated in fish (and the estimated individual predictive value of each test for immunosuppression in rodents will include the: 1) spleen antibody plaque forming cell (PFC) assay [78%]; 2) natural killer (NK) cell cytotoxicity [69%]; 3) T cell lymphoproliferative responses [67%]; 4) spleen to body-weight ratio [61%]; 5) splenic cellularity [56%]; 6) mixed lymphocyte response [56]%; 7) B cell lymphoproliferative responses (50%]; and 8) peripheral leukocyte counts [43%]. The individual and pairwise concordance (e.g., sum of specificity and sensitivity, where sensitivity is the probability to predict an immunotoxicant with the immune assay given the compound is truly an immunotoxicant, and where specificity is the probability of correctly identifying non-immunotoxic chemicals using the immune assays) values of each of these immune tests to predict immunotoxic compounds in tilapia will then be calculated. The assimilated data from this project will determine for the first time the ability of immune screens with high predictive value in laboratory rodents to accurately identify chemical immunotoxicants in fish. In particular, the project will determine the potential for use of a fish species (tilapia) as an alternate to mammals for immunotoxicity screening, as well as the predictive value for immunotoxicity of the selected immune screens for a selected set of immunotoxicants in fish.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Research Project (R01)
Project #
5R01ES007612-03
Application #
2459010
Study Section
Special Emphasis Panel (SRC (R))
Project Start
1995-08-01
Project End
1998-07-31
Budget Start
1997-08-01
Budget End
1998-07-31
Support Year
3
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Virginia Polytechnic Institute and State University
Department
Veterinary Sciences
Type
Schools of Veterinary Medicine
DUNS #
003137015
City
Blacksburg
State
VA
Country
United States
Zip Code
24061
Carlson, D B; Williams, D E; Spitsbergen, J M et al. (2001) Fumonisin B1 promotes aflatoxin B1 and N-methyl-N'-nitro-nitrosoguanidine-initiated liver tumors in rainbow trout. Toxicol Appl Pharmacol 172:29-36
Gogal Jr, R M; Smith, B J; Kalnitsky, J et al. (2000) Analysis of apoptosis of lymphoid cells in fish exposed to immunotoxic compounds. Cytometry 39:310-8
Smith, D A; Schurig, G G; Smith, S A et al. (1999) Tilapia (Oreochromis niloticus) and rodents exhibit similar patterns of inhibited antibody production following exposure to immunotoxic chemicals. Vet Hum Toxicol 41:368-73
Orner, G A; Hendricks, J D; Arbogast, D et al. (1998) Modulation of aflatoxin-B1 hepatocarcinogenesis in trout by dehydroepiandrosterone: initiation/post-initiation and latency effects. Carcinogenesis 19:161-7
Holladay, S D; Smith, S A; Besteman, E G et al. (1998) Benzo[a]pyrene-induced hypocellularity of the pronephros in tilapia (Oreochromis niloticus) is accompanied by alterations in stromal and parenchymal cells and by enhanced immune cell apoptosis. Vet Immunol Immunopathol 64:69-82
Hart, L J; Smith, S A; Smith, B J et al. (1997) Exposure of tilapian fish to the pesticide lindane results in hypocellularity of the primary hematopoietic organ (pronephros) and the spleen without altering activity of phagocytic cells in these organs. Toxicology 118:211-21
Orner, G A; Hendricks, J D; Arbogast, D et al. (1996) Modulation of N-methyl-N'-nitro-nitrosoguanidine multiorgan carcinogenesis by dehydroepiandrosterone in rainbow trout. Toxicol Appl Pharmacol 141:548-54
Orner, G A; Donohoe, R M; Hendricks, J D et al. (1996) Comparison of the enhancing effects of dehydroepiandrosterone with the structural analog 16 alpha-fluoro-5-androsten-17-one on aflatoxin B1 hepatocarcinogenesis in rainbow trout. Fundam Appl Toxicol 34:132-40
Orner, G A; Mathews, C; Hendricks, J D et al. (1995) Dehydroepiandrosterone is a complete hepatocarcinogen and potent tumor promoter in the absence of peroxisome proliferation in rainbow trout. Carcinogenesis 16:2893-8
Kelly, J D; Orner, G A; Hendricks, J D et al. (1992) Dietary hydrogen peroxide enhances hepatocarcinogenesis in trout: correlation with 8-hydroxy-2'-deoxyguanosine levels in liver DNA. Carcinogenesis 13:1639-42