Taylor L. Reynolds1; Salvatore Frasca, Jr.2; K. Spencer Russell2; Herbert E. Whiteley2; Sonia L. Mumford3
Abstract
Reports of cataracts in captive fish are plentiful, particularly in trout
and salmon. Formation of cataracts has been linked to nutritional
deficiencies11,10,4,17, rapid growth rates2,3, genetic
inheritance15, toxins8,9, infectious agents, osmotic stress, and excessive
exposure to ultraviolet (UV) radiation5,6,16,19. Retinal degeneration, in contrast,
has been documented infrequently and has been associated with genetically manipulated transgenic
zebrafish7,12 and celestial goldfish13,14, and with diabetes mellitus in
carp.18 Eight of 18 wild-caught juvenile Pollack (Pollachius virens) were
placed on display in a brightly lit tank at the National Marine Fisheries Service (NMFS)
Aquarium in Woods Hole, MA, and 10 were shipped to the New England Aquarium (NEA) in Boston, MA.
Six of the 10 pollack received by NEA were relocated to a dimly lit display tank, whereas 4 were
placed in a brightly lit, basin-like tank, in a Puffin display. Within 4 months, 5 of 6 pollack
in the dimly lit tank developed cataracts diagnosed by ophthalmoscopic examination. Affected
pollack grew increasingly unable to locate food, became emaciated, and were euthanized 5 months
after diagnosis. No gross lesions were identified in the coelomic viscera at necropsy
examination, and globes were immersion-fixed in Bouin's solution for routine paraffin embedding
and histopathologic examination. Subcapsular, cortical cataracts were found in 4 of 5 pollack,
and were bilateral in 3 and unilateral in 1 pollack. Marked to severe retinal degeneration and
atrophy was evident in 5 of these 5 pollack, the most severe degeneration being central rather
than peripheral. None of the other 12 pollack from the original cohort of 18 developed cataracts
clinically evident by ophthalmoscopic examination ante-mortem. However, upon histologic
examination, 4 of 5 pollack from the NMFS facility had mild, focal, subcapsular cataracts, 3
unilateral and 1 bilateral, and 1 had retinal degeneration comparable to that of the pollack
from NEA. In comparison, no microscopic lenticular or retinal lesions were identified in 5
wild-caught, adult pollack acquired from Connecticut fisherman and examined in the manner
previously described. To our knowledge, this is the first documentation of the combination of
cataract and retinal degeneration in a species of the family Gadidae. Differences in
environmental and husbandry factors exist between the two NEA tanks and the two aquaria to
provide clues as to the causative agent(s). Current investigations into the etiology are focused
on determining variations in UV light exposure and nutrition between the three aquarium
settings.
Acknowledgements
The authors acknowledge Tania Taranovski, Brandon Schmidt, and volunteers
of NEA for their care of pollack, for providing answers regarding the husbandry conditions, and
for assisting in medical examinations, euthanasia and necropsies of affected fish. We are
grateful to Kevin Dunn from the National Marine Fisheries Aquarium for donating 5 pollack for
this study and for supplying answers as to the husbandry conditions at the NMFS.
References
1. Barash H., H.A. Poston, and G.L. Rumsey. 1982. Differentiation
of soluble proteins in cataracts caused by deficiencies of methionine, riboflavin, or zinc in
diets fed to Atlantic Salmon, Salmo salar, Rainbow Trout, Salmo gairdneri, and
Lake Trout, Salvelinus namaycush. Comell Veterinarian 72:361-371.
2. Bijerkas E., et al. 1995. Cataracts in rapidly growing farm
raised Atlantic Salmon (Salmo salar), Veterinary Quarterly 17:1.
3. Bjerkas E., et al. 1996. Cataract development in Atlantic
Salmon (Salmo salar L) in fresh water, Acta. Vet. Scand. 37:351-360.
4. Cowey C.B., et al. 1992. Methionine intake in rainbow trout
(Oncorhynchus mykiss), relationship to cataract formation and the metabolism of
methionine, Journal of Nutrition 122:1154-1163.
5. Cullen A.P., and C.A. Monteith-McMaster. 1992. Damage to the
rainbow trout (Oncorhyncus mykiss) lens following an acute dose of UVB, Current Eye
Research 12, 97-106.
6. Cullen A.P., C.A. Monteith-McMaster, and J. G. Sivak. 1994.
Lenticular changes in rainbow trout following chronic exposure to UV radiation, Current Eye
Research 13:731-737.
7. Daly, F.J. and J.H. Sandell. 2000. Inherited retinal
degeneration and apoptosis in mutant Zebra fish, Anatomic Record 258:145-155.
8. Dobson, P. and Schuurman, H.J. 1990. Possible causes of
cataract in Atlantic Salmon (Salmo salar), Experimental Eye Research 50, 439-42.
9. Fraser, P.J.G. Duncan, and J. Tomlinson. 1990. Nuvan and
cataracts in Atlantic Salmon (Salmo salar), Experimental Eye Research 50, 443-447.
10. Hughes S.G., et al. 1981. Biomicroscope and histologic pathology of
the eye in riboflavin deficient rainbow trout (Salmo gairdneri), Comell Veterinarian
71:269-279.
11. Ketola H.G. 1979. Influence of Dietary Zinc on Cataracts in Rainbow
Trout (Salmo gairdneri.) Journal of Nutrition. 109:965-969.
12. Malicki, J., et al. 1996. Mutations affecting development of the
zebra fish retina, Development 123: 263-273.
13. Matsumura, M, et al. 1981. Electron microscopic studies on celestial
goldfish retina- a possible new type of retinal degeneration in experimental animals,
Experimental Eye Research 32, 649-656.
14. Matsumura, M., et al. 1982. Retinal degeneration in celestial
goldfish, Ophthalmic. Research 14:344-353.
15. Noga, E.J., E.D. Wolf, and P.T. Cardeilhac 1981. Cataracts in
Cichlid Fish, JAVMA 179:11:1181-1182.
16. Pitts, D,G., A.P. Cullen, and P.D. Hacker. 1977. Ocular effects of
near ultraviolet radiation: Literature Review, American Journal of Optometry & Physiological
Optics 54"8"542-549.
17. Richardson, N.L., et al. 1985. Influence of dietary calcium,
phosphorus, zinc and sodium phytate level on cataract incidence, growth and histopathology in
juvenile Chinook Salmon (Oncorhynchus tshawytscha), Journal of Nutrition 115:553-567.
18. Yokote, M. 1974. Spontaneous diabetes in carp (Cyprinus
carpio) Special Publications Japan Sea Fish Lab 67-74.
19. Zigman S., J. Schultz and T. Yulo. 1973. Possible roles of near UV
light in the cataractous process, Experimental Eye Research 15, 201-208.