Experimentally induced whirling disease ii. determination of longevity of the infective triactinomyxon stage of myxobolus cerebralis by vital staining

Journal of Aquatic Animal Health

Volumn 4, Issue 1, 1992, Pages 44-47

  Markjw, Maria E ^a  

^a LEETOWN SCIENCE CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0003047660     PISSN: 08997659     EISSN: 15488667     Source Type: Journal    
DOI: 10.1577/1548-8667(1992)004<0044:EIWDID>2.3.CO;2     Document Type: Article

References (7)

1. Jones, K. H., and J. A. Senft. 1985. An improved method to determine cell viability by simultaneous staining with fluorescein diacetate-propidium iodide. Journal of Histochemistry and Cytochemistry 33:77–79.
2. Lom, J. 1987. Myxosporea: a new look at long-known parasites of fish. Parasitology Today 3:327–332.
3. Markiw, M. E. 1986. Salmonid whirling disease: dynamics of experimental production of the infective stage–the triactinomyxon spore. Canadian Journal of Fisheries and Aquatic Sciences 43:521–526.
4. Markiw, M. E., and K. Wolf. 1974. Myxosoma cerebralis: isolation and concentration from fish skeletal elements–sequential enzymatic digestion and purification by differential centrifugation. Journal of the Fisheries Research Board of Canada 31:15–20.
5. Matyus, L., G. Shabo, I. Resli, and R. Gaspar. 1983. Flow cytometric analysis of viability of mammalian sperm cells. Acta Biochimica et Biophysica Academiae Scientianim Hungaricae 18:75.
6. Rotman, B., and B. W. Papermaster. 1966. Membrane properties of living mammalian cells as studied by enzymatic hydrolysis of fluorogenic esters. Proceedings of the National Academy of Sciences USA 55: 134–141.
7. Widholm, J. M. 1972. The use of fluorescein diacetate and phenosafranine for determining viability of cultured plant cells. Stain Technology 47:189–194.