A capillary tube holder, devised to minimize shadow effects during microscopic examination of haematocrit capillary tubes for trypanosomes, is described. A blood dispenser, designed to remove trypanosomes from centrifuged tubes, resulted in thinner smears of trypanosomes covering a smaller area. The anterior end of centrifuged trypanosomes was abnormally thickened and the kinetoplast displaced posteriorly.
The present communication reports on the attenuation of a pathogenic hemoflagellate, Cryptobia salmositica Katz (Sarcomastigophora: Kinetoplastida) and its use as a live vaccine against cryptobiosis. The parasite was attenuated by continuous in vitro culture (at 10 C for 55 wk) in minimum essential medium. Attenuated (culture) forms are morphologically similar to virulent (blood) forms. They are however more slender and have a shorter anterior flagellum and a smaller nucleus and kinetoplast. The attenuated form returned to its normal size and multiplied when inoculated into naive Oncorhynchus mykiss. It produced a low parasitemia but did not cause disease (e.g., no exophthalmia or anemia) in fish. At four wk after infection, the vaccinated fish were challenged with the virulent parasite. They were protected from the disease, whereas the control (naive) fish, infected with only the virulent parasite, had the usual clinical signs (e.g., anemia, exophthalmia). No parasite was detected in any of 10 vaccinated fish at 22 wk after challenge with the virulent parasite. However, 5 of 9 fish infected with culture forms and 6 of 9 fish infected with blood forms still had detectable parasites at 26 and 22 wk after infection, respectively.
A review on the history, classification, genetic characteristics, geographic distribution, host range, environmental impact, diagnosis, epidemiology, treatment and control of bacterial kidney disease caused by Renibacterium salmoninarum was presented.
Natural anti-proteases (alpha 1-protease inhibitor (alpha 1-PI; alpha 1-antitrypsin) and alpha 2-macroglobulin (alpha 2-M)) were found in the blood of rainbow trout, Oncorhynchus mykiss and brook charr, Salvelinus fontinalis. The alpha 2-M inhibited Cryptobia salmositica proteases and was significantly higher in brook charr than in rainbow trout. Under in vitro conditions it took longer for the same number of parasites to neutralize the alpha 2-M in charr than in trout blood. The haemolysis which occurred when C. salmositica was incubated in the blood of rainbow trout was due to neutralization of alpha 2-M. This in vitro study also showed that it was the metalloprotease of C. salmositica that lysed red blood cells and the plasma of the two species of fishes initially prevented haemolysis by inhibiting the proteolytic activity. We suggest that the natural plasma alpha 2-M plays an important role in defence against cryptobiosis in fishes.
The aetiology, clinical aspects, geographical distribution and host range, epidemiology, economic importance, taxonomic classification, serology, physicochemical properties, genetic analysis, diagnosis and diagnostic techniques, pathogenesis, immune mechanism, outbreaks, predisposing factors, transmission, prevention and control of Infectious pancreatic necrosis and associated aquatic birnaviruses were discussed. Conclusions and recommendations for future studies were also presented in this chapter.
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