Histochemical studies of enzyme activities and structural elements in Gyrodactylus derjavini Mikailov, 1975 parasitizing fins of Oncorhynchus mykiss Walbaum were conducted. Marked activities of non-specific esterase, acid phosphatase, alkaline phosphatase and amino-peptidase were found in the intestinal caeca of the parasite. A strong activity of acetylcholinesterase was seen in the nervous system. Extraintestinal non-specific and eserine-sulphate resistant esterase was localized in the distal part of the hamulus sheath. Activities of peroxidase and glucuronidase were not detected. In the embryo, developing hamuli were enclosed in a sheath rich in phospholipids. Deposits of neutral lipids were sparse. The fully developed ventral and dorsal hamulus bars stained strongly for calcium. Lectin binding assays showed a mannose rich region in the cephalic duct openings, strong reactions for galactose in the glycocalyx whereas reactions for lactose were weak. These findings arc discussed with respect to the parasite-host relationship.
Microhabitat preference of the monogenean Discocotyle sagittata (Leuckart, 1842) was determined in late spring and late autumn in rainbow trout, Oncorhynchus mykiss (Walbaum), reared in the Isle of Man, UK. Discocotyle sagittata exhibits a preference for attachment to anterior gill arches: 29% of all worms occurred on gill arch I, 28% on II, 25% on III and 18% on IV. This distribution pattern on the introduced salmonid species is the same as reported for its native European host, the brown trout Salmo trutta (L.). Previous experimental work suggested that invasion is a passive process followed by post-invasion migration to anterior gill arches; the present work provides evidence of equivalent site selection taking place in fishes maintained under conditions promoting continuous reinfection in aquaculture. Migration may be density-dependent, since a significant inverse association was found between the intensity of mature parasites and their proportion on anteriormost gill arch I.
We studied amoebae associated with nodular gill disease (NGD) outbreaks in rainbow trout Oncorhynchus mykiss (Walbaum) in fish farms in South-Western Germany. Gills of 12 diseased rainbow trout were examined in fresh, by isolation attempts, histologically and using in situ hybridisation (ISH). A total of nine amoeba strains of the genera Acanthamoeba (1), Hartmannella (2), Naegleria (1), Protacanthamoeba (1) and Vannella (4) were isolated and determined using light microscopical, ultrastructural and molecular methods. Specific molecular probes designed from the SSU rDNA sequences of individual amoeba strains were used for non-radioactive ISH in histological sections. Association of Naegleria sp. with NGD and a direct ISH proof of Naegleria trophozoites attached to hyperplastic gill epithelium are novel findings, expanding the number of possible agents of NGD and supporting the hypothesis on multicausal aetiology of this disease.
The aim of this study was to investigate the post-cyclic transmission of Acanthocephalus tumescens (von Linstow, 1896) from Galaxias maculatus Jenyns to Oncorhynchus mykiss (Walbaum). Wild G. maculatus naturally infected with A. tumescens were fed to cultured rainbow trout, which were sacrificed at the second, third and fourth weeks post infection. Normally attached male and female acanthocephalans were recovered alive from the intestine of rainbow trout. Parasites survive at least four weeks post infection, growing and attaining full sexual maturity. Prevalence and mean intensity generally decreased after infection. A. tumescens is the eighth acanthocephalan species in which post-cyclic transmission has been proven.
Loma salmonae (Putz, Hoffman et Dunbar, 1965) is a common gill parasite of salmonids, and essentially all species in the genus Oncorhynchus are susceptible. Infections occur in both fresh and salt water. Loma salmonae is directly transmissible by ingestion of spores or infected tissue. The parasite infects the wall of blood vessels of various organs, but the gill is the primary site of infection. Initial infection occurs in the intestine, and xenomas are easily detected in the gills by standard histology at 4-6 wk post-exposure. A few presporogonic stages of the parasite are found in the heart endothelium prior to xenoma formation in the gills. Ultrastructure studies of early infections demonstrated that wandering blood cells transport the meronts to the gills, and that merogony occurs in pillar cells and other cells underlying the gill endothelium. Xenomas develop in these cells, resulting in hypertrophied host cells filled with spores. Xenomas ultimately rupture, and are associated with severe inflammation in which free spores are found in macrophages. The parasites are most pathogenic during this phase of the infection, resulting in severe vasculitis and clinical disease. Both rainbow trout (Oncorhynchus mykiss) and Chinook salmon (Oncorhynchus tshawytscha) recover from infections, but free spores persist in kidney and spleen phagocytes for many months after xenomas are absent in Chinook salmon. Fish that have recovered from the infection show strong immunity against the parasite, lasting up to 1 year. Fish are susceptible to infection by other routes of exposure by spores; co-habitation, anal gavage, and intramuscular, intraperitoneal and intravascular injection. Autoinfection probably occurs following release of spores in blood vessels after xenomas rupture. The optimal temperature for L. salmonae infections is 15-17°C, with a permissive range of 11-20°C.
Experimental infection of rainbow trout Oncorhynchus mykiss (Walbaum) with the monogenean Discocotyle sagittata (Leuckart, 1842) allowed comparison between trickle and single exposure, two infection modes demonstrated to occur in the wild. Both types of infection resulted in mean larval attachment success around 50%, which was significantly dependent on dose of infective larvae used (P < 0.0001), but was not affected by mode of infection (P = 0.244). Worms recovered from fish exposed to the same number of oncomiracidia but different mode of infection differed in their rate of development. The developmental stage attained by parasites was significantly affected by number of infective larvae used (P = 0.005), and by the interaction between dose and mode of infection (P = 0.026), suggesting competition among attached larvae. Statistical analysis demonstrated that in the early stages of infestation, worm distribution over the gill arches can be explained by the relative amount of water flowing over them. One, two and three months post-infection parasite numbers were comparable (P = 0.805), but their observed distribution gradually decreased in gill arches III and IV and increased in gill arch I, suggesting that parasites migrate after initial attachment. These results reproduce phenomena observed in the field, indicating that the experimental infection system could be employed to study infection dynamics and host-parasite interactions under controlled conditions.