Myxozoans are cnidarian parasites of primarily freshwater and marine fish, with some being important pathogens of aquacultured fish species worldwide. Their life cycles have waterborne actinospores released from aquatic annelid definitive hosts and myxospore stages in fish intermediate hosts. In the southeastern United States, catfish aquaculture is burdened by annual losses to a myriad of infectious diseases. Henneguya ictaluri, the causative agent of proliferative gill disease in channel catfish Ictalurus punctatus and female channel catfish x male blue catfish Ictalurus furcatus hybrids, is the most commonly diagnosed parasitic disease of catfish in Mississippi. Other myxozoans infect these ictalurid fish, but their impact on catfish production is unknown. Surveys of actinospores from the oligochaete Dero digitata and myxospore stages from fish revealed an unexpected diversity for these production systems. Six genetically distinct actinospores representing four collective groups were observed from D. digitata. Herein, two novel Henneguya spp. are described from the gills and a novel Unicauda sp. is described from the intestinal tract of channel catfish. One Henneguya sp. was linked to its actinospore stage and represents the fourth known life-cycle in the genus. In addition to catfish, smallmouth buffalo Ictiobus bubalus polycultured with catfish were examined and two Myxobolus spp. were characterized from the gills. Phylogenetic analyses strongly support a clade of ictalurid Henneguya spp. and a clade of catostomid Myxobolus spp. Although diverse, H. ictaluri is the only myxozoan in catfish attributed to significant losses. With no feasible method of control or treatment, investigations into less susceptible fish were initiated and showed promise. Infectivity trials characterizing H. ictaluri development in channel, blue, and hybrid catfish were performed. Channel catfish were suitable hosts with myxospores developing in the gills by six weeks and persisting for at least 14 weeks. In hybrid catfish arrested or limited development was observed with no pseudocysts observed during Trial 1 and only two at 14 weeks during Trial 2. These results may suggest a possible way of decreasing losses attributed to PGD through hybrid catfish monoculture or fish crop rotation to reduce the number of infectious myxospores released into the pond.

Proliferative gill disease (PGD) caused by the myxozoan parasite Henneguya ictaluri is one of the most devastating parasitic infections in channel catfish aquaculture. Currently, there is no effective treatment for H. ictaluri and the unpredictable outbreaks can result in 100% mortality. Management strategies have been developed to prevent losses in newly stocked fingerlings by evaluating the PGD status of a pond prior to stocking, which is difficult since resident fish may not show clinical signs even when actinospore levels are lethal to naive fish. Current diagnostic methods are limited to the identification of an active infection and methods of predicting potential outbreaks have several limitations. The PGD status of a pond to be stocked can be determined using sentinel fish exposures which are labor intensive and require a source of parasite free fish. These limitations necessitated the development of more rapid and efficient means of determining actinospore concentrations to determine the risk of losing fish prior to stocking. The development of a quantitative real-time polymerase chain reaction (QPCR) assay provided a more rapid, sensitive and quantitative method of diagnosing active infections and also provides a means to predict potential PD outbreaks and determine the PGD status of a pond prior to stocking. Another approach in the control of this parasite is the identification of a less susceptible culturable species or to identify traits that could be targeted in a selective breeding program. Challenge studies have shown that the closely related blue catfish (Ictalurus furcatus) does not exhibit as severe an inflammatory response to H. ictaluri and mortalities are significantly lower than in channel catfish. Comparisons of PGD severity and H. ictaluri infection in channel catfish, blue catfish and channel x blue catfish backcross hybrids by gross examination, histopathology and the newly developed H. ictaluri real-time PCR (QPCR) assay supported previous research suggesting the life cycle of the parasite can not be completed as efficiently through the blue catfish host. This dissertation describes the development and validation of a QPCR assay to detect H. ictaluri in both fish tissues and environmental samples and the application of this assay in both research and production settings.