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Light and electron microscopic observations of sporogenesis in the myxosporida, <i>Ceratomyxa shasta</i> (Noble, 1950)
37
Citations
14
References
1979
Year
Molecular BiologyPathologyEmbryologyUnicellular OrganismElectron MicroscopyBiophysicsParasitologyParasitic ProtozoaMorphogenesisMicroscopic ObservationsEmbryonic DevelopmentOrganogenesisCeratomyxa ShastaBiologySpore BiologyDevelopmental BiologyNatural SciencesPathogenesisElectron MicroscopePhycologyMedicine
Abstract. The stages of development leading to sporogenesis of Ceratomyxa shasta (Noble) were investigated by light and electron microscopy. Salmonid fishes were infected by exposing them to water containing the infectious stage and intestinal material was fixed at weekly intervals. Signs of intestinal infection were barely detectable by 7 days following exposure where trophozoites and later developmental forms were present, but by 14 days a large number of pansporoblasts could be detected in varying stages of development. By 21 days the majority of caeca were completely occluded and infection had spread throughout the connective tissues attached to the caeca. The early developing trophozoites contained two or more nucleated cells within a mother cell. There was some evidence of multiplication of nuclei by fission. The sporoblasts usually contained twelve nucleated cells that gave rise to two groups of six cells (sporonts) and resulted in the formation of two spores in each mother cell. Each spore was formed by two sets of bilaterally arranged cells consisting of the main germinative cell or sporoplasm, the anteriorly placed capsule cells and the outer envelope or spore valve cell that surrounded the others and formed the spore covering. As the spore matured the two germinative cells interacted with each other by pseudopodial extensions and appeared to fuse to form a diploid cell. The position of the cells laterally and slightly posteriorly to the central suture line formed a bilaterally curved spore. Mature spores when examined with the electron microscope were condensed, dark staining and relatively featureless, with a lateral measurement of 15 μm and an anterior‐posterior measurement of 7μm.
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