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The public health importance of Kudoa infection in fish remains unclear. Recently in Japan a Kudoa species, K. septempunctata, was newly implicated as a causative agent of unidentified food poisoning related to the consumption of raw olive flounder. Other marine fishery products are also suspected as causative raw foods of unidentified food poisoning. For this study, we detected kudoid parasites from sliced raw muscle tissues of a young Pacific bluefin and an adult yellowfin tuna. No cyst or pseudocyst was evident in muscles macroscopically, but pseudocysts were detected in both samples histologically. One substitution (within 1100 bp overlap) and ten substitutions (within 753 bp overlap) were found respectively between the partial sequences of 18S and 28S rDNAs from both isolates. Nucleotide sequence similarity searching of 18S and 28S rDNAs from both isolates showed the highest identity with those of K. neothunni from tuna. Based on the spore morphology, the mode of parasitism, and the nucleotide sequence similarity, these isolates from a Pacific bluefin and a yellowfin tuna were identified as K. neothunni. Phylogenetic analysis of the 28S rDNA sequence revealed that K. neothunni is classifiable into two genotypes: one from Pacific bluefin and the other from yellowfin tuna. Recently, an unidentified kudoid parasite morphologically and genetically similar K. neothunni were detected from stocked tuna samples in unidentified food poisoning cases in Japan. The possibility exists that K. neothunni, especially from the Pacific bluefin tuna, causes food poisoning, as does K. septempunctata.
Glycogen phosphorylase activity was measured in extracts from muscles isolated from a number of body fragments of Ascaris suum females. The highest total activity of the enzyme was recorded in muscles located near the vulva, whereas the lowest activity was found in those from the head and the tail region. No statistically significant differences in the enzyme activity were found between muscles from dorsal and ventral body fragments. The activity of phosphorylase a predominated in muscles from the tail region, whereas that of phosphorylase b predominated in the remaining fragments of the nematode body. The distribution of maxima and minima of total muscle phosphorylase activity along the body of A. suum was opposite to these of α-amylase, thus supporting the view on mutual competition between the glycogenolytic and the amylolytic pathway of glycogen degradation.
Ultrastructural characteristics of developing eggs in the late preoncospheral and oncospheral stage and that of the uterine capsules in the hymenolepidid cestode, Pseudhymenolepis redonica Joyeux et Baer, 1935, are described. The uterus in this species breaks down very early into uniovular capsules. The uterine wall consisted of a syncytial flat uterine epithelium separated from the medullary parenchyma by a thin extracellular basal matrix. The uterine epithelium contained elongated nuclei with prominent nucleoli in the juxtalumenal cytoplasm. Its apical plasma membrane was folded into long microlamellae. The differentiating and mature oncosphere were surrounded by three envelopes: (1) an outer envelope, still containing the nuclei in the preoncospheral stage; (2) an inner envelope consisting of three layers - an extraembryophoral cytoplasmic layer, a thin and discontinuous embryophore, and intraembryophoral cytoplasmic layer; (3) a thin oncospheral membrane, closely surrounding the oncosphere. The relative thickness of the extraembryophoral and intraembryophoral layers of the inner envelope was changing during egg maturation. The numerous small mitochondria which were initially present only in the intraembryophoral layer, were concentrated later in the extraembryophoral layer and in many cases were observed in the embryophoral pores. The above data may suggest that these cytoplasmic organelles are pushed through the embryophoral pores as a result of the pressure of the developing oncosphere. The oncosphere surface was covered by the cytoplasmic oncospheral tegument, basal lamina and a layer of subtegumental somatic muscles. Several cell types were distinguished in the differentiating and mature oncospheres, namely: the germinative cells; somatic cells (= myocytons of somatic and hook muscles); the bi-lobed penetration gland with its secretory granules; the “neurosecretory” cells with their characteristic dense-cored membrane-bound vesicles. Each oncosphere had three pairs of embryonic hooks: one median, one dorso-lateral and one ventro-lateral pair. The degenerating hook-forming cells or oncoblasts remained visible around the hook handles. The details of the ultrastructure of the uterine capsules, oncospheral envelopes and different cell types of differentiating and mature oncospheres of P. redonica are discussed in comparison with literature data on other hymenolepidids, parasites of mammals and birds.
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