Search

A new species of Myxosporea, Myxobolus neurotropus n. sp., is described from the brain and spinal cord of rainbow trout (Oncorhynchus mykiss) from Duncan Creek, Owyhee County, Idaho. Spores are oval, have 2 pyriform polar capsules, and possess a thick spore wall (sutural rim) with a short intracapsular offshoot. The mean spore dimensions are length 11.8 microm, width 10.8 microm, and thickness 8.8 microm. This myxozoan is compared to other described Myxobolus species found in cranial tissues of salmonids in terms of spore morphology and phylogenetic analysis. Because it is found in brain and spinal cord, it is encountered while performing screening tests for Myxobolus cerebralis, the causative agent of salmonid whirling disease. Where chronic inflammation and granulomatous lesions are associated with M. cerebralis, histological examination shows no host response to M. neurotropus n. sp. A diagnostic polymerase chain reaction (PCR) test is included as an aid in properly identifying the species.

Henneguya gurlei was isolated from Ameiurus nebulosus captured in North Carolina and redescribed using critical morphological features and 18S small-subunit ribosomal RNA (SSU rDNA) gene sequence. Plasmodia are white, spherical, or subspherical, occur in clusters, measure up to 1.8 mm in length, and are located on the dorsal, pectoral, and anal fins. Histologically, plasmodia are located in the dermis and subdermally, and the larger cysts disrupt the melanocyte pigment layer. The spore body is lanceolate, 18.2 +/- 0.3 microm (range 15.7-20.3) in length, and 5.4 +/- 0.1 microm (range 3.8-6.1) in width in valvular view. The caudal appendages are 41.1 +/- 1.1 microm (range 34.0-49.7) in length. Polar capsules are pyriform and of unequal size. The longer polar capsule measures 6.2 +/- 0.1 microm (range 5.48-7.06), while the shorter is 5.7 +/- 0.1 microm (range 4.8-6.4) in length. Polar capsule width is 1.2 +/- 0.03 microm (range 1.0-1.54). The total length of the spore is 60.9 +/- 1.2 microm (range 48.7-68.5). Morphologically, this species is similar to other species of Henneguya that are known to infect ictalurids. Based on SSU rDNA sequences, this species is most closely related to H. exilis and H. ictaluri, which infect Ictalurus punctatus.

The myxozoan genus Davisia Laird 1953 is preoccupied by Davisia Del Guercio 1909 (Insecta: Hemiptera). Here, Myxodavisia nomen novum is proposed to replace the preoccupied name, and a new species is described. Myxodavisia sebastisca n. sp. was found in the urinary bladder of Sebastiscus marmoratus, collected from coastal waters off Xiamen in the East China Sea. The parasite is characterized by a disporous trophozoite; spherical to subspherical spore, 13.1 +/- 0.3 (12.7-13.6) by 12.3 +/- 0.9 (10.9-13.5) microm in size; curved sutural line; 2 shell valves each with a long lateral appendage 119.4-335.2 microm in length; and 2 spherical or subspherical polar capsules, equal in size, 4.6 +/- 0.6 (3.2-4.6) microm in diameter. Traditionally, Myxodavisia is distinguished from Ceratomyxa, Sinuolinea, and Sphaerospora spp. by having spores that possess a distinct central chamber and lateral appendages. A review of the literature reveals that the presence or absence of a clear septum between these spore components is open to interpretation. Indeed, in immature spores of M. sebastisca n. sp., there was an indication of a demarcated appendage, but in some mature spores, no clear separation was apparent. Our findings suggest that future revision of this genus is warranted, particularly once DNA sequence data become available.

The myxozoans Gadimyxa atlantica n. sp. and G. sphaerica n. sp., and G. arctica n. sp. (Myxozoa, Parvicapsulidae), are described from Gadus morhua L. and Arctogadus glacialis (Peters) (Gadidae), respectively. They develop coelozoic in bisporic plasmodia in the urinary systems. Two morphological forms of spores were found in all 3 species, i.e., wide and (sub)spherical forms. Both spore types are bilaterally symmetrical along the suture line. The wide spores, semicircular in frontal view and elliptical in apical view, have 2 spherical polar capsules, which open in the sutural or median plane mid on the flat side of the spore. Mean widths of the wide spores of G. atlantica, G. sphaerica, and G. arctica are 7.5, 10.0, and 10.0 microm, respectively. The older, more thick-walled, (sub)spherical spores with binucleate sporoplasm are 8.0, 5.3, and 7.3 microm in mean width, respectively. The mean diameters of the polar capsules of (sub)spherical spores are 2.4, 1.7, and 2.2 microm, respectively. The (sub)spherical forms of Gadimyxa are most similar to Ortholinea within the Ortholineidae, but they differ in the development of the spores and in the arrangement of the polar capsules. The polychaetes Spirorbis spp. (Spirorbidae) act as invertebrate hosts of G. atlantica. The previously described actinospores of the tetractinomyxon type develop to myxospores in Gadus morhua within 8 wk. This is the second known myxozoan 2-host life cycle in the marine environment. Phylogenetic analyses based on partial small subunit rDNA sequences places Gadimyxa spp. among Parvicapsula spp. in the Parvicapsulidae.

The infection of Myxobolus galaxii Szidat, 1953, from the musculature and abdominal organs of northwestern Patagonian Galaxias maculatus is described. Plasmodia are histozoic and intercellular. Spores are pyriform in valvar view and biconvex in sutural view, with 4-9 edge notches in the sutural line, varying in shape within the same plasmodium. Myxobolus galaxii was detected in fish from 7 of 17 Andean Patagonian lakes, with prevalences ranging between 2 and 17%. A repeating pattern of summer increment in prevalence was observed, which could be explained by the ontogenetic migratory movements of the fish in Lake Gutiérrez. Also, accumulation of plasmodia through the life span of fish was detected.

Myxospores consistent with species of Parvicapsula were observed in kidney of 15 of 95 (15.8%) adult pink salmon, Oncorhynchus gorbuscha, collected from the Quinsam River, British Columbia, Canada. The spores were elongate and curved with unequal valves, and 2 spherical-to-subspherical polar capsules within a highly refractile capsular region. The spores were unlike those of P. minibicornis found in nearby populations of Pacific salmon, Oncorhynchus spp. The spore dimensions were similar to those of Parvicapsula pseudobranchicola from Atlantic salmon, Salmo salar, in Norway, and the spores seemed similar to an undescribed Parvicapsula sp. from several Oncorhynchus spp. in Puget Sound, Washington. A sequence of 1,480 base pairs (bp) of the small subunit ribosomal RNA gene (SSU rDNA) of the parasite from pink salmon was most similar to, but distinct from, that of other Parvicapsula spp. The parasite is described as a new species, Parvicapsula kabatai n. sp. Polymerase chain reactions amplified a 158-bp sequence, unique to P. kabatai n. sp., from 22 of 93 (23.7%) adult pink salmon kidney samples, from 3 of 3 juvenile pink salmon collected in the ocean 125 km north of the Quinsam River, and from 2 of 5 archival coho salmon, Oncorhynchus kisutch, samples from Puget Sound. The parasite occurs within the lumen and epithelium of renal tubules and ducts, and within the renal interstitium. Concurrent infections with extrasporogonic stages of the myxosporean CKX, the microsporidian Loma salmonae, and a Myxidium sp. also were observed in the adult pink salmon.

Proliferative kidney disease (PKD), caused by the malacosporean parasite, Tetracapsuloides bryosalmonae, is a major disease of salmonid culture both in western Europe and North America. The fish are infected from spores that develop within freshwater bryozoans and are released into the water column. Although sporogenesis has been studied in the bryozoan host and occurs within sacs, the formation of these sacs from presaccular stages has only been hypothesized. Examination of infected bryozoans by using a range of techniques identified proliferating, presaccular amoeboid stages of T. bryosalmonae on the body wall of the bryozoan Fredericella sultana. These stages possessed unique electron-dense bodies and were observed as aggregating within the bryozoan metacoel, differentiating to form spore sacs. Spore sac growth was associated with the assimilation of the presaccular parasites rather than through cryptomitosis of sac mural cells. This sac formation through aggregation and assimilation suggests an intriguing mechanism by which T. bryosalmonae can cross-fertilize.

Myxobolus metynnis n. sp. (Phylum Myxozoa) is described in the connective subcutaneous tissues of the orbicular region of the fish, Metynnis argenteus (Characidae), collected in the lower Amazon River, near the city of Peixe Boi, Pará State, Brazil. Polysporic, histozoic plasmodia were delimited by a double membrane with numerous microvilli on the peripheral cytoplasm. Several life-cycle stages, including mature spores, were observed. An envelope formed by numerous fine and anastomosed microfibrils was observed at the spore surface. The spore body presented an ellipsoidal shape and was about 13.1 microm long, 7.8 microm wide, and 3.9 microm thick. Elongated-pyriform polar capsules were of equal size, measuring 5.2 microm in length, 3.2 microm in width, and possessing a polar filament with 8-9 turns around the longitudinal axis. The binucleated sporoplasm contained a vacuole and numerous sporoplasmosomes. These were circular in cross-section, showing an adherent eccentric, dense structure, with a half-crescent section. Based on the morphological differences and host specificity, we propose that the parasite is a new species named Myxobolus metynnis n. sp.

During March 2001-April 2004, 164 adult anurans of 6 species (47 Rana blairi, 35 Rana catesbeiana, 31 Hyla chrysoscelis, 31 Pseudacris triseriata triseriata, 11 Bufo woodhousii, and 9 Acris crepitans blanchardi) from Pawnee Lake, Lancaster County, Nebraska, were surveyed for myxozoan parasites. Of these, 20 of 31 (65%) P. triseriata triseriata and 1 of 9 (11%) A. crepitans blanchardi were infected with a new species of Myxidium. Myxidium melleni n. sp. (Myxosporea) is described from the gallbladder of the western chorus frog, P. triseriata triseriata (Hylidae). This is the second species of Myxidium described from North American amphibians. Mature plasmodia are disc-shaped or elliptical 691 (400-1,375) x 499 (230-1,200) x 23 (16-35) microm, polysporic, producing many disporic pansporoblasts. The mature spores, 12.3 (12.0-13.5) x 7.6 (7.0-9.0) x 6.6 (6.0-8.0) microm, containing a single binucleated sporoplasm, are broadly elliptical, with 2-5 transverse grooves on each valve, and contain 2 equal polar capsules 5.2 (4.8-5.5) x 4.2 (3.8-4.5) microm positioned at opposite ends of the spore. Myxidium melleni n. sp. is morphologically consistent with other members of Myxidium. However, M. melleni n. sp. was phylogenetically distinct from other Myxidium species for which DNA sequences are available. Only with improved morphological analyses, accompanied by molecular data, and the deposit of type specimens, can the ambiguous nature of Myxidium be resolved. Guidelines for descriptions of new species of Myxidium are provided.

Membership and richness of infracommunities and component communities of myxozoan fauna of the banded killifish (Fundulus diaphanus) from freshwater localities in Ontario, Quebec, New York State, New Brunswick, Nova Scotia, and Maryland were studied. Five species of parasites were found: Myxobolus diaphanus (Fantham, Porter, and Richardson, 1940) (connective tissue throughout the body and head), Myxobolus funduli (Kudo, 1918) (interlamellar), Myxobolus neurophilus (Guilford, 1963) (optic tectum of the brain), Myxobolus sp. (connective tissue, typically adjacent to vertebrae), and Sphaerospora sp. (kidney tubules). The most abundant species locally and regionally was M. diaphanus, occurring at prevalences of 14.2 to 93.3% at 6 of 9 localities. Myxobolus funduli and Myxobolus sp. were at 3 and 2 localities respectively, while M. neurophilus and Sphaerospora each occurred at single localities. Four of the 5 myxozoans appear to be specific to fundulids, the exception being M. neurophilus, which is typically a parasite of Perca flavescens. Mean infracommunity richness was 0-1.2. Component community richness was 0-3 species. The fauna is similar in composition to that described from the spottail shiner (Notropis hudsonius) in the Great Lakes in being dominated by histozoic myxobolids and in having maximum prevalence at any single locality correlate positively with geographical distribution. Moreover, mean infracommunity richness was correlated with percentage of hosts infected with any species at a locality, and maximum infracommunity richness was correlated with component community richness. Probably because fewer species of myxozoans of fundulids occur in the regional pool, myxozoan communities encountered in the present study are generally less rich than those described from N. hudsonius. It appears that dispersal of relatively resilient myxospores through such a mechanism as piscivory effectively distributes these parasites over the landscape, while the more delicate actinospores serve to ensure colonization by amplifying species' prevalence at a specific locality and thereby contributing to initial establishment. As such, these types of myxozoans, though they are autogenic, having their entire life cycle normally completed within the aquatic environment, behave more like allogenic parasites that rely on birds and mammals as definitive hosts.

Three new species of Kudoa, each having 6 polar capsules, are described from the somatic muscle of fishes collected on the Great Barrier Reef, Queensland, Australia. Kudoa grammatorcyni n. sp. was observed in the shark mackerel Grammatorcynus bicarinatus. Spores are stellate in apical view, width (all measurements in microm) 8.62 (8.03-8.95); thickness 8.14 (7.63-8.68); suture width 7.7 (7.24-8.16); length 6.54 (6.32-6.71); polar capsule length 3.68 (3.55-3.82); polar capsule width 1.72 (1.65-1.84). Kudoa scomberomori n. sp. is described from the Spanish mackerel Scomberomorus commerson. Spores are stellate in apical view, width 7.56 (6.84-8.16); thickness 6.79 (6.18-7.63); suture width 5.92 (5.26-6.32); length 5.43 (5.00-6.18); polar capsule length 3.24 (3.03-3.55); polar capsule width 1.37 (1.25-1.51). Kudoa thalassomi n. sp. is described from the moon wrasse Thalassoma lunare. Spores are stellate in apical view, width 10.66 (9.47-11.84); thickness 9.37 (8.55-10.79); suture width 7.98 (6.84-8.82); length 6.65 (6.18-7.11); polar capsule length 4.92 (4.74-5.00); polar capsule width 2.12 (2.04-2.24). All 3 species differ in spore morphology from the 1 previously described myxozoan with 6 polar capsules, Hexacapsula neothunni from yellowfin tuna Neothunnus macropterus, which has since been reassigned to Kudoa.

Postmortem myoliquefaction associated with multivalvulid myxozoans was found in fillets of red barracuda (Sphyraena pinguis) and splendid alfonso (Beryx splendens), which were imported to Japan from China and South Africa, respectively. Morphological examinations of the myxozoans from the somatic muscle of red barracuda revealed that spores (30.3-44.7 microm in maximum thickness) had 4 distinct winglike valves, in which 1 extremely large (12.7 x 5.8 microm), 2 small, and 1 vestigial polar capsule were present. The small subunit ribosomal DNA sequence analysis showed that the myxozoan cluster within a clade was composed of Kudoa thyrsites, Kudoa minithyrsites, and Kudoa lateolabracis, all having stellate spores with 1 polar capsule larger than the other 3. On the basis of these characteristics, we describe this parasite as Kudoa megacapsula n. sp. Morphological and molecular analyses of the myxozoan from splendid alfonso identified it as K. thyrsites, which has been described from many marine fishes. To our knowledge, this is the first record of K. thyrsites in splendid alfonso.

Gilt-head sea bream, Sparus aurata L., the Mediterranean's most important mariculture species, has been cultured for the last 30 yr in Eilat (Israeli Red Sea). Kudoa sp. was the first myxosporean parasite reported from this species. In recent years, an increase in prevalence in both land-based and sea-cage facilities in Eilat has been observed. Infections with the same Kudoa species appeared in cultured European sea bass Dicentrarchus labrax (L.) and grey mullet Mugil cephalus in the same farms, as well as in 10 species of wild Red Sea reef fish, indicating that Kudoa sp. is not fastidious with regard to its host. All affected species displayed 1- to 2-mm (up to 5 mm) whitish, spherical, or oval polysporous plasmodia. The parasite established multiple site infections, most commonly in the muscles and intracranial adipose tissue of the brain and eye periphery. Other sites were subcutaneous adipose tissue, nerve axons, mouth, eye, mesenteries, peritoneum, swim bladder, intestinal musculature, heart, pericardium, kidney, and ovary. On the basis of spore morphology, the parasite was identified as Kudoa iwatai Egusa and Shiomitsu, 1983. Ultrastructural features were comparable to those of previously studied Kudoa species. The 18S rDNA from 7 Red Sea isolates was sequenced and compared with the sequence of the same gene from K. iwatai isolated from cultured red sea bream, Pagrus major, in Japan. The phylogenetic position of K. iwatai within the genus was determined using sequence analysis of all related taxa available in GenBank. The 3 isolates of K. iwatai clustered together on a newly formed, highly supported clade. The Red Sea strain of K. iwatai is apparently native to the region. In the absence of records of this Kudoa sp. from the extensive Mediterranean sea bream and sea bass production industries, introduction with its Mediterranean hosts seems unlikely. Therefore, we conclude that K. iwatai is an Indo-Pacific species that, in the Red Sea, has extended its host range to include the allochthonous gilt-head sea bream, European sea bass, and grey mullet.

Spores of Myxobolus pendula develop within the cores of complex cysts on the gill arch of creek chub Semotilus atromaculatus. Adjacent to, and surrounding, the spores are concentric layers of stratified interdigitating cells, whose nature was examined by transmission electron microscopy and by immunohistochemical and molecular biological techniques. In situ hybridization data using parasite-derived ribosomal DNA as a probe indicate that infection leads to the encapsulation of developing plasmodia by host immune cells that form an epithelioid granuloma. Epithelioid cell-cell adhesion is effected by desmosomes anchored intracellularly to cytokeratin intermediate filaments. High levels of alkaline phosphatase activity are associated with regions of cellular interdigitation. The granuloma may serve to limit the spread of the parasite to surrounding tissues but does not appear to inhibit diffusion of oxygen and nutrients to the developing spores.

Sphaeromyxa zaharoni n. sp. (Myxosporea) is described from the gallbladder of devil firefish, Pterois miles (Scorpaenidae), from coral reefs of the Gulf of Eilat, Israel, northern Red Sea. The parasite was found also in bearded scorpionfish, Scorpaenopsis barbata, from the same area. This is the first report on Sphaeromyxa sp. from this zoogeographical region. The plasmodia are amoeboid when young, becoming disc-shaped and elongated when mature. In paraffin sections, the plasmodium periphery appears as a finely granulated, strongly eosinophilic layer with an intricate surface membrane network. Sphaeromyxa zaharoni n. sp. is polysporous, disporoblastic, and has asynchronous sporogenesis. The mature spore is elongated and fusiform, has delicately ridged valves, and contains a single, binucleated sporoplasm. In valvular view, the tips are truncated. The mean spore size is length 14.5 microm, width 4.8 microm, and polar capsule 4.8 x 3.4 microm. The 2 equally sized ovoid polar capsules are positioned at opposite ends of the spore, each containing a filament loosely folded in 2 loops. The fine structure of the sporoblast and spore corresponded with previously studied Sphaeromyxa species. According to small-subunit ribosomal DNA gene sequence analysis, S. zaharoni n. sp. is most closely related to 2 Myxidium spp. The close phylogenetic relatedness of Sphaeromyxa and Myxidium and similar spore morphology raises the question whether these 2 genera should be maintained in separate families and suborders.

Studies on Myxozoa have emphasized their potential impact on aquatic animal health but less on ecological aspects. In this investigation, we assess the importance of host and latitudinal variations in the morphometry of spores of Ceratomyxa Théohan, 1892 (Myxozoa) from the gall bladder of 3 ling Genypterus (Pisces; Ophidiidae) species. Discriminant analyses indicated that several morphospecies of Ceratomyxa coexist in these hosts, despite the fact that the specific level of taxonomic resolution of each spore was not attempted. At least 4 species, i.e., Ceratomyxa hokarari Meglitsch, 1960; Ceratomyxa inversa Meglitsch, 1960; Ceratomyxa laxa Meglitsch, 1960; and Ceratomyxa elongata Meglitsch, 1960 occur in the study area, and at least 2 species co-occur in each host and geographical location. The most widespread pattern found is that spores are larger in golden ling (Genypterus blacodes) and spore size decreases with increasing latitude; this may be associated with the species composition of these assemblages, as well as with the habitat and diet segregation of the host species.

Kudoa hypoepicardialis n. sp. infects the space between the epicardium and the compact myocardium and, in intense infections, the pericardial chamber of man-of-war fish (Nomeus gronovii) (Nomeidae) (the type host), blue runner (Caranx crysos) (Carangidae), Warsaw grouper (Epinephelus nigritus) (Serranidae), Atlantic tripletail (Lobotes surinamensis) (Lobotidae), northern red snapper (Lutjanus campechanus) (Lutjanidae), black drum (Pogonias cromis) (Sciaenidae), and bluefish (Pomatomus saltatrix) (Pomatomidae) in the northern Gulf of Mexico. This is the first report of a Kudoa sp. from the heart of a fish in the Gulf of Mexico, and of these hosts, only the bluefish was previously identified as a host for a species of Kudoa. Spores of the new species varied slightly in size among these hosts but were regarded as conspecific based on their nearly identical (99.9%) small-subunit (SSU) ribosomal DNA (rDNA) sequence. The new species differs both from the 4 nominal species of Kudoa reported from fishes in the Gulf of Mexico and from K. pericardialis, an allopatric species that infects the pericardial cavity, by the combination of having a large spore, a small polar capsule, and a polar filament with a single coil. The new species is morphologically and genetically most similar to K. shiomitsui, an allopatric species that infects the heart and pericardial cavity, but is distinguished from it based on a 4.2% difference in the SSU rDNA sequence. Heart lesions primarily were restricted to the vicinity of plasmodia and included a layer of fibrinous inflammation characterized by lymphocytes, macrophages, and granulomas as well as epithelioid encapsulations around plasmodia. Heavily infected hosts had melanin-like deposits and adipose cells beneath the epicardium. and the epicardium was discontinuous and apparently breached by plasmodia in some regions. Cardiac muscle, gill, liver, spleen, intestine, and kidney were normal.

The diagnosis of Kudoa funduli (Hahn, 1915) Meglitsch, 1948 (Myxozoa), is supplemented through study of new material collected from Fundulus heteroclitus (Cyprinodontidae) in coastal waters of Nova Scotia, Canada, and Connecticut. Plasmodia normally develop intracellularly in striated muscle of the flank and head, eventually rupturing and releasing spores. Spores disperse along adjacent epimysium, sometimes as far as the skin surface. Some plasmodia develop extracellularly within the bony cavities of vertebrae. Formalin-fixed spores viewed with a light microscope possess rounded edges, an inconspicuous apical region, thin sutural ridges, measure 6.6-7.4 microm wide, 4.3-5 microm thick, and 5.1-5.4 microm long, and have 4 equally sized polar capsules, 1.7-2.3 microm length by 1.4-1.7 microm width. Scanning electron microscopy revealed that spores are almost stellate, with inconspicuous uplifted tips, and that, within intracellular plasmodia, are embedded in an extensive honeycomb-like matrix. Prevalence of infection of K. funduli was 100% in host populations sampled in both Nova Scotia and Connecticut. Molecular sequence data of the 18S ribosomal DNA (737 base pairs) reveal that K. funduli is a valid species and a member of a clade that includes Kudoa dianae Dyková, Avila, and Fiala, 2002, Kudoa miniauriculata Whitaker, Kent, and Sakanari, 1996, and Kudoa paniformis Kabata and Whitaker, 1981.

Four new species of Ceratomyxa were found during parasitological studies of fish caught in shallow areas of Peter the Great Bay, Russia. Two of them (C. aspera n. sp. and C. durusa n. sp.) were found in the gall bladders of the flounders Limanda aspera and L. herzensteini. The third species (C. azonusi n. sp.) infected the gall bladder of the greenling Pleurogrammus azonus, and the fourth (C. lianoides n. sp.) was found in the gall bladder of Stichaeus grigorjewi. Ceratomyxa spp. have not been previously described from P. azonus or S. grigorjewi.

An intertidal horned blenny, Parablennius cornutus, captured at De Hoop Nature Reserve, South Africa, was found to harbor an unusual blood parasite and the haemogregarine Haemogregarina bigemina. In Giemsa-stained blood films, the enigmatic parasite occurred primarily as intraerythrocytic ringlike stages, with unstained centers and peripheral bands of beaded chromatin, not unlike Haemohormidium spp. Larger forms of the same organism stained pink with Giemsa, with nuclei occurring as 4-8 minute structures around the parasite body or distributed within it. These larger parasites apparently segmented into up to 8 individuals that were rounded or oval with deep-stained, comma-shaped or polar regions surrounding blue cytoplasm. Extracellular, binucleate, sporelike structures in clusters of as many as 16 individuals were also seen in blood films. Praniza larvae of the isopod Gnathia africana were seen in histological sections of gill tissue. Examination of spleen tissue by transmission electron microscopy showed intraerythrocytic organisms with ultrastructural characteristics like those of Haematractidium scombri, namely, a single boundary membrane, sometimes closely apposed nuclei with nucleoli, and profiles of dense material of variable structure. It is concluded that the parasite is probably related to Haemohormidium spp. and H. scombri, but it also shares features with some Microsporida.

To determine the potential for dissemination of myxozoan parasites by transfer of their alternate oligochaete hosts, shipments of tubificid worms obtained from an overseas commercial aquarium supplier were screened for actinospore stages of myxozoan parasites. At least 7 different triactinomyxon types were identified. The morphological characteristics of the actinospores recovered from these tubificids shared characteristics with triactinomyxons characterized in other surveys, particularly from eastern Europe. Analysis of the screened samples by polymerase chain reaction and comparison of morphological data indicated that these actinospores did not correspond to the triactinospore of Myxobolus cerebralis. Although identification of these triactinomyxon types was beyond the scope of this study, these data suggest that the unregulated import-export and exchange of live organisms for ornamental fish food may result in accidental introduction or dissemination of myxozoan parasites.

Development stages of a haemogregarine were found in Giemsa-stained heart blood smears of 3 of the 4 horned blennies (Parablennius cornmutus) captured at De Hoop Nature Reserve, South Africa. Gamonts of this haemogregarine conformed to an existing description of Desseria (Haemogregarina) fragilis from P. cornmutus, but intraerythrocytic trophozoites, as well as meronts undergoing division, were reported for the first time for this species. A detailed redescription of D. fragilis allowed its taxonomic re-evaluation. Intraerythrocytic division excluded D. fragilis from Desseria, whereas morphometric similarities and identical patterns of development lead to the conclusion that D. fragilis is the cosmopolitan haemogregarine, Haemogregarina bigemina. Nomenclatural correction synonymizing the 2 species is recommended.

Two unusual myxozoan parasites are described from the somatic muscle of 2 reef fishes from Australia's Great Barrier Reef. Kudoa quadricornis n. sp. from the somatic muscle of Carangoides fulvoguttatus is morphologically consistent with other Kudoa sp., having 4 polar capsules and 4 shell valves. Kudoa quadricornis n. sp. is unique in that it has a pyriform spore body with a greater length than width (7.82-9.95 and 5.94-8.66 microm, respectively) and distinct posterolateral projections. Spores of Kudoa permulticapsula n. sp. observed within pseudocysts of the somatic muscle tissue of Scomberomorus commerson are different from those of all other myxozoans. The ovoid spores (length, 4.69-6.65 microm; width, 8.42-9.92 microm; thickness, 6.36-8.33 microm) contain 13 polar capsules with an equal number of shell valves. Phylogenetic analysis using small subunit ribosomal DNA sequences of K. quadricornis n. sp. and K. permulticapsula n. sp. showed that these parasites cluster within a clade comprised of Kudoa species. This brings into question the division of parasites of the Multivalvulida into genera based solely on polar capsule numbers.

The marine polychaete Nereis (Hediste) diversicolor (Annelida) from shallow water in the Oresund, Denmark, was found to be infected with an actinosporean stage of a myxozoan parasite. The body length of the pyriform actinospore is 12-16 microm and its maximum width is 10-12 microm. The spore is triangular in apical view, with the 3 spherical polar capsules distally. The spore is without caudal processes. Eight spores develop in each pansporocyst. Free spores and pansporocysts were found in the musculature and parapodia but not in the intestine. The myxosporean stage in fish is unknown. This is the first record of an actinosporean stage in a marine polychaete, but because marine oligochaetes are rare, compared with polychaetes, the latter are believed to play an important role as invertebrate (alternate) hosts in marine myxozoan life cycles.

Proliferative kidney disease (PKD) of salmonid fishes is caused by the extrasporogonic stage of an enigmatic myxozoan, referred to as PKX. Sporogenesis occurs in the renal tubules, resulting in monosporous pseudoplasmodia. The spores are ovoid with indistinguishable valves and measure 12 microm in length and 7 microm in width. Two spherical polar capsules (2 microm diameter) with 4 coils occur at the anterior end of the spore. Prominent capsulogenic cell nuclei posterior to the polar capsules are evident in histological sections stained with hematoxylin and eosin. Regardless of the true nature of the valves (indistinguishable or absent), this myxozoan is morphologically distinct from all other described members of the phylum Myxozoa. Comparisons of small subunit rDNA sequences of PKX with other myxozoans demonstrated that it branches from all other members of the myxosporeans from fish examined thus far, including representatives of the phenotypically most closely related genera, Sphaerospora and Parvicapsula. Recent reports, based on rDNA comparisons, indicate that the alternate stage of PKX occurs in bryozoans, and that PKX clusters in a clade with Tetracapsula bryozoides. Our analyses and those of others, along with phenotypic observations, indicate that salmonids are the primary myxosporean hosts for PKX, that the cryptic spores of PKX in salmonids are the fully formed myxospores as they occur in the fish host, and that PKX represents distinct species that we previously place in the genus Tetracapsula in the family Saccosporidae. The latter 2 taxa were described based on stages from bryozoans, and the myxosporean stage in fish of the type species, T. bryozoides, has not been identified (if it exists). Thus, more complete resolution of the life cycle of both PKX and T. bryozoides, as well as more genetic data, are required to determine the precise relationship of these organisms.

Myxobolus petenensis n. sp. is described from the circumorbital integument of threadfin shad (Dorosoma petenense) in Kentucky Lake, Kentucky. Preserved spores are subspherical in frontal view and measure 10.1-13.1 microm long and 12.0-15.8 microm wide. The polar capsules are pyriform and often unequal in size, with the larger capsule measuring 6.6-8.0 microm long and 4.8-5.7 microm wide and the smaller capsule 5.7-7.4 microm long and 4.2-5.5 microm wide. Examination of several clupeids, skipjack herring (Alosa chrysochloris), gizzard shad (D. cepedianum), and threadfin shad revealed M. petenensis to infect only threadfin shad. This report of M. petenensis is the first known species of Myxobolus infecting a species of freshwater fish of the family Clupeidae in North America.

Six forms (5 of which are new) of echinactinomyxon and 5 new forms of the collective groups neoactinomyxum, aurantiactinomyxon, guyenotia, synactinomyxon, and antonactinomyxon of oligochaetes in Lake Sasajewun, Algonquin Park are described. Five forms of echinactinomyxon designated as echinactinomyxon 'A,' 'B,' 'C,' 'D,' and 'E,' a form of neoactinomyxum, and a form of aurantiactinomyxon were found in Limnodrilus hoffmeisteri. Echinactinomyxon radiatum, a form of synactinomyxon, and a form of antonactinomyxon were recorded from Tubifex tubifex. A form of guyenotia was found in Lumbriculus variegatus. The sporoplasmic mass of these actinosporeans was released through the anterior end of the epispore. An increase in the number of germ cells was observed in the floating spore stage of all forms except echinactinomyxon 'C' and the form of antonactinomyxon.

Eight forms of triactinomyxon and 6 forms of raabeia of oligochaetes from Lake Sasajewun, Algonquin Park are described. Of the 8 forms of triactinomyxon, 2 designated as triactinomyxon 'B' and 'E' were found in both Limnodrilus hoffmeisteri and Tubifex tubifex. Three additional forms, designated as triactinomyxon 'A,' 'C,' and 'D,' occurred in L. hoffmeisteri. One form infecting L. hoffmeisteri was identified as Triactinomyxon ignotum Stolc, 1899, and another infecting T. tubifex was tentatively identified as Triactinomyxon dubium Granata, 1924. One form infecting L. hoffmeisteri and Rhyacodrilus coccineus was designated as triactinomyxon 'F.' Of the 6 forms of raabeia, 4 designated as raabeia 'A,' 'B,' 'C,' and 'F' were found in L. hoffmeisteri, and 2 designated as raabeia 'D' and 'E' were recorded in T. tubifex. The sporoplasmic mass of each form of triactinomyxon usually moved posteriorly within the cavity of the spore axis and was released through its posterior end, whereas the sporoplasmic mass of each form of raabeia was released through the anterior end of the epispore. An increase in the number of germ cells was observed in the floating spore stage of triactinomyxon 'B,' 'D,' 'E,' and raabeia 'B.'

Three species of Myxobolus (Myxozoa, Myxosporea) occur in heart tissue of centrarchids. Myxobolus paralintoni Li and Desser, 1985 from Lepomis gibbosus in Algonquin Park and in Lake Erie, Ontario, has subcircular spores (in plane of spore length) in frontal view (11-13 microm long, 9-10 microm wide, and 5 microm thick) with a width-to-length ratio of 1:1.2. Myxobolus jollimorei n. sp. from Lepomis macrochirus in Lake Erie and in the Pascagoula River System, Mississippi, has subcircular spores (in plane of spore width) in frontal view (10.0-11.5 microm long, 12.0-14.5 microm wide, and 6.5-8.0 microm thick) with a width-to-length ratio of 1:0.8. Myxobolus manueli n. sp. from Pomoxis nigromaculatus in Lake Erie has spores (10-11 microm long, 8-10 microm wide, and 6.5-7.0 microm thick) that are nearly circular in frontal view but that have 2 distinct sublateral knobs along the sutural ridge and a width-to-length ratio of 1:1.2. All 3 species occur in the bulbus arteriosus of their hosts where they form small, saucer-shaped pseudocysts. Free spores were found free in the lumen of the heart and bulbus arteriosus, in bile, and in kidney tissue presses.

The actinosporean life stage of Ceratomyxa shasta, a myxozoan parasite of salmonids, and the annelid worm that serves as its alternate host were identified in laboratory transmission experiments and their roles were confirmed using molecular techniques. Infection by the parasite occurred in susceptible fish that were either exposed to or force fed the freshwater polychaete, Manayunkia speciosa, infected with the actinosporean. These observations were confirmed using the polymerase chain reaction with primers designed from the C. shasta 18S rDNA sequence. DNA was amplified from polychaetes harboring the actinosporean that caused infection in the fish but not from uninfected polychaetes. Amplified DNA from an infected polychaete was sequenced and its homology with the 18S rDNA sequence of C. shasta spores verified the proposed life cycle. Ultrastructural examination of the actinosporean in the polychaete showed developmental stages in the epidermis rather than within the intestinal epithelium as described for other myxozoans. The methods described will be useful in identifying alternate hosts and morphologically diverse life stages in the complex life cycles of other myxosporea and in understanding the relationships between these parasites and their hosts.

Myxobolus paralintoni Li and Desser, 1985, is redescribed from infected cardiac tissue of redbreast sunfish. Lepomis auritus Linnaeus, from the Potomac River in Montgomery County, Maryland. Mature and developing spores were contained within trophozoites from the collagenous connective tissues of the bulbus arteriosus. Two distinct trophozoites types were found; a thick-walled cyst and a relatively thin-walled "compartmentalized" cyst. Mature spores measure 11.7 13.5 microns in length and 9.0-10.6 microns in width. Polar capsule length and width are 4.5-6.5 microns and 2.7-3.8 microns, respectively, with no intercapsular process present. The sutural ridge had 8-11 triangular folds and the sporoplasm contained a large iodinophilous vacuole. Spores of M. paralintoni are compared with other morphologically similar species of Myxobolus reported from North America.

Myxobolus mississippiensis n. sp. is described from gill lamellae of the bluegill (Lepomis macrochirus) inhabiting the Pascagoula River System, Mississippi. Fresh spores measure 16.4-18.7 microns long, 3.9-6.2 microns wide, and 4.7-6.2 microns thick. Spore width to length ratio is 1:3.2. Polar capsules are 5.5-7.8 microns long and 1.5-2.3 microns wide, with 9-10 filament coils that when extruded measure 42.1 +/- 4.2 microns. This parasite is unique among known species of Myxobolus in having spores that are lenticular in frontal view.

The phylogenetic position of the phylum Haplosporidia was investigated with the complete small subunit rRNA gene sequences from 5 species in the phylum: Haplosporidium nelsoni and Haplosporidium costale, parasites of the eastern oyster Crassostrea virginica; Haplosporidium louisiana, a parasite of the mudcrab Panopeus herbstii; Minchinia teredinis, a parasite of shipworms (Teredo spp.) and Urosporidium crescens, a hyperparasite found in metacercariae of the trematode Megalophallus sp. in the blue crab, Callinectes sapidus. Multiple alignments of small subunit rRNA gene sequences included the 5 haplosporidian taxa and 14 taxa in the alveolate phyla Ciliophora, Dinoflagellida, and Apicomplexa. Maximum parsimony analysis placed the phylum Haplosporidia as a monophyletic group within the alveolate clade, as a taxon of equal rank with the other 3 alveolate phyla, and as a sister taxon to the clade composed of the phyla Dinoflagellida and Apicomplexa. Transversionally weighted parsimony placed the haplosporidians as a sister taxon to the ciliates. A separate analysis focused on the relationships of species in the genus Haplosporidium. Analyses were conducted with the haplosporidians as a functional ingroup, using each of the alveolate phyla individually as functional outgroups. The results indicated that species in the genus Haplosporidium do not form a monophyletic assemblage. As such, the present morphological criteria for distinguishing the genera Haplosporidium and Minchinia are insufficient.

Tetrauronema desaequalis n. sp. described from the bases of the ventral fins of the teleost Hoplias malabaricus Boch, 1794, was collected in an estuarine region of the Amazon river near Belem, Brazil. This myxosporean produces large cysts (1-2 mm in diameter) that represent plasmodia containing all life cycle stages, including spores. Spores averaged 22.5 microns in total length and possess 2 pairs of posterolateral unequal projections extending from beside the sutural ridges near the terminus of the shell valves. The spore body was ellipsoidal and laterally compressed. Spore bodies measured 13.6 microns in length, 6.5 microns in width, and 3.7 microns in thickness. The 4 projections averaged 13.0, 12.2, 7.2, and 5.1 microns in length. The ellipsoidal polar capsules (7.0 x 2.6 microns) possessed a polar filament with 9-11 turns.

A myxosporean producing aggregations of white pseudocysts in skin covering the posterior margin of the operculum and perioral tissue of Cottus cognatus in Lake Michigan is described as Myxobolus cognati n. sp. (Myxosporea). Histological sections revealed that the parasite develops in vascularized regions of the dermis and with development protrudes beyond the surrounding skin surface. Fixed spores are oval in front view, measure 12.0-14.0 microns long and 9.5-10.5 microns wide, and contain 8-11 filament coils wound tightly and perpendicular to the longitudinal axis of the capsule. Myxobolus cognati resembles Myxobolus rhinichthidis Fantham, Porter and Richardson, 1939 from subepithelial tissue of the operculum of the cyprinid Rhinichthys cataractae. Spores in the 2 species are the same size and shape. However, in contrast to those of M. cognati, spores of M. rhinichthidis have filament coils wound loosely at 45 degrees to the axis of the polar capsule and have no sutural ridge folds.

Samples of a marteiliad parasite in Mytilus galloprovincialis Lmk. from NW Spain were identified as Marteilia refringens, using light and electron microscopy. The most important lesions in the mussel tissues were found in the digestive tubules at the moment of the release of the sporangia, resulting in a breakage of the epithelial cells of the digestive tubules. The plasmodia of a Marteilia-like organism were also found in the gills, accompanied by a severe host reaction in 1 of the 4,200 examined mussels. The prevalence of the M. refringens parasite was monitored for 4 yr and correlation was found with prevalence, site, and depth of mussel culture. No correlation was found with geographical origin of the mussels. Mussels collected from the inner part of the Ría de Vigo were more frequently infected (38.5%) than those from the middle (29.0%) and outer parts (5.5%). Mussels from 2-m samples showed a higher mean prevalence of M. refringens than those from the 5-m samples (13.3 and 8.3%, respectively).

Kudoa intestinalis n. sp. (Myxosporea: Multivalvulida) is described from the intestinal musculature of the striped mullet, Mugil cephalus, from the southeastern coast of the Kii Peninsula, Japan. The plasmodia of the new species are spherical or ellipsoidal and contain quadrangular spores that, on the average, measure 3.4 microns in length, 6.5 microns in width and 6.1 microns in thickness. The species is characterized by the presence of short projections at the apex and concave values posteriorly.

Neospora caninum tissue cysts were found in the brain and spinal cord of a 1-wk-old lamb that was unable to stand after birth. The lamb was originally diagnosed as having toxoplasmosis, but ultrastructural and immunohistochemical techniques used in the present study permitted a definitive diagnosis of Neospora caninum tissue cysts in the brain and spinal cord of this lamb. This is the first report of N. caninum in sheep.

Experimental studies revealed that a freshwater ectoparasitic flagellate Ichthyobodo necator (Henneguy, 1883) could survive and reproduce in seawater after infected chum salmon fry, Oncorhynchus keta (Walbaum), were transferred directly from fresh water to 33% seawater. Minor morphological changes (slight reduction in body width, loss of twistlike wrinkles on body surface, and reduction in contractile vacuoles) were observed in the attached form of I. necator following transfer to seawater. The field survey also confirmed that I. necator occurs on chum salmon fry in seawater estuaries (salinity 17-34%) and in freshwater habitats. It was assumed that I. necator acquired salinity tolerance as a result of adapting to the migratory behavior of its anadromous host. Two morphologically similar bodonids, I. necator from chum salmon and Ichthyobodo sp. from marine Japanese flounder, Paralichthys olivaceus (Temminck and Schlegel), were differentiated by cross-infection experiments. Thus, the parasite from marine flounder should be regarded as a separate species from I. necator.

During May to August 1988, the prevalence of Lankesterella minima in bullfrog tadpoles and adults in the vicinity of Lake Sasajewun, Algonquin Park, Ontario, was 54.8% and 29.4%, respectively. The parasite was transmitted to laboratory-reared tadpoles through the bite of experimentally infected, laboratory-reared leeches (Batracobdella picta). Intraerythrocytic sporozoites were observed in the experimentally infected tadpoles 36 days postexposure (PE) to leech bites. Sporogonic stages in these tadpoles were examined by light and electron microscopy. Oocysts developed in vascular endothelial cells of several organs. Multinucleate oocysts at 29 days PE lay in a parasitophorous vacuole and contained several large inclusions. Mature oocysts, observed 32 days PE, contained about 70 sporozoites that exhibited typical apicomplexan features. In the posterior region of the sporozoites, 12 helically arranged chains of electron-lucent intrapellicular extended anteriorly from a dense terminal ring.

Unikaryon legeri (Dollfus, 1912) Canning and Nicholas, 1974, has been reexamined by electron microscopy from material collected in Portugal. It parasitises metacercariae of Meigymnophallus sp. in Cardium edule. A sporophorous vesicle forms around the sporonts, arising as a blister that separates from the electron-dense surface coat of the sporont. Sporogony is disporoblastic, giving rise to 2 spores that are retained in pairs within the sporophorous vesicle. Unikaryon piriformis, which is the type species of the genus and is also hyperparasitic in platyhelminth larvae, has not been examined by electron microscopy, and it is not known whether this species also produces sporophorous vesicles. If it does, then all that will be required is a simple addition of this character to the definition; if not, U. legeri will have to be transferred to a new genus and reclassified with other disporoblastic genera that sporulate in sporophorous vesicles.

We have shown that cysts of the genus Spironucleus share many common morphological features with Giardia cysts including: 2-4 nuclei, flagellar axonemes, a distinct cyst wall, and they even display the same immunostaining as Giardia cysts when labeled with antibodies specific for Giardia cyst wall. A direct comparison of Spironucleus muris and Giardia microti cysts have revealed that cysts of S. muris are significantly smaller than cysts of G. miroti. At the ultrastructural level, the cyst walls are similar in fibrillar appearance, but the width of the S. muris cyst wall is significantly less than that of G. microti. The cysts of S. muris also differ from G. microti in that they contain a striated rootlet fiber, flagellar sheath, and numerous glycogen rosettes. Characteristic features of Giardia include the adhesive disc and median body. Although the cysts of Spironucleus and Giardia are similar in appearance, these unique morphological features can be used to distinguish between the 2 protozoa and should be employed in the detection of Giardia cysts in water samples.

Ultrastructural aspects of interlamellar Henneguya exilis infections in channel catfish are reported. The plasmodium wall of this form differs from that of other species in that it is composed of two outer unit membranes which give rise to a zone of numerous pinocytic canals. Single-membraned canals appeared to be a stable feature of the wall while double-membraned canals are interpreted as those actively carrying out pinocytosis. Evidence suggests that host cellular cytoplasm as well as interstitial material is taken in by plasmodia. Plasmodium wall integrity, aggregation of parasite ectoplasmic components, numbers of pinocytic canals, and number of mitochondria proximal to the wall vary among different plasmodium profiles and may be related to plasmodium maturity. The parasite causes extensive hyperplasia of basal cells, which in turn replaces most other cell types found in noninfected gill filaments. Cytoarchitectural differences between basal cells of noninfected filaments and basal cells adjacent to plasmodia include significantly shorter microfilament bundles in the latter.

A new apicomplexan species, Perkinsus atlanticus, is described from gill filaments of the clam Ruditapes decussatus (Bivalvia) from Portugal, where it causes great mortality. The zoospores differ from those of other species of Perkinsus in size and shape, dimensions, insertion of the 2 flagella, and in the identity of the host. On the other hand, the life cycle stages showed some ultrastructural differences compared with Perkinsus marinus, the only species previously studied in detail. When the clams were parasitized heavily, ultrastructurally similar life cycle stages were found in foot and mantle tissues.

The flagella of several Trypanosomatidae (Trypanosoma cruzi, Herpetomonas samuelpessoai, Leptomonas samueli, Herpetomonas megaseliae, and Crithidia harmosa) were studied. Besides the axoneme, they have a filamentous, latticelike structure, the paraxial or paraflagellar rod. This structure was not observed in the flagellum of the intracellular spheromastigote form of Trypanosoma cruzi, but it appeared when the transformation of epimastigote and trypomastigote stages occured. Cross sections of the flagella show that the paraxial structure maintains a fixed position relative to the axonemal microtubules, being localized in a region comprised between doublets 4 and 7. Flagella of T. cruzi and H. samuelpessoai were isolated using the detergent lubrox PX. Most of them did not have a flagellar membrane. However, the paraxial structure remained associated with the axoneme. By negative staining, short projections were seen connecting the paraxial structure to the axonemal microtubules. The paraxial structure did not stain with phosphotungstic acid as occurs with the peripheral doublet microtubules, but it is formed by microfilaments longitudinally oriented in relation to the axoneme crossed in two directions by oblique filaments which make an angle of 45 degrees with the longitudinal ones.

Herpetomonas megaseliae grown in the presence of hydroxyurea showed a decline in population during the first 24 hr, eventually increasing slightly over the 7-day incubation. Throughtout the 7-day incubation period the population of the treated organisms never equaled that of the control organisms. The percentage of promastigotes, as opposed to para-and opisthomastigotes, in the treated cultures did not differ from that in the control cultures through the first 3 days in incubation. Thereafter, the percentage of promastigotes in the treated cultures dropped significantly below that of the controls. At the light microscope level, the treated organisms showed an increase in size with associated striations at the anterior end. A multiflagellate (nondividing) condition was also observed in the hydroxyurea-treated organisms. TEM and SEM studies showed pellicular convolutions, which were interpreted as the striations observed under the light microscope. The differnces in population number, kinetoplast number and position and pellicular morphology between control and experimental cultures suggests that enhanced differentiation and abortive cytokinesis are the net effects of hydroxyurea on Herpetomonas megaseliae.