Myxosoma funduli Kudo (Myxosporida) in Fundulus kansae: Ultrastructure of the Plasmodium Wall and of Sporogenesis*

SYNOPSIS Ultrastructure of the plasmodium wall and of sporogenesis were studied in Myxosoma funduli Kudo infecting the gills of Fundulus kansae (Garman). Plasmodia were located within the lamellar tissues adjacent to sinuses and capillaries. The plasmodium wall consisted of a single unit membrane which was continuous with numerous pinocytic canals extending into the parasite ectoplasm. The plasmodium membrane was covered by a surface coat of almost uniform thickness which prevented direct parasite-host cell contact. Numerous generative cells and cell aggregates, representing early stages of spore development, were seen in immature plasmodia. Later stages of spore development, including mature spores, were observed in older plasmodia. Sporogenesis was initiated by envelopment of one generative cell, the sporont, by a 2nd, nondividing cell, the envelope cell. The sporont and its progeny proceeded through a series of divisions until there were 10 cells, all compartmentalized within the envelope cell. Subsequently, the 10 cells became structurally differentiated and arranged into two 5-celled spore-producing units, each consisting of 1 binucleate sporoplasm and 2 capsulogenic cells, all surrounded by 2 valvogenic cells. Observations of later developmental stages revealed the major events of capsulogenesis, valvogenesis, and sporoplasm maturation, which occurred concomitantly during spore construction.     

Henneguya adiposa Minchew (Myxosporida) in the Channel Catfish: Ultrastructure of the Plasmodium Wall and Sporogenesis*

Wall ultrastructure and sporogenesis were studied in plasmodia of Henneguya adiposa Minchew which infects the channel catfish, Ictalurus punctatus (Rafinesque). Plasmodia were located among connective tissue bands of the adipose fin and were always separated from host fibrocytes by collagen fibers. The plasmodium wall consisted of a single unit membrane which was continuous with numerous pinocytic canals extending into the parasite's ectoplasm. The membrane was highly convoluted, producing an irregular parasite surface, and was covered by a fine granular coat of almost uniform thickness. Early sporogenic stages were located in a zone of cytoplasm rich in mitochondria, just interior to the zone of pinocytic canals. Later sporogenic stages, including mature spores, were concentrated in the center of the plasmodia. Sporogenesis began with the envelopment of one generative cell, the sporont, by a 2nd, nondividing, cell—the enveloping cell. The sporont and its progeny proceeded through a series of divisions until 10 cells were present within the enveloping cell. Once divisions were completed, the 10 cells became arranged into 2 identical spore-producing units, each consisting of one binucleate sporoplasm and 2 capsulogenic cells, all surrounded by 2 valvogenic cells. Later stages of spore development indicated that capsulogenesis, valvogenesis and sporoplasm maturation occurred concomitantly.     

Facieplatycauda pratti gen. n., sp. n. and Two New Species of Myxobolus (Myxosporida)*

Synopsis. Facieplatycauda pratti gen. n., sp. n. and Myxobolus kozloffi sp. n., from the Klamath Lake sucker, Catostomus luxatus (Cope), are described. The new genus is placed in the family Myxobolidae between Henneguya and Myxobolus. The spore valves beyond the sporoplasmic space are broad and long but not attenuated as an inverted triangle as in certain species of Myxobolus with tails, or of Henneguya with sometimes bifurcated tails. An organism resembling Myxobolus insidiosus (Wyatt & Pratt) was found in the muscle of the body of Salmo clarki (Richardson). Differences in spore structure and site of infection suggest this is a subspecies of the previous form which should be designated Myxobolus insidiosus clarki. A previously unreported species of Myxobolus from Cottus aleuticus (Gilbert) is also described.     

Ultrastructure of Red-Sore Lesions on Largemouth Bass (Micropterus salmoides): Association of the Ciliate Epistylis sp. and the Bacterium Aeromonas hydrophila*

SYNOPSIS. Epizootic outbreaks of red-sore disease in several reservoirs in the southeastern United States have been reported to cause heavy mortality among several species of fish having sport and commercial value. The etiologic agent is said to be the peritrich ciliate Epistylis sp.; secondary infection by the gram-negative bacterium Aeromonas hydrophila produces hemorrhagic septicemia which results in death. However, in recent studies on the largemouth bass Micropterus salmoides, Epistylis sp. could be isolated from only 35% of 114 lesions from 114 fish, while A. hydrophila was found in 96% of the same lesions. Transmission and scanning electron microscopy of lesions associated with red-sore disease indicate that neither the stalk nor the attachment structure of Epistylis sp. have organelles capable of producing lytic enzymes. Since other investigators have shown that A. hydrophila produces strong lytic toxins, and in absence of evidence to the contrary, it is concluded that Epistylis sp. is a benign ectocommensal and that A. hydrophila is the primary etiologic agent of red-sore disease.     

Ultrastructure and distribution of sensilla on the antennae of female fig wasp Eupristina sp. (Hymenoptera: Agaonidae)

In the species‐specific and obligate mutualism between the fig (Moraceae: Ficus spp.) and its pollinator (Hymenoptera: Agaonidae), the continuity of lifecycle of both partners completely depends on the female pollinator's ability to detect receptive figs. To better understand the chemical location mechanism, we examined the antennae and their sensilla of the female fig pollinator Eupristina sp. using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The antennae of female Eupristina sp. are geniculated, and in total, there were seven types of sensilla found on the antennae: two types of multiporous placoid sensilla (type 1 is sausage‐like and type 2 is rounded), sensilla trichodea (ST), basiconic sensilla (BS), chaetica sensilla (ChS), coeloconic sensilla (CoS), and one specialized sensillum classified as sensillum obscurum (SO). We described external morphology, abundance, distribution, ultrastructure and discussed putative functions. We inferred from their ultrastructures as chemoreceptors that two types of multiporous placoid sensilla, BS and CoS, were innervated by sensory neurons. The aporous type ST, ChS, and SO were not innervated by dendrites which may function as mechanoreceptor/proprioceptor. These results were also discussed in relation to the interaction between Eupristina sp. and its host fig.     

沙蒿大粒象触角感器的扫描电镜观察

应用扫描电镜技术,对沙蒿大粒象Adosomus sp.触角感器的类型、分布、数量以及雌雄之间的差异进行了详细研究。结果表明:沙蒿大粒象触角上共有5种感器类型,包括板形感器(Ⅰ、Ⅱ和Ⅲ型)、毛形感器和刺形感器。触角各节的感器类型和分布差异较大,以板形感器的分布最广、数量最多,在触角各节均有分布;刺形感器分布在索节第1亚节和棒节,而毛形感器仅分布在棒节且数量较少。雌雄触角的感器类型及分布基本一致,但分布数量上雄虫明显多于雌虫。     

Sphaeromyxa maiyai sp. n. (Protozoa: Myxosporidea), Coelozoic Parasite of the Pacific Tomcod,Microgadus proxiimus*

SYNOPSIS. Sphaeromyxa maiyai sp. n. (Myxosporidea: Myxiidae) is described from the gall bladder of the Pacific tomcod Microgadus proximus Girard, from Newport, Oregon. The plasmodial stage is discoid averaging between 1 and 2 cm. The spore averages 27.6 × 5.6 μm in breadth, with pyriform polar capsules measuring 9.3 × 3.7 μm. Scanning electron microscopy reveals the presence of numerous longitudinal striations.     

Ultrastructural studies of the hearts in Arenicola marina L. (Annelida: Polychaeta)

Summary The two hearts in Arenicola are capable of great dilation and contraction. The heart wall consists of myoepithelial cells resting on a basal lamina. On the luminal side of the basal lamina is a layer of collagen fibrils. No true endothelium was observed but occasional haemocytes were observed, subjacent to the collagenous layer. A few chloragogen cells are also found peripherally.The myofibrils are of a non-striated type consisting of thick and thin filaments and scattered Z-bodies. The sarcoplasmic reticulum forms a three-dimensional network. Only peripheral couplings were observed. The myofibrils are in contact with the sarcolemma on the luminal side of the cells, constituting a kind of hemidesmosome. The myoepithelial heart muscle is compared with other muscle types described in invertebrates. Supercontraction is discussed.     

纤毛虫念珠异列虫射出胞器的超微结构观察

应用扫描电镜术和透射电镜术显示,纤毛虫念珠异列虫(Anteholosticha monilata)的射出胞器早期发生在细胞质深处,附近有不同类型的囊泡结构。成熟后射出胞器向表膜迁移,结构由不同电子密度片层的体部、结晶状的中心轴杆部和多层膜的帽部组成。受外界刺激时胞器冲破皮层射出,形态呈"蘑菇"状。据上述观察结果推测:该射出胞器具有防御作用,它可能起源于高尔基体活动产生的小泡;在亲缘关系较近的纤毛虫中,其射出胞器可能具有相似的分化特征。     

A Scanning Electron Microscope Study on Gregarina sp. from Udeopsylla nigra*

Scanning electron microscope studies on Gregarina sp. from the cricket Udeopsylla nigra revealed that the epicytic folds of the younger gamonts are undulatory, whereas those of the older gamonts are relatively straight. The protomerite of the primite is conical with a mammiliform structure at the anterior tip, where the epicytic folds originate from a disc-like structure. The protomerite of the satellite is flattened.     

Myxobolus albi n. sp. (Myxozoa) from the Gills of the Common Goby Pomatoschistus microps Krøyer (Teleostei: Gobiidae)

ABSTRACT. A recent investigation into the myxozoan fauna of common gobies, Pomatoschistus microps , from the Forth Estuary in Scotland, revealed numerous myxosporean cysts within the gill cartilage. They were composed of polysporous plasmodia containing myxobolid spores that were morphologically different from the other known species of Myxobolus and from the myxosporeans previously recorded from this host (i.e. the ceratomyxid Ellipsomyxa gobii , infecting the gall bladder, and the kudoid Kudoa camarguensis , infecting the muscle tissues). Spores were ovoid, 9.4 × 9.1 μm with a thickness of 6.6 μm, with two pyriform polar capsules, the polar filaments of which had four to five turns. Molecular analysis of the parasite's small subunit rDNA region, based upon a contiguous sequence of 1,558 base pairs, discriminated it from other myxosporean species that have been characterized so far. A comparison of the spore morphology and the molecular sequences determined for this new isolate with other myxozoans described to date, confirmed its identity as a previously unknown myxobolid supporting the proposal that this isolate be elevated to the species level as a new species within the genus Myxobolus . A phylogenetic analysis places this new myxobolid, Myxobolus albi n. sp., in a basal position of a clade containing the majority of Henneguya spp. sequenced to date and various Myxobolus spp.     

Stempellia milleri sp. n. (Microsporida: Nosematidae) in the Mosquito Culex pipiens quinquefasciatus Say*

Stempellia milleri sp. n. was found in blood cells and the adipose tissue of field-collected larvae of Culex pipiens quinquefasciatus Say. Its development is different from other Stempellia species described in that it is dimorphic, producing two types of spores in adipose cells. Both were studied with the electron microscope. One spore is thin-walled and uninucleate; the other is thick-walled and binucleate. The latter spores are produced from sporonts that are somewhat similar to those of Nosema. Sporoblasts and spores of S. milleri were compared to those of Stempellia magna Kudo, and Stempellia lunata Hazard and Savage in both light and electron microscope preparations. S. milleri was transmitted experimentally to Culex pipiens pipiens, C. p. quinquefasciatus, C. salinarius, C. tarsalis, and C. territans. Transmission of S. magna to its host and other mosquito species was not possible. Although, generally low numbers of test larvae became infected with the pathogen, heavy infections were seen occasionally in individual specimens of its natural host, C. p. quinquefasciatus. Species of Aedes, Anopheles, Culiseta, Psorophora, and Uranotaenia exposed to spores of S. milleri were not susceptible to the disease.     

Observations on Haemogregarina balli sp. n. from the Common Snapping Turtle,Chelydra serpentina*

SYNOPSIS. Haemogregarina balli sp. n. is described from the blood and organs of the common snapping turtle Chelydra serpentina serpentina and from the gastric and intestinal ceca of the presumed invertebrate hosts, the leeches Placobdella parasitica and Placobdella ornata. In the peripheral blood of the turtle, male and female gametocytes and immature erythrocytic schizonts are found within erythrocytes. The maturation of erythrocytic schizonts containing 6–8 merozoites is recorded from liver imprints. Schizonts with 13–25 merozoites are found in various cells of the liver, lung and spleen. In the gastric ceca of the leeches the host erythrocytes are digested, releasing the gametocytes and immature erythrocytic schizonts. Immature erythrocytic schizonts degenerate. Association of the gametocytes occurs in the intestinal ceca. The microgametocyte apparently gives rise to 4 nonmotile microgametes, one of which fertilizes the macrogamete while the other remain as condensed, residual nuclei on the periphery of the developing oocyst. The oocyst increases in size with maturity. A mature oocyst produces 8 sporozoites from a single germinal center. Sporozoites liberated from the oocyst are found in the tissues of the leech. Transovarial transmission of the parasite does not occur in the turtle. Attempts at experimental transmission failed. Previously unfed (control) leeches were negative for the parasite. Haemogregarina balli is compared with other haemogregarines described from C. serpentina. Features of species of Haemogregarina and Hepatozoon as well as the taxonomy of these genera are discussed.     

Structure and development of stellate trichomes in Andradea ftoribunda Fr. Allem. (Nyctaginaceae)

LOURO, R. P., MIGUENS, F. C. & MACHADO, R. D., 1992. Structure and development of stellate trichomes in Andradea ftoribunda Fr. Allem. (Nyctaginaceae). Trichomes occur on both faces of young leaves. They are peltate-stellate on the abaxial face, and comprise a stalk and radiating cells with a rudimentary central apex. On the adaxial face the trichomes arc stellate with a large apex comprising one to three cells. In both cases the stalk is formed by three to six cells of which the most distal may contain a tannoid substance. In the adult leaf only the abaxial surface exhibits stellate trichomes, with two to three celled stalks. The central region of radial cells is depressed. On the adaxial side the hairs are shed during maturation of the leaf.     

Structure, Cytochemistry, and Locomotion of Haemogregarina sp. from Rana berlandieri

Intra- and extracellular gametocytes of Haemogregarina sp. from Rana berlandieri were studied by light and electron microscopy. Locomotion in free gametocytes appears to be related to series of horizontal “peristaltic” waves of constriction, passing from anterior to posterior along the body. Intracellular gametocytes lie within a vacuole in the erythrocyte cytoplasm. The pellicle of the parasite consists of a trilaminar plasmalemma and an inner electron dense layer, beneath which lies a ring of 80 microtubules. The inner dense layer becomes thickened and modified in the apical region, to form a cap-like structure. The gametocytes contain a prominent nucleus, several mitochondria, and many granular inclusions. One type of inclusion consists of elliptical, electron-dense, profeinaceous bodies scattered throughout the cytoplasm, while other inclusions are larger and electron-opaque, polysaccharide in nature, and occur predominantly in the pre- and post-nuclear regions. In the electron microscope, pronounced pellicular folds were observed in longitudinally sectioned extracellular gametocytes. These folds are thought to represent the waves of constriction seen in motile specimens by light microscopy. The mechanism of movement of the parasite is discussed and compared with that in haemosporidian ookinetes, as well as in gregarines.     

Haemogregarina pseudemydis n. sp. (Apicomplexa: Haemogregarinidae) and Pirhemocyton chelonarum n. sp. in Turtles from Louisiana*

SYNOPSIS. The blood of each of 95 turtles (8 species) collected from southeastern Louisiana was infected with some or all of the merogonic stages and gametocyte stage of Haemogregarina pseudemydis n. sp. Five species of turtles harbored Pirhemocyton chelonarum n. sp. Turtle Haemogregarina and Pirhemocyton are locality records for Louisiana. Pirhemocyton is reported for the first time in turtles and in the continental U.S.A.     

Diplodinium (Ostracodinium) minorum sp. n., Ciliate from the Rumen of Domestic Sheep*

SYNOPSIS. Diplodinium (Ostracodinium) minorum sp. n., observed in rumen contents from several domestic sheep, resembles Diplodinium (O.) ypsilon and Diplodinium (O.) magnum. It differs from the latter 2 species primarily in the size and proportions of the body, size of the rectum and anus, and in the presence of a short right caudal lobe in many individuals. In the samples studied, D. (O.) minorum constituted from 0.06 to 0.67% of the total rumen ciliate population.     

Merlinius paniculoides n. sp. from Italy (Tylenchina: Belonolaimidae)

Merlinius paniculoides n. sp. is described from a bisexual Italian population found in northern Italy. This species has a coarsely annulated cuticle with approximately 30 longitudinal striae in addition to the six lateral field incisures; consequently the cuticle appears tessellate. The female tail is subcylindrical with a bluntly, rounded, non-annulated terminus. Merlinius paniculoides shares the tessellate cuticular ornamentation and the offset labial region with M. lenorus (Brown, 1956) Siddiqi, 1970 and M. tartuensis (Krall, 1959) Siddiqi, 1970. It differs from M. lenorus by the higher c and lower c'' ratios (c = 16-19 vs. 12-15 and c'' = 2.2-2,8 vs. 3.7) and greater number of longitudinal striae (28-32 vs. 24). It differs from M. tartuensis by a fewer number of annuti from stylet knob base to lip constriction (8-9 vs. 21), shorter stylet (19-21 vs. 24 μm), presence of males, and higher c'' value (c'' = 2.2-2.8 vs. 1.9).     

Histological studies on the host response to Myxobolus artus Akhmerov, 1960 (Myxozoa: Myxobolidae) infection in the skeletal muscle of carp, Cyprinus carpio L.

Myxobolus artus infection of carp is reported for the first time from Japan. In most cases, it took the form of interfibrillar pseudocysts in the skeletal muscle, some showing abnormal growth, imperfect encapsulation of the parasite by the host connective tissue and irregular development of the ectoplasm. Such atypical pseudocysts probably ruptured before the completion of sporogenesis, causing lysis of adjacent muscle fibres. Intrafibrillar pseudocysts were also present. After spore formation was complete or atypical pseudocytes were ruptured host reaction was initiated. Spores were phagocytosed and transported to the melanomacrophage centres in the kidney, liver, spleen etc. Phagocytosed spores were also observed in the capillaries and epithelial tissues of various organs, suggesting that the spores were transported there from the skeletal muscle through the host vascular system. They are thought to be discharged from the host through the skin and intestine.