Fine structure of trophozoites of the gregarine Leidyana ephestiae (Apicomplexa: Eugregarinida) parasitic in Ephestia kuehniella larvae (Lepidoptera)

The ultrastructure of the eugregarine Leidyana ephestiae, parasitic in the larval gut of the flour moth, Ephestia kuehniella, is described. Guts of experimentally infected larvae of E. kuehniella were fixed and sectioned for electron microscope studies of young and mature trophozoites. Young unsegmented trophozoites were small, oval to ovoid, and possessed a simple, globular epimerite. The plasma membrane covering the epimerite region was continuous with the plasma membrane of the protodeutomerite and was in close contact with that of the host cell. Three cortical membranes covered the protodeutomerite region. Folding of the protodeutomeritic epicyte occurred after about 2 days of development of the gregarine. After 3–4 days the body of the trophozoite became differentiated into three segments. A septum was visible between protomerite and deutomerite, but there was nothing similar to this structure between epimerite and protomerite. Fully developed trophozoites showed a large ovoid epimerite containing many mitochondria and vesicles. The epimerite was situated on a short neck filled with fibrils. The cytoplasm of protomerite and deutomerite was rich in amylopectin granules and electron-dense bodies.     

Cytology of Leidyana canadensis (apicomplexa: eugregarinida) in Lambdina fiscellaria fiscellaria larvae (lepidoptera: geometridae)

The eugregarine Leidyana canadensis infects the larval gut of the eastern hemlock looper, Lambdina fiscellaria fiscellaria. Guts of infected larvae were chemically fixed, embedded in epoxy resin, and sectioned for light and electron microscopy to describe the cytology of L. canadensis and its pathology in the larval host. Oocysts of L. canadensis are ingested by larval hemlock looper. Trophozoites emerge from the oocysts, pass through the peritrophic membrane into the ectoperitrophic space, and attach to the epithelium of the midgut by means of an apical epimerite. The epimerite does not actually penetrate the affected epithelial cell; instead, it causes an invagination of the plasma membrane of the cell. The center of the epimerite contains membrane cisternae, and mitochondria line its periphery. Microtubules and mitochondria in the host cell cytoplasm surround the epimerite. At the light microscopic level, there appeared to be septa between the epimerite and the protomerite and between the protomerite and the deutomerite; however, in the electron microscope, no septa were evident. Only differences in the concentrations and nature of the inclusions in the cytoplasms of these three regions were apparent. The deutomerite contains a single nucleus in the central-posterior area. After an undetermined period, the epimerite detaches from the host gut epithelium and is withdrawn into the protomerite, and the trophozoites float freely in the ectoperitrophic space before differentiating into gamonts. Division of the single, large nucleus into numerous small nuclei appears to occur prior to syzygy. Gamonts pair and a cyst wall is laid down around them, forming a gametocyst. Oocysts are extruded from mature gametocysts, in chains, through sporoducts.     

Chronology of the ultrastructural modifications during the growth of Gregarina blaberae]

In an ultrastructural study the development of the sporozoite as well as the growth and development of the trophozoite of Gregarina blaberae were followed in the course of experimental infections of larvae of the cokroach Blaberus craniifer. The spectacular growth involved the transformation within 18 days of the sporozoite, measuring 15 X 1 micronm, to a cephaline--trophozoite affixed to the intestinal epithelium--of 250 micronm length and 65 micronm diameter. The sporozoite's ultrastructure is not different from that of sporozoites of other Sporozoa studies to date--the conoid and dense bodies are present. The pellicle consists of 3 membranes, but there are some interruptions in the internal membrane complex. The first dictyosomes are formed from the nuclear envelope. The migration of the nucleus and of the dense bodies, followed by the regression of all the structures characteristic of the sporozoites, and the establishment of a cortical zone that comes to cover the epimerite, take place within 48 h after infection and mark the transformation of the sporozoite into the trophozoite. Development of the cephaline involves the formation of the epicytic folds, which occurs at the base of the deutomerite, starting on the 3rd day of development. A regular system of longitudinal or epicytic folds is formed over the entire surface of the gregarine. On the 4th and 5th days of development, a vacuolar system and a chondriome become differentiated in the epimerite, while a fibrillar septum separates the protomerite from the deutomerite. The next stage, starting on the 6th day, is characterized by distribution of polysaccharide reserves between these 2 segments. The model studied allows us to determine the role of the epimerite in the parasite's nutrition, as well as the development of the chondriome and of the cortical membranes in the course of the vegetative growth phase of the cephaline gregarine.     

Chronologie des Modifications Ultrastructurales au Cours de la Croissance de Gregarina blaberae*

SYNOPSIS. In an ultrastructural study the development of the sporozoite as well as the growth and development of the trophozoite of Gregarina blaberae were followed in the course of experimental infections of larvae of the cockroach Blaberus craniifer. The spectacular growth involved the transformation within 18 days of the sporozoite, measuring 15 × 1 μm, to a cephaline—trophozoite affixed to the intestinal epithelium—of 250 μm length and 65 μm diameter. The sporozoite's ultrastructure is not different from that of sporozoites of other Sporozoa studied to date—the conoid and dense bodies are present. The pellicle consists of 3 membranes, but there are some interruptions in the internal membrane complex. The first dictyosomes are formed from the nuclear envelope. The migration of the nucleus and of the dense bodies, followed by the regression of all the structures characteristic of the sporozoites, and the establishment of a cortical zone that comes to cover the epimerite, take place within 48 hr after infection and mark the transformation of the sporozoite into the trophozoite. Development of the cephaline involves the formation of the epicytic folds, which occurs at the base of the deutomerite, starting on the 3rd day of development. A regular system of longitudinal or epicytic folds is formed over the entire surface of the gregarine. On the 4th and 5th days of development, a vacuolar system and a chondriome become differentiated in the epimerite, while a fibrillar septum separates the protomerite from the deutomerite. The next stage, starting on the 6th day, is characterized by distribution of polysaccharide reserves between these 2 segments. The model studied allows us to determine the role of the epimerite in the parasite's nutrition, as well as the development of the chondriome and of the cortical membranes in the course of the vegetative growth phase of the cephaline gregarine.     

Gregarina coronata N. Sp. (Apicomplexa: Eugregarinida) Described from Adults of the Southern Corn Rootworm, Diabrotica undecimpunctata howardi (Coleoptera: Chrysomelidae)

ABSTRACT. Gregarina coronata n. sp. (Apicomplexa: Eugregarinida) is described from the adults of the Southern Corn Root Worm, Diabrotica undecimpunctata howardi (Coleoptera: Chrysomelidae). Measurements given are means, in micrometers, taken from mature gamonts in association. Primite: protomerite hemi-ellipsoidal with basal tumidus, length 47.6, width 44.0, with cytoplasmic granule, apical crown apparent; deutomerite elongate ellipsoidal, length 227.9, width 81.3; epimerite absorbed into anterior in gamont, globular in trophozoite. Satellite: protomerite hemi-ellipsoidal, truncated at association interface to appear trapezoidal, length 39.2, width 49.6, with cytoplasmic granule; deutomerite elongate ellipsoidal, length 240.6, width 80.2; epimerite absorbed into anterior in gamont. Association caudofrontal and often precocious, occurring during growth of trophozoites. Gametocysts spherical, 115.3 in diameter, 132.9 with hyaline coat; producing multiple oocyst chains under moist storage in 24–36 h. Oocysts very uniform in shape and size, dorsad: doliform, length 6.4, equatorial width 3.4, polar width 2.9; pleuron: dorso-ventrally flattened, corpus concave with bicondylic termina; corpus height 0.98, width 4.44; terminus height 1.96, width 0.98.     

Naiadocystis phykoterion n. gen., n. sp. (Apicomplexa: Eugregarinida: Hirmocystidae), from the Mexican pygmy grasshopper, Paratettix mexicanus (Orthoptera: Tetrigidae), in the Texas big thicket with recognition of three previously described species of Naiadocystis

Naiadocystis phykoterion n. gen., n. sp. (Apicomplexa: Eugregarinida: Hirmocystidae), is described from the Mexican pygmy grasshopper, Paratettix mexicanus (Orthoptera: Tetrigidae), collected from sandbars along Harmon Creek, Walker County, Texas, in the western edge of the Texas Big Thicket. Naiadocystis n. gen. is distinguished by the form of the epimerite complex, a simple cordoid or toroid epimerite with an interior obconoid structure resembling a funnel that tapers to a distinct axial canal bisecting the protomerite, which is conspicuous in all stages of development, and a satellite protomerite reduced to a linearly crateriform cup or sucker that receives and enfolds posterior end of primite deutomerite. Association is precocious, caudofrontal, and biassociative. Gametocysts are spherical. Sporoducts are present but vestigial and irregular in number. Oocysts are broadly elliptoid with 4 small spherical polar knobs, 1 each at 30 degrees, 150 degrees, 210 degrees, and 330 degrees, and dehisce en masse. The species described herein are differentiated by their overall size and relative proportion of cellular structures. Naiadocystis acantholobae (Hoshide, 1952) n. comb., Naiadocystis acrydiinarum (Semans, 1939) n. comb., and Naiadocystis tetrigis (Corbel, 1968) n. comb. are recognized as members of Naiadocystis previously placed within Gregarina (Apicomplexa: Eugregarinida: Gregarinidae).     

Morphological analysis of the cellular interactions between the eugregarine Gregarina garnhami (Apicomplexa) and the epithelium of its host, the desert locust Schistocerca gregaria

Morphological features of the eugregarine Gregarina garnhami (Canning, 1956) parasitic in the caeca and mid-gut of the desert locust, Schistocerca gregaria, have been studied by transmission and scanning electron microscopy, with particular attention to the epimerite and the relationship between the epimerite and the host epithelium. The cytoplasmic core of the globular epimerite is overlain by a distinct cortical zone, limited on its cytoplasmic face by a membrane-like structure, with an underlying layer of mitochondria. The periphery of the cortical zone is strengthened by a mass of fine filaments, especially at its base. Fine tubular structures, apparently arising from the membrane-like structure, pass through the cortical zone and attach to the epimerite-host cell interface. The base of the cortical zone is supported by a distinct osmiophilic ring. The epimerite is separated from the rest of the gregarine body by a discontinuous septum. Maturing and mature trophozoites possess conically arranged fibrils, which arise from the epimeritic septum and continue into the protomerite region. The epimerite and associated structures are here discussed with regard to the detachment of the trophozoite from the host epithelium. In individuals already detached from the host epithelium, a central depression remained at the top of their protomerite, in the area formerly bearing the epimerite.     

Eugregarine trophozoite detachment from the host epithelium via epimerite retraction: Fiction or fact?

Eugregarines represent a diverse group of Apicomplexa parasitising numerous invertebrates. Their sporozoites generally develop into epicellular trophozoites attached to the host epithelium by a specialised attachment organelle known as an epimerite. They are considered peculiar protists due to their unique cell architecture and dimensions as well as their attachment strategy which is similar to that of cryptosporidia. Using electron and fluorescence microscopy, the fine structure of the epimerite with associated structures and the mechanism of trophozoite detachment from the host epithelium were studied in Gregarina polymorpha parasitising the intestine of Tenebrio molitor larvae. The epimerite appears to be a very dynamic structure whose shape dramatically changes depending on whether or not it is embedded into the host epithelium. The trophozoite’s most fragile zone is the area below the membrane fusion site at the epimerite base. The epimerite plasma membrane forms basal radial ribs which are involved in increasing its surface and strengthening the epimerite-host cell junction. FITC-phalloidin labelling demonstrated the presence of filamentous actin in trophozoites along with its accumulation at the epimerite base and in the apical end of the protomerite, as well as a patch accumulation of filamentous actin in the protomerite of maturing and mature trophozoites. Indirect immunofluorescence revealed the presence of myosin in the cortical zone of the epimerite and in the membrane fusion site area. The data obtained strongly suggest that these structures could facilitate the detachment of a mature trophozoite from the host epithelium. Supported by data presented herein and our previous observations, we propose a new hypothesis on the mechanism of trophozoite detachment from the host epithelium based on epimerite retraction into the protomerite. This is contrary to the commonly accepted hypothesis describing gradual epimerite constriction and subsequent separation facilitated by contractility of the membrane fusion site (osmiophilic ring).     

Two New Menosporine Gregarines, Hoplorhynchus acanthatholius N. Sp. and Steganorhynchus dunwoodyi N. G., N. Sp. (Apicomplexa: Eugregarinorida: Actinocephalidae) from Coenagrionid Damselflies (Odonata: Zygoptera)

ABSTRACT. Hoplorhynchus acanthatholius , n. sp. is described from Enallagma civile , the Civil Bluet damselfly. Trophozoites are solitary, lie in the mesenteron between the peritrophic membrane and the epithelium, and attain a maximum length of 850 μm. Epimerite ovoid to broadly ovoid; anterior margin bearing eight equidistant retroarcuate hooks; attached to protomerite by means of a vermicular stalk. Protomerite ovoid; deutomerite narrowly obvoid. Gametocysts spherical; diam 300 μm, sporulating by simple dehiscence in 48–72 h. Oocysts are characteristic of Menosporinae: smooth, biconical, crcscentic, uniform in size and shape. Steganorhynchus dunwoodyi , n. g., n. sp. is described from the damselfly Ischnura verticalis. The genus is characterized by an epimerite comprising an ovoid papilla enclosed in a retractable, globular sheath, borne on a long vermicular stalk. Trophozoites are solitary, lie in the mesenteron between the peritrophic membrane and epithelium, and attain a maximum length of 605 μm. Protomerite very broadly ovoid; deutomerite obvoid. Gametocysts spherical; diam 258 μm, sporulating by simple dehiscence in 48–72 h. Oocysts are characteristic of Menosporinae: smooth, biconical, crescentic, uniform in size and shape. The population dynamics of H. acanthatholius and S. dunwoodyi among damselfly populations in five Nebraska localities are presented.     

Clitellocephalus americanus n. gen., n. sp. (Apicomplexa: Eugregarinida: Gregarinidae) from Cratacanthus dubius (Coleoptera: Carabidae: Harpalinae) in the Nebraska sandhills and Clitellocephalus ophoni n. comb. (Apicomplexa: Eugregarinida: Gregarinidae) from Ophonus pubescens (Coleoptera: Carabidae: Harpalinae) in Sète,France

Clitellocephalus americanus n. gen., n. sp. (Apicomplexa: Eugregarinida: Gregarinidae) is described from Cratacanthus dubius (Coleoptera: Carabidae) collected from Keith County in the Sandhills of western Nebraska. Clitellocephalus ophoni n. comb. is redescribed using original type material from Ophonus pubescens (Coleoptera: Carabidae) collected in Sète, France. Clitellocephalus n. gen. is distinguished by a deltoid epimerite with an internal anterior obconoid structure and a basal toroidal vacuole, which is retained in gamonts. Protomerites are broadly elliptical to cylindrical; deutomerites are narrowly obovate. Association is precocious, caudofrontal, and biassociative, with the satellite protomerite engulfing the posterior end of the primite deutomerite to form an interlock. Gametocysts are spherical. Sporoducts are present but reduced and irregular in number. Oocysts are dolioform, dehiscing in chains. The species described herein are differentiated by their overall size and relative proportion of cellular structures.     

The life cycle of Gregarina ronderosi n. sp. (Apicomplexa: Gregarinidae) in the Argentine grasshopper Dichroplus elongatus (Orthoptera: Acrididae)

Gregarina ronderosi n. sp. is described based on life cycle observations conducted on nymphs and adults of its natural host, the grasshopper Dichroplus elongatus. Following ingestion of oocysts by the host, parasite development occurs between the epithelium and the food mass in the midgut and gastric caeca. Gametocysts are liberated in the faeces. Natural prevalence in the type locality, Girondo, northwestern Buenos Aires Province, was 39.7% (n=131). The earliest trophozoites seen were small (< or = 10 microm), somewhat ovoid, unsegmented bodies. Fully developed trophozoites (the body is divided into epimerite, protomerite, and deutomerite) were slender, with conical or globular epimerites in attached or unattached forms, respectively. Trophozoites varied greatly in size [total length: 10.4-275.1 microm; mean (+/-S.E.): 126.3+/-78.9]. Gamonts, which were the most common stages observed and filled the midgut and gastric caeca in grasshoppers kept in rearing rooms, had a stocky appearance and also varied greatly in size (total length: 80-348 microm; 205+/-13). Association of gamonts was precocious, biassociative, and caudofrontal. Gametocysts were spherical and highly variable in size (96-376 microm in diameter; 202.8+/-52.5), and normally have 14 sporoduct basal discs. Everted sporoducts were up to 60 microm long. Oocysts were uniformly doliform in shape, measured (5+/-0.08 by 3.2+/-0.06 microm) and contained eight sporozoites. Wall reinforcements (carinae) were present. No infection resulted in experimentally inoculated Locusta migratoria, which is a host of Gregarina acridiorum. G. ronderosi is strikingly similar to G. acridiorum, but has larger oocysts.     

Epimerite-host epithelium relationships among eugregarines parasitizing the damselflies Enallagma civile and Ischnura verticalis.

The host-parasite interface between 2 species of damselflies and 4 species of eugregarines was examined at the ultrastructural level. Nubenocephalus nebraskensis organisms attached to the host midgut epithelium by means of a sucker-like protomerite; the space between the epicytic folds and host epithelium was filled with electron-dense material interpreted to be adhesive in nature. Actinocephalus carrilynnae organisms attached by means of the epimerite, which had no epicytic folds, and by the fluted stalk with characteristic epicytic folds: host cell and parasite membranes appeared fused at some places on the epimerite. Hoplorhynchus acanthatholius organisms attached by means of an ovoid epimerite with backward-pointing digitations; the entire epimerite was embedded in a host cell, and host cell microvilli surrounded the stalk. Steganorhynchus dunwoodyi organisms attached by means of an ovoid stalk papilla enclosed in a retractable globular sheath; the papilla was covered with epicytic folds, but the sheath was not, and the sheath had a single membrane, whereas the epicytic folds had 2 or 3 membranes. The entire apparatus was inserted between epithelial cells, and the sheath was highly folded at its surface. The ultrastructural observations suggest that actinocephalid gregarines have evolved 2 general strategies for attaching to the host epithelium, that is, suckerlike protomerites, as in the case of N. nebraskensis, and deeply embedded epimerites inserted within or between host cells, as in the other species studied.     

Leidyana phryganidiae and Leidyana berkeleyi: Two new species of gregarines from Phryganidia californica

Larvae of the California oakworm, Phryganidia californica, collected in August 1958 in Orcutt, California, were infected by two eugregarines, Leidyana phryganidiae n. sp. and L. berkeleyi n. sp. Both gregarines inhabit the intestine of larvae, and their sporonts are solitary. The maximum length of sporonts of L. phryganidiae is 633 μm; the ratio of length of protomerite to total length (LP:TL) ranges between 1:6.6 and 1:9.6, and the ratio of width of protomerite to width of deutomerite (WP:WD) ranges between 1:1.3 and 1:2.2. The protomerite is conical, longer than wide, and the deutomerite tapers sharply to a point. The maximum length of sporonts of L. berkeleyi is 422 μm; the ratio LP:TL ranges between 1:4.6 and 1:11.2 and WP:WD between 1:0.9 and 1:2.1. The protomerite is hemispherical, and the deutomerite is cylindrical. This is the first record of eugregarine infection in a phytophagous lepidopteran.     

Leidyana canadensis N. Sp. (Apicomplexa: Eugregarinida) from Larval Eastern Hemlock Looper, Lambdina fiscellaria fiscellaria (Lepidoptera: Geometridae)

ABSTRACT. Leidyana canadensis n. sp. (Apicomplexa: Eugregarinida) is described from larvae of the eastern hemlock looper, Lambdina fiscellaria (Lepidoptera: Geometridae) collected near St. Stephen, Charlotte County, New Brunswick, Canada. Gamonts solitary, located between host ventricular peritrophic membrane and ventricular epithelium. Protomerite very broadly ellipsoid with transverse posterior margin; length 43.7 μm, width 42.7 μm; protomerite-deutomerite septum strongly constricted. Deutomerite narrowly obovoid with anterior transverse margin; length 186.6 μm, width 58.7 μm; total length 227.1 μm. Nucleus spherical to broadly ellipsoid; length 26.3 μm, width 20.2 μm; placement abaxial in the posterior 2/3 of the deutomerite. Nucleus often obscured in late gamonts. Association late, caudofrontal, ephemeral and leading directly to syzygy. Gametocysts roughly spherical; diameter 216.7 μm; hyaline coat increasing diameter to 359.1 μm. Gametocysts mature and dehisce through six short spore tubes within 48 hours. Oocysts axially symmetric, dolioform in dorsal aspect, compressed in the plane perpendicular to the major axis, very uniform in size and shape; length along major axis 5.2 μm, terminal width 1.8 μm, medial width 3.8 μm; extruded in chains.     

Myosin-Like Protein (MR 175,000) In Gregarina Blaberae

ABSTRACT. A myosin-like protein (M_r 175,000) was detected in the parasitic protozoan Gregarina blaberae , by both immunofluorescence and immunoblotting of one- and two-dimensional electrophoresis gels using anti-myosin antibodies. This protein was present in the trophozoite ghost but not in the cytoplasmic extract, nor in extract from the sexual stage, suggesting a protein-stage-dependent expression. the protein tightly bound to the cortical membranes was insoluble at low ionic strength, or in detergent solutions, but could be extracted from Gregarina ghosts by 6 M urea in high ionic strength solution (0.5 M NaCI) and in the presence of reducing agents (20 mM DTT). the protein was localized by indirect immunofluorescence in the cortex of the epimerite, in the fibrillar disc (the socalled septum) separating the proto- and the deutomerite segments, in the contractile ring or sphincter at the top of the protomerite, and as longitudinal lines underlying the G. blaberae epicyte folds. the presence of both actin-like and myosin-like proteins would be consistent with a role in gliding and other cell motility processes of this parasite.     

Stylocephalus occidentalis n. sp. (Apicomplexa: Eugregarinida: Stylocephalidae) from Trimytis pruinosa (Coleoptera: Tenebrionidae) in the Nebraska Sandhills

Stylocephalus occidentalis n. sp. (Apicomplexa: Eugregarinida) is described from Trimytis pruinosa (Coleoptera: Tenebrionidae) collected from Keith County in the Sandhills of western Nebraska. Measurements are means in micrometers. Developing trophozoites solitary; epimerite a complex of terminal epimerite and intercalating diamerite; epimerite shallowly ovoid to transversely elliptoid, with transverse basal constriction at junction with diamerite, length 0.5-1 times width, approximately 3-4 times that of diamerite; width approximately equal to that of diamerite; diamerite roughly cylindrical to spindle-shaped, without significant anterior taper, little or no evidence of longitudinal folds, length approximately twice width. Association late, frontal, isogamontic. Gamont protomerite depressed ovoid to very broadly ovoid, length 27.3, width 35.1, anterior distance to widest point 15.4. Protomerite-deutomerite septum clearly marked and constricted, width 34.6. Deutomerite often with distinct marginal crenulation, narrowly obovoid to very narrowly obovoid, length 356.5, maximum width 57.6, anterior distance to widest point 26.3, equatorial width 35.1, +/-12.5, 29. Total length 381.5. Nucleus ellipsoid, length 32.5, width 18.8; with 0 or 2 polysomal endosomes. Gametocysts roughly spherical; diameter 205.0; wall desiccating to become paper-like, slightly papillated, dehiscing by simple rupture, releasing oocysts in coiled chains, epispore packet absent, gametocyst residuum present. Oocysts dark brown to black, axially asymmetric, broadly deltoid, gibbous in lateral aspect, slightly keeled in dorsal aspect; length 9.8, height 7.9; with slight terminal protuberances and 2 central, spherical residua.     

Ultrastructure of Sporozoites and Zoites of Hammondia heydorni

The ultrastructure of sporozoites and zoites of Hammondia heydorni was studied in cultured bovine cells. In addition to ultrastructural features typical of coccidian parasites, H. heydorni sporozoites and zoites contain rhoptries that are located posteriorly as well as anteriorly. Also, sporozoites contain a posteriorly located crystalloid body (1.2 μm in diameter); a small crystalloid body (0.5 μm in diameter) was occasionally seen in the anterior end. Zoites resulting from the 1st division of endodyogeny contain a posteriorly located crystalloid body, which is absent in zoites formed by subsequent divisions. Zoites contain posteriorly located amylopectin granules and a relatively large anterior vacuole which is not present in sporozoites. During penetration, the host cell plasmalemma ballooned laterally around the sporozoite creating a large cavity, which later disappeared. Sporozoites and zoites undergoing cell penetration usually exhibit partially empty anterior rhoptries; no changes occur in posterior rhoptries. Lysosomes fuse with the par-asitophorous vacuole surrounding killed sporozoites but not live sporozoites.     

Sophisticated Adaptations of Gregarina cuneata (Apicomplexa) Feeding Stages for Epicellular Parasitism

Background

Gregarines represent a very diverse group of early emerging apicomplexans, parasitising numerous invertebrates and urochordates, and are considered of little practical significance. Recently, they have gained more attention since some analyses showed that cryptosporidia are more closely related to the gregarines than to coccidia.

Methodology/Principal Findings

Using a combined microscopic approach, this study points out the spectacular strategy of Gregarina cuneata for attachment to host tissue and nutrient acquisition while parasitising the intestine of yellow mealworm larvae, and reveals the unusual dynamics of cellular interactions between the host epithelium and parasite feeding stages. Trophozoites of G. cuneata develop epicellularly, attached to the luminal side of the host epithelial cell by an epimerite exhibiting a high degree of morphological variability. The presence of contractile elements in the apical region of feeding stages indicates that trophozoite detachment from host tissue is an active process self-regulated by the parasite. A detailed discussion is provided on the possibility of reversible retraction and protraction of the eugregarine apical end, facilitating eventual reattachment to another host cell in better physiological conditions. The gamonts, found in contact with host tissue via a modified protomerite top, indicate further adaptation of parasite for nutrient acquisition via epicellular parasitism while keeping their host healthy. The presence of eugregarines in mealworm larvae even seems to increase the host growth rate and to reduce the death rate despite often heavy parasitisation.

Conclusions/Significance

Improved knowledge about the formation of host-parasite interactions in deep-branching apicomplexans, including gregarines, would offer significant insights into the fascinating biology and evolutionary strategy of Apicomplexa. Gregarines exhibit an enormous diversity in cell architecture and dimensions, depending on their parasitic strategy and the surrounding environment. They seem to be a perfect example of a coevolution between a group of parasites and their hosts.     

The Fine Structure of the Gregarine Lankesteria culicis Parasitic in the Yellow Fever Mosquito Aedes aegypti

SYNOPSIS. The fine structure of the eugregarine Lankesteria culicis from the larvae of the mosquito Aedes aegypti was examined by light and electron microscopy and compared with that of other gregarines. The cell organelles found in L. culicis included a nucleus, mitochondria, Golgi-complexes, endoplasmic reticulum, vesicles, droplets, granules and lipid bodies.
The surface of L. culicis was composed of a highly differentiated membrane-cortex, differing slightly from that of other eugregarines. This complex was limited by a unit membrane, the plasmelemma, and underlying cortical laminae which appeared to be composed of several layers. The homogeneous electrondense layer present in Pyxinoides balani was greatly diminished or absent in L. culicis.
A series of laminar folds supported by ground substance and longitudinal subpellicular fibrils gave the organism's surface a ridge-like appearance. Permanent cytostome-like openings in the surface, which appeared to be supported by a narrow band of thickened cortex, were present as specializations of the surfacemembrane complex. The structural composition of the parasite appeared quite striking in that it was made up almost entirely of vesicles, granules, and droplets which were absent only in the area of the protomerite. The mitochondria were usually found just beneath the surface or near the nucleus. Mitochondria were also seen in the region of demarcation between the protomerite and deutomerite.