A note on the sporogony of Parahaemoproteus velans (= Haemoproteus velans Coatney and Roudabush) (Haemosporidia: Haemoproteidae) in species of Culicoides

1971 ◽  
Vol 49 (3) ◽  
pp. 420-421 ◽  
Author(s):  
R. A. Khan ◽  
A. M. Fallis
Keyword(s):  

Sporogony of Parahaemoproteus velans (= Haemoproteus velans Coatney and Roudabush) was followed in two Culicoides spp. at intervals after feeding on yellow-bellied sapsuckers (Sphyrapicus varius) harboring gametocytes. Cyclical development of the parasite was completed within 96 h at 20 °C. Mature oocysts were small and contained fewer than 50 sporozoites that arose from a single germinal mass. Sporozoites were infective to two uninfected yellow-bellied sapsuckers.

Parasitology ◽  
2009 ◽  
Vol 136 (11) ◽  
pp. 1257-1267 ◽  
Author(s):  
J. THORNHILL ◽  
P. M. Z. COELHO ◽  
P. McVEIGH ◽  
A. MAULE ◽  
A. D. JURBERG ◽  
...  

SUMMARYWe have observed that when cercariae penetrate the skin of mice, there is influx into their tissues of Lucifer Yellow and certain labelled molecules of up to 20 kDa molecular weight. This observation was made using a variety of fluorescent membrane-impermeant compounds injected into the skin before the application of cercariae. This unexpected phenomenon was investigated further by transforming cercariaein vitroin the presence of the membrane-impermeant compounds and examining the distribution by microscopy. In schistosomula derived from this procedure, the nephridiopore and surface membrane were labelled while the pre- and post-acetabular glands were not labelled. The region associated with the oesophagus within the pharyngeal muscle clearly contained the fluorescent molecules, as did the region adjacent to the excretory tubules and the germinal mass. We used cercariae stained with carmine to aid identification of regions labelled with Lucifer Yellow. Although the mechanism of this influx is unclear, the observation is significant. From it, we can suggest an hypothesis that, during skin penetration, exposure of internal tissues of the parasite to external macromolecules represents a novel host-parasite interface.


2018 ◽  
Vol 63 (2) ◽  
pp. 317-324
Author(s):  
Georgii A. Kremnev ◽  
Sergei V. Shchenkov

AbstractMorphology of the daughter sporocysts ofCercaria etgesiiShchenkov, 2017 (Pleurogenidae) has been described according to conventional histological techniques and subsequent 3D reconstruction with Bitplanelmaris® software. Novel data were obtained concerning the spatial organization of the brood cavity of Pleurogenidae daughter sporocysts. It was shown that the laminated structures of the endocyst are lining the brood cavity and carry out its compartmentalisation by formation of the chambers around developing and disintegrating embryos of cercariae. First description of the germinal mass of the Pleurogenidae daughter sporocysts is given. No mitoses in germinal mass were evident although apparent production of the cercariae embryos by the sporocysts take place. The analogous principle of daughter sporocysts morphofunctional organisation was noted for the studied representatives of closely related taxa of trematodes: Pleurogenidae (C.etgesii) and Microphallidae (Microphallus‘pygmaeus’ group).


1950 ◽  
Vol 36 (2) ◽  
pp. 145 ◽  
Author(s):  
William W. Cort ◽  
D. J. Ameel ◽  
Anne Van der Woude
Keyword(s):  

2019 ◽  
Vol 94 ◽  
Author(s):  
I.M. Podvyaznaya ◽  
A.A. Petrov ◽  
K.V. Galaktionov

Abstract Bunocotyle progenetica is a hemiuroid digenean whose sexual adults become fully developed and lay their eggs inside the rediae in the molluscan host. In this study, the fine structure of the germinal mass, brood cavity and birth canal in the B. progenetica rediae was examined using transmission electron and confocal microscopy. The large germinal mass attached to the body wall has a cellular composition typical for this organ. The characteristic traits of this germinal mass are weakly developed supporting tissue and the presence of deep lacunae opening into the brood cavity. These lacunae presumably participate in feeding the deeply lying embryos and facilitate their release into the brood cavity. The germinal mass is also characterized by intensive degeneration of cellular elements, which may represent a mechanism controlling the offspring number, limited in this species by the size of the redial brood cavity. The brood-cavity lining consists of flattened cells bearing lamellar projections and is connected anteriorly with the epithelium of the birth canal. The brood-cavity musculature, which is well developed in other hemiuroid digeneans, is significantly reduced in B. progenetica, most likely because their cystophorous cercariae remain inside the rediae, removing the need for muscle contractions pushing them through the brood cavity. The birth canal comprises three regions distinguished by the structure of the lining and muscle arrangement. The comparison of rediae of B. progenetica with parthenitae of other digeneans has shown that the organization of the redial reproductive apparatus in this species may have been influenced by life-cycle modification.


1918 ◽  
Vol s2-63 (250) ◽  
pp. 175-196
Author(s):  
J. BRONTÉ GATENBY

Before entering upon any discussion or comment on the above description of Polyembryony, a summary of the main facts known will be given. (1) Polyembryony in the Hymenoptera parasitica is process whereby the single egg, instead of producing a single embryo, often produces several score or more. (2) The polyembryonic Hymenoptera are generally small insects about 1 mm. in length. (3) The polyembryonic parasite lays from one to ten or more eggs in the ovum of the host. (4) This oviposition does not kill the host eggs. Larvæ hatch from the latter in the normal way, but contain the eggs of the parasite, generally in the hæmocoæl cavity. (5) The parasite's egg gives off polar bodies, and may or may not be fertilised in the normal way. (6) The polar bodies rest for a time, but then break into activity, forming an actively growing mass, or collection, of nuclei. (7) That part of the egg cytoplasm containing the segmentation nucleus separates off from the outer part containing the active polar nuclei, and the germ-cell determinant goes to the former, but later becomes absorbed and lost to sight. (8) The polar cytoplasm or ooplasm containing the polar nuclei forms an investing sheath around the contained embryonic ooplasm, which later gives rise to the embryos. The polar ooplasm nourishes the inner embryonic mass and acts as an amnion or placenta. Hence the name trophoamnion. (9) The nuclei of the tropho-amnion derived from the original polar body nuclei become very numerous by division, and the tropho-amniotic cytoplasm becomes very granular in the region of the nuclei. (10) Certain cells of the embryo, either hæmolymph or fat cells or both, form an outer covering to the parasitic germinal mass. This host-covering later becomes much stretched and epithelial in character. In some forms it is not well developed. (11) The primary embryonic cell separated off at the time when the polar nuclei begin to become active, has already divided many times to give rise to many germinal masses. The parasitic body lying inside the host hæmocoel. may now be called a polygerm. (12) The polygerminal embryonic masses, keeping on dividing till as many as a hundred or more masses may be produced, later become constricted into areas each containing an embryonic mass surrounded by two membranes, the outer host-epithelial and the inner tropho-amniotic layer. (13) The shape of the entire polygerminal mass differs in different forms. In some it is a ramifying cylindrical body, in others a shapeless mass, constricted here and there by the outer membranes. (14) Bach separate germinal mass is now a spherical or ovoid morula containing a score or more cells. The latter keep dividing. (15) The embryonic or germinal mass now begins to differentiate further; it loses its sub-spherical shape and becomes elongate, while dorsal, ventral, and lateral sides of the future embryo can be distinguished. (16) The stomodæum and proctodæum are formed by invaginations of the two extreme ends of a ventral groove. The ectoderm is formed by a rearrangement of the outer cells of the morula. The endoderm and mesoderm are formed in situ by a modification of the more centrally-placed cells of the embryo. (17) The larvæ at a later stage break away from their membranes and are free-living for a time. They later eat up nearly everything in the host-caterpillar's body and then pupate inside (in some cases, however, apparently outside) the body of their host. In this review I have not so far given any data with regard to the sexes of parasites emerging from one caterpillar. Broods may be purely male or female, or mixed. In Patterson's cases 55 per cent, of all broods were female. Moreover, the average number of females emerging from a single carcase is 198 as compared with 175 for males. Some of the mixed broods doubtless arose from two or more eggs, fertilised and unfertilised; but Patterson makes the interesting suggestion that such mixed broods may also arise from a single fertilised egg by a process of disjunction of the sex chromosome during early cleavage stages (13). As far as is known fertilised eggs produce females, unfertilised males.


1994 ◽  
Vol 68 (2) ◽  
pp. 135-141 ◽  
Author(s):  
Y. Manga-González ◽  
C. González-Lanza ◽  
I. Kanev

AbstractTo study the distribution of Lymnaea truncatula in the Porma river basin (León, NW Spain) and its helminth fauna, malacological samplings were carried out at 66 points in the basin and the presence of these molluscs was detected in 31. To trace the dynamics of this mollusc population and the prevalence and intensity of its infection by trematodes, malacological samplings were made at fortnightly intervals over two years at five locations, situated in the upper and middle regions of the river Porma basin. To confirm the identity of the larval stages found in the molluscs, second intermediate and/or definitive hosts, depending on the trematode species, were experimentally infected to complete the life cycles. Two different species of Plagiorchiidae and one of Notocotylidae were identified. The infection prevalence of Plagiorchis elegans for the 6291 specimens of L. truncatula examined was 2.8% and infection was observed in snails collected in 7 of the 31 sample localities. This parasite was found in all months of the year, with the highest prevalence observed in July and October. When the corrected frequency values were considered, a slightly positive relationship was observed between the infection prevalence and the latter months. The highest percentages of snails harbouring immature sporocysts were detected in March and June–July, while the highest percentages with sporocysts containing mature cercariae were observed in spring and at the end of summer–autumn, and cercarial shedding in the latter. Of the 6291 L. truncatula examined 0.3% were infected by sporocysts of Opisthioglyphe ranae. The infection was detected in only one locality, in four months of the year, with the highest prevalence in May. Notocotylus neyrai was found in 2.6% of the 6291 mollusc specimens checked and was collected from 12 of the 31 localities. The highest prevalence was observed in October, April and July and the corrected frequency values reveal a positive relationship between the infection prevalence and those three months. The highest percentage of molluscs harbouring rediae of N. neyrai with germinal mass was found in April and September–October. On the other hand, rediae with mature cercariae were present in almost every month, but we only observed cercarial shedding in October and March. The L. truncatula infection prevalence by P. elegans, O. ranae and N. neyrai increased with the size of the molluscs. Double infection was only observed in four snails: one harboured O. ranae and N. neyrai and three F. hepatica and P. elegans.


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