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G S Sliusarev

Publications and source records attributed to G S Sliusarev.

7 recordsLinked to original sources

[The multiyear dynamics of infection and of the distribution of 3 species of Orthonectida in the White and Barents seas].

Annual dynamics and distribution of three Orthonectida species--Intoshia variabili, I. linei, Rhopalura littoralis--have been studied in the invertebrates in the White and Barents seas. Throughout years of observations orthonectids show high stability, constant percent of infection and permanent location of the same spots. Mosaic pattern of their distribution has been revealed. Possible causes of difficulties in finding orthonectids in nature are discussed.

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[Analysis of possible mechanisms of orthonectid emergence from their hosts].

In the present study authors claim that the adult orthonectids can not move through host tissues by themselves. In various species of these enigmatic parasites there are at least two different mechanisms of emission of males and females from the host body. Intoshia linei, the orthonectid from Lineus ruber (Heteronemertini), and Intoshia variabili, the parasite of a flatworm Macrorhynchus crocea, realize the first way of emission. The plasmodium of these species forms tube-like outgrowths, which pierce the host tissues reaching the host body surface. The cytoplasm structure of these outgrowths differs from the cytoplasm of the central mass of plasmodium. Small mitochondria with electron dense matrix, lipid granules and vesicular bodies being common in the central part are absent in these outgrowths. Plasmodial outgrowths reach the host body surface and adult orthonectids move inside them using their cilia and stopping from time to time. The plasmodial outgrowths penetrate the ciliated epithelium, then males and females leave the host. Duration of emission may vary in different species from 6 to 13 days. The second mechanisms of emission is common for the orthonectid parasites of mollusks. Our observations of Rhopalura philinae from the gastropod Philine scabra lead to the conclusion that males and females leave their host practically simultaneously. When the plasmodium attains the terminal stage of its development most of the host entrails are already displaced by plasmodial mass. It causes breaks in host body walls and hence to emission of sexual individuals. During this process, which lasts about 24 hours, the mollusk dies. The same mechanism was observed in Rhopalura littoralis--parasite of the gastropod Onoba aculeus. Our investigations of emission ways reveal that the plasmodium of orthonectids has a potency of directing growth and can form certain structures. The process of forming the plasmodial outgrowths is coordinated in time and space. These outgrowths have certain directions inside the host body and the maturation of sexual individuals is clear related with the development of plasmodium outgrowth system. Our results suggest that forming of plasmodial outgrowths is an element of development of the united and highly integrated system. It is necessary to emphasize the capability of plasmodium to accomplish such morphogenetic transformations. This fact argues that plasmodium is a part of parasite organism and not host cells modified, like some experts supposed.

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[Nuclei in the plasmodium of Intoshia variabili (Orthonectida) as revealed by DAPI staining].

DAPI staining of wholeamounts was used to reveal the parasitic plasmodium of the orthonectid Intoshia variabili in its host, the turbellarian Macrorhynchus crocea. The nuclei of the parasite differ drastically from those of the host in size, morphology, and the estimated DNA content. Our findings indirectly support the idea that the orthonectid plasmodium is a distinct parasitic organism, rather than modified host cells.

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[Muscle formation in the sexual genetation of Intoshia variabili (Orthonectida)].

Muscle formation in Intoshia variabili (Orthonectida) has been studied in the course of development of the sexual (free-living) specimen. The muscle system originates in the early embryogenesis as a distinct continuous layer located between the outer cell layer and the inner cell mass. Later this cell layer disintegrates into separate muscle strips. The presence of a distinct muscle system in Orthonectida and the pattern of its development evidences for placing this group into Triploblastica rather than into Diploblastica.

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[Orthonectida's life cycle].

Analysis of original and literary data permits to conclude that the life cycle in Orthonectida may be characterized as a monohost--monoxenous one, including regular interchange of three generations: asexual and parthenogenetic ones, which are represented by parasitic plasmodiums, and sexual generation, represented by free living and non-feeding males and females or, rarely, hermaphrodites. The sexual individuals are bilaterial, while the parasitic ones are anaxonic. The life cycle of Orthonectida includes the agamic reproduction, apomictic parthenogenesis and sexual reproduction regularly following one another. The life cycle of Orthonectida can be considered as a combination of metagenesis and heterogony. So far, such combination has not been described in any group of metazoan parasites.

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[Symmetry of orthonectids and dicyemids].

The analysis of the general structure of orthonectids shows that free-living sexual specimens are bilaterial, while the parasitic plasmodium is anaxonic. All worm-like stages in the life cycle of dicyemids are characterized by monaxonic heteropolar symmetry, while their infusorioform is bilaterial.

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