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L Euzet

Publications and source records attributed to L Euzet.

At least 37 records · Page 2Linked to original sources
PubMed1993

Diversity and specificity in cestodes of the genus Moniezia: genetic evidence.

Electrophoretic study of two species of Moniezia cestodes, M. expansa and M. benedeni, sampled in African (Senegal) domesticated ruminants, revealed a complex of species and a degree of specificity more pronounced than that previously described. The status of the different species is validated by the probable occurrence of within species cross-mating. A European origin is suggested for M. expansa due to identical isoenzyme patterns in cestodes from France, whereas some atypical individuals may be derived from wild African ruminants.

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PubMed1983

[Ligophorus parvicirrus n. sp. (Monogenea, Ancyrocephalidae), parasite of Liza ramada (Risso, 1826) (Teleostei, Mugilidae)].

Ligophorus parvicirrus, a new gill parasite of Liza ramada is described with its taxonomic position. The diagnosis of the genus Ligophorus Euzet and Suriano, 1977 is reviewed. The branchial distribution of Ligophorus parvicirrus is given and its microhabitat defined. The effects of a competition between this species and Ligophorus imitans Euzet and Suriano, 1977, another gill parasite of L. ramada are shown.

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PubMed1981

[Comparative fine structure of the cestode spermatozoon. Relationship to phylogenesis].

The comparison of the ultrastructure of spermatozoa in Cestodes from seven different orders shows that they have the same general pattern of organization. The main common features are following: (a) a long thread-like body; (b) an elongated nucleus; (c) cortical microtubules underlying plasma membrane; (d) the absence of mitochondria and of a typical acrosome. The mode of spermatozoon differentiation indicates an inversion of the polarity. The number of axonemes of the 9 + "1" pattern, characteristic of the platyhelminthes, allow us to distinguish two types of spermatozoa among cestodes: --The "two-axonemes"-type is considered as primitive as it has also been found in the free-living platyhelminths. This type has been observed in the Pseudophyllidea, Proteocephalidea, Tetrarhynchidea and Tetraphyllidea (Onchobothriidae). --The "one-axoneme"-type has been found in the Cyclophyllidea, Caryophyllaeidea, Diphyllidea and Tetraphyllidea (Phyllobothriidae). It has been proved that the one axoneme type of the spermatozoon, observed in Tetraphyllidea, Phyllobothriidae arises from the two axoneme type by early abortion of the second axoneme. In all the tetraphyllidean species studied so far, we found an helicoidal body forming so-called "crested body" or "spiral crest" at the proximal end of the spermatozoon, which is opposite to the nuclear part. This division of the cestodes into two groups, according to the number of axonemes in the spermatozoon is compared with the phylogenetic diagrammes of Cestoda proposed by Freeman (1973) and Euzet (1974). As result, two hypothesis can be forwarded to explain the relationships between the Tetraphyllidea, Proteocephalidea and Cyclophyllidea. The importance of data on the cestode spermatozoa as a criterion in analysis of cestode phylogenesis is drawn and discussed.

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PubMed1976

[A new monogenean parasite (Bouixella n. g.) in the Mormyridae (teleosts) of Benin].

Study of the Monogenean gill parasites occuring in the Mormyrid fish from Benin (Africa). Description of a new genus, Bouixella. It differs from the other Ancyrocephalidae by the number (4) of cross bars between the haptoral hamuli. This new genus seems to bee specific of the mormyridae among which a new example of simultaneous gill parasitism by congeneric species is reported.

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PubMed1975

[Ultrastructure of nephridial systems in cyclophyllidean cestoda: Catenotaenia pusilla (Goeze, 1782), Hymenolepis diminuta (Rudolphi, 1819) and Inermicapsifer madagascariensis (Davaine, 1870) Baer, 1956].

Electron microscopic study of nephridial systems in three cyclophyllidean cestodes indicates a resemblance in their ultrastructure. The walls of longitudinal, transverse and collecting ducts show a very similar pattern of organization. The surface of the anucleate epithelium lining the ducts is developed into microvilli. A relatively thick layer of fibrillar tissue underlies the basal membrane of the microvillar epithelium. The nucleated portions or "pericaryons", situated between the parenchymal cells, are directly connected with epithelium by cytoplasmic prolongations. The canalicular lumen extends through a single series of cells curved into a ring. The epithelial surface of the canalicular wall is developed into short, densly staining microvilli and the immediately underlying fibrillar tissue appears very compact. The cilia were never observed in any of the above ducts. The ultrastructure of protonephridia proper is comparable with those already described in other cestodes. There is a close association between the flame-cell and the cancalicular ending, enlarged into a nephridial funnel. A single row of nephridial rods of the flame-cell is surrounded by a row of digitiform prolongations of the nephridial funnel border. The prolongations alternate with the rods and their interlocking pattern appears clearly in cross-sections. A series of minute pores or "nephrostomes" providing a direct contact between the nephridial chamber and intercellular space of the paranchyma was shown. The problem of classification and definition between the "closed" protonephridia and open metanephridia is discussed. The structural unity of protonephridia in different groupes of Platyhelminthes is reviewed. The different number of flagella within the "flames" of different cestodes is compared and analyzed. The ultrastructural characteristics of duct-wall epithelium provides some confirmation of its high metabolic activity.

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PubMedDate not supplied

[Embryonic development of 2 Phyllobothriidae (Cestoda: Tetraphyllidea)].

Caulobothrium longicolle (Linton, 1890) and Phyllobothrium gracile (Weld, 1855) (Cestoda: Tetraphyllidea, Phyllobothriidae) have the same embryonic development with the following characteristic data: --a small number of vitelline cells (2 or 3) pass with the zygote in the ootype;--a non operculate thin egg-shell;--the entire and equal zyhote cleavage following by unequal divisions leading to the formation of four blastomere types (Macromeres, secondary Macromere, Mesomeres and Micromeres);--the differentiation of two syncytial embryonic envelopes during the preoncospheral phase. The outer envelope encloses the vitelline material remnant and three Macromeres among which the secondary Macromere. The inner envelope or embryophore, originates from five or six Mesomeres;--the presence of the oncospheral membrane;--the Phyllobothriidae ontogenesis is similar to that of the Onchobothriidae. By their embryonic features, the Tetraphyllidea are close to the Cyclophyllidea. This similarity suggests a phylogenic relationship between those two Cestoda orders.

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PubMedDate not supplied

[Embryonic development of three Cestoda from the genus Acanthobothrium (Tetraphyllidea, Onchobothriidae) (author's transl)].

The embryonic development from the egg to the oncosphere is examined in three Cestoda: Acanthobothrium coronatum (Rud., 1819), Acanthobothrium filicolle, Zschokke, 1888 and Acanthobothrium zschokkei Baer, 1948 (Tetraphyllidea, Onchobothriidae). The three ontogeneses have in common the following data: -- Two vitelline cells pass with the zygote into the ootype where a thin shell is formed out of a material which comes from the vitelline cells. -- At first the cleavage is equal, then it becomes unequal resulting in the formation of four types of blastomeres: macromere, secondary macromere, mesomere and micromere. -- The preoncospheral phase is characterized first by the blastomere multiplication and later by their decreasing number and differentiation. -- The embryonic envelopes are formed within the shell. The vitelline layer includes the cytoplasm, a vitelline nucleus and possibly the secondary macromere, the nucleus of which always lies against the outer membrane of this envelope. The syncytial embryophore develops from mesomeres coming from the embryo. -- The oncosphere is limited by its owm membrane whose posterior region seems to double in order to form a kind of cap bending over the six hook tips. The final number of embryonic hexacantha cells is relatively low.

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