Spermiogenesis and spermatozoon ultrastructure of the paruterinid cestode Notopentorchis sp. (Cyclophyllidea)

Ultrastructural characters of the spermiogenesis and mature spermatozoon of Notopentorchis sp. (Cestoda, Cyclophyllidea, Paruterinidae), a parasite from Apus affinis (Aves, Apodiformes, Apodidae) from Gabon, are described by means of transmission electron microscopy. Cytochemical analysis for detection of glycogen was applied. Vestigial striated roots associated with the two centrioles are present in the zone of differentiation. The spermiogenesis is characterized by an external growth of free flagellum followed by a proximodistal fusion of the latter with cytoplasmic protrusion, thus, corresponding to the cestode spermiogenesis of the type III pattern described by Ba and Marchand (Mem. Mus. Natl. Hist. Nat. 166:87-95, 1995). In the final stage of spermiogenesis, a single crested body appears at the base of the forming spermatozoon. The mature spermatozoon of Notopentorchis sp. is filiform and tapering at both extremities. It consists of five regions differing in their ultrastructural characteristics. The anterior extremity of the mature spermatozoon is characterized by the presence of an apical cone and a single crested body. The cytoplasm contains one axoneme of 9 + "1" type of the trepaxonematan Platyhelminthes, a periaxonemal sheath, a layer of twisted cortical microtubules, transverse intracytoplasmic walls, and granules of glycogen. The nucleus is coiled in spiral around the axoneme. The posterior extremity of the spermatozoon is characterized by the presence of electron-dense material. This structural organization corresponds to the morphology of cestode spermatozoon of type VII as defined by Levron et al. (Biol Rev 85: 523-543, 2010). The comparison of the results with those of the two previous studies on paruterinids suggests that several characters of the spermiogenesis and the mature spermatozoon are invariable, i.e. the type III spermiogenesis and the presence of vestigial striated roots, a single crested body, a periaxonemal sheath, and intracytoplasmic walls. The main differences of the sperm cells among members of this family are the lack of dense granules (as in Triaenorhina rectangula) and the presence of electron-dense material in the posterior extremity of the spermatozoon (as in Notopentorchis sp.).     

Ultrastructure of spermiogenesis and mature spermatozoon of Angularella beema (Clerc, 1906) (Cestoda, Cyclophyllidea, Dilepididae)

The ultrastructure of the spermiogenesis of a dilepidid cestode species is described for the first time. The spermiogenesis of Angularella beema is characterised by absence of both flagellar rotation and proximodistal fusion. The differentiation zone is surrounded by cortical microtubules and is delimited by a ring of arching membranes. It contains two centrioles, one of which develops the axoneme that grows directly into the elongating cytoplasmic protrusion. This pattern of spermiogenesis was described as the Type IV spermiogenesis of cestodes. Among cestodes, similar pattern of spermiogenesis is known in the family Hymenolepididae and in some representatives of the family Anoplocephalidae. The mature spermatozoon of A. beema consists of five regions differing in their ultrastructural characteristics. It is characterised by the presence of cortical microtubules (spirally arranged at angle of 30–40° to the spermatozoon axis) and a single crested body. There is a periaxonemal sheath in certain parts of the spermatozoon as well as glycogen-like granules between the periaxonemal sheath and the cortical microtubules. The comparisons of the mature spermatozoon of A. beema with those of other two dilepidid species (Dilepis undula and Molluscotaenia crassiscolex) demonstrate some variation within the family: presence of periaxonemal sheath in A. beema and D. undula and its absence in M. crassiscolex; presence of electron-dense rods in D. undula and their absence in A. beema.     

Ultrastructure of the spermatozoon of Dollfusiella spinulifera (Beveridge and Jones, 2000) Beveridge, Neifar and Euzet, 2004 (Trypanorhyncha, Eutetrarhynchidae)

The ultrastructural organization of the mature spermatozoon of the trypanorhynch cestode Dollfusiella spinulifera is described. The spermatozoon is a long filiform cell, tapered at both ends, which lacks mitochondria. Its cytoplasm contains (1) two axonemes of different lengths of the 9+‘1’ pattern of trepaxonematan Platyhelminthes, (2) two rows of parallel cortical microtubules, each of which is adjacent to the opposite sides of the plasma membrane, (3) the nucleus, and (4) glycogen in the form of both α-glycogen rosettes and β-glycogen particles. Unlike the majority of cestode spermatozoa, the spematozoon of D. spinulifera lacks crested bodies and periaxonemal sheath. In view of the present results, the postulated synapomorphic value of crested bodies for the Eucestoda is questioned.     

Spermatozoon cytoarchitecture of Amphilina foliacea (Platyhelminthes, Amphilinidea)

The mature spermatozoon of Amphilina foliacea Rudolphi, 1819 has been examined using transmission electron microscopy. The male gamete is filiform and tapered at both extremities. Its moderately electron-dense cytoplasm possesses two parallel axonemes of unequal lengths with the 9?+?“1” trepaxonematan pattern, a mitochondrion, a nucleus, parallel cortical microtubules, four electron-dense attachment zones, and electron-dense glycogen granules. A crested body is absent. The anterior extremity of the cell exhibits a single axoneme. The anteriormost cortical microtubules have been observed with the appearance of the second axoneme. The number of cortical microtubules reaches a maximum (up to 25) in the nucleated region III of the spermatozoon. A single mitochondrion extends from the middle of region II to the end of region III of the cell. Both axonemes have become disorganized in a similar way: the axonemal doublets disappear first, followed by the central core. The nucleus is surrounded by a few cortical microtubules in the proximal part of region V. In the distal extremity of the mature spermatozoon, there is only the nucleus. Differences of spermatozoon ultrastructure within Amphilinidea and other Neodermata are discussed.     

Spermiogenesis and sperm ultrastructure of Valipora mutabilis Linton, 1927 (Cestoda, Cyclophyllidea, Gryporhynchidae)

This is the first ultrastructural study of the spermiogenesis and the mature spermatozoon of a cyclophyllidean cestode of the family Gryporhynchidae. The spermiogenesis of Valipora mutabilis begins with the formation of a differentiation zone delimited by arching membranes and containing two centrioles. One of the centrioles develops an axoneme that grows directly into the cytoplasmic protrusion. The other centriole remains situated in a cytoplasmic bud and is subsequently aborted (type IV of cestode spermiogenesis). The mature spermatozoon of V. mutabilis is a filiform cell, tapered at both extremities and lacks mitochondria. The anterior extremity is characterised by the presence of an apical cone and a single helicoidal crested body. The axoneme is of 9 + ‘1’ trepaxonematan pattern, with a periaxonemal sheath. The cortical microtubules are twisted at an angle of about 45° to the spermatozoon axis. The nucleus is electron dense and spirally coiled around the axoneme. The cytoplasm is electron lucent and contains numerous granules of electron-dense material. In contrast to a recent opinion for close phylogenetic relationships, these ultrastructural data demonstrate the distant position between gryporhynchids and the family Taeniidae. The most similar pattern in the ultrastructure of the spermiogenesis and the mature spermatozoon has been described for dilepidids, some hymenolepidids and some anoplocephalids.     

Ultrastructure of spermiogenesis and the spermatozoon in the genus Joyeuxiella Fuhrmann, 1935 (Cestoda,Cyclophyllidea, Dipylidiidae): comparative analysis of J. echinorhynchoides (Sonsino, 1889) and J. pasqualei (Diamare, 1893)

This paper describes the ultrastructure of spermiogenesis and the mature spermatozoon of two Dipylidiidae cestodes, Joyeuxiella echinorhynchoides and J. pasqualei. In both species, spermiogenesis follows the type III described by Bâ and Marchand for the cyclophyllideans. Nevertheless, it is interesting to note the presence of striated roots associated with the centrioles. The spermatozoon presents the same ultrastructural features in J. echinorhynchoides and J. pasqualei. The apical cone in the anterior extremity of the sperm is more than 2.0 m long in both J. echinorhynchoides and J. pasqualei. Both species present a single crest-like body, 150 nm thick in J. echinorhynchoides and 75 nm thick in J. pasqualei. The cortical microtubules are spiralled at an angle of 40–45° to the spermatozoon axis in both Joyeuxiella species. A periaxonemal sheath and glycogen granules are also described in the mature sperm. We also describe, for the first time, the disposition of glycogen granules in two opposed and spiralled cords in cestodes and the formation of the periaxonemal sheath in the final stage of spermiogenesis.     

Ultrastructural study of the spermatozoon of Taenia taeniaeformis (Batsch, 1786) (Cestoda, Cyclophyllidea, Taeniidae), an intestinal parasite of Felis catus from La Palma (Canary Islands, Spain)

The ultrastructural characters of the mature spermatozoon of Taenia taeniaeformis are described by means of transmission electron microscopy. Materials were obtained from a naturally infected road-killed cat (Felis catus) from La Palma (Canary Islands, Spain). The mature spermatozoon of T. taeniaeformis is a filiform cell, which is tapered at both extremities and lacks mitochondria. It is characterised by the presence of (1) a single spirallised crested body about 140 nm thick, (2) a single axoneme of the 9+’1’ pattern of trepaxonematan Platyhelminthes, (3) a twisted (40°) layer of submembranous cortical microtubules, (4) a periaxonemal sheath surrounding the axoneme, (5) transverse intracytoplasmic walls and (6) a spirallised nucleus encircling the axoneme. The mature spermatozoon of T. taeniaeformis is also characterised by the presence of an apical cone in its anterior extremity and by the disorganisation of the axoneme in its posterior extremity. The ultrastructural characters of the mature spermatozoon of T. taeniaeformis are compared with those of other cestodes studied to date, with particular emphasis on other representatives of the family Taeniidae.     

Spermiogenesis and sperm ultrastructure of the pseudophyllidean cestode Triaenophorus nodulosus (Pallas, 1781)

Spermiogenesis and ultrastructure of the spermatozoon of the pseudophyllidean cestode Triaenophorus nodulosus (Pallas, 1781), a parasite of pike Esox lucius, has been studied by transmission electron microscopy. Spermiogenesis involves firstly the formation of a zone of differentiation with two centrioles associated with striated roots, and an intercentriolar body between them, subsequent growth of the two flagella of unequal length, and a formation of a median cytoplasmic process exhibiting patches of dense material. The nucleus penetrates into spermatid body after flagellar rotation and proximo-distal fusion has started. The mature spermatozoon of T. nodulosus is filiform and contains two axonemes of 9+“1” pattern of the Trepaxonemata, nucleus, cortical microtubules parallel to the spermatozoon axis, and electron-dense granules. The anterior extremity of the gamete contains a single centriole surrounded by numerous electron-dense tubular structures exhibiting spiral arrangement and giving rise to lateral projections, which correspond to the crested body. When the crested body disappears, the spiral pattern of electron-dense tubular structures is changed into a ring, persisting until the centriole of the second axonemes appears. This structure of the crested body of T. nodulosus is unique among the Eucestoda.     

Spermiogenesis and spermatozoon of the tapeworm <Emphasis Type="Italic">Parabothriocephalus gracilis</Emphasis> (Bothriocephalidea): Ultrastructural and cytochemical studies

Spermiogenesis and spermatozoon ultrastructure of the tapeworm Parabothriocephalus gracilis were described using transmission electron microscopy (TEM). Spermiogenesis is characterized by the formation of a zone of differentiation with two centrioles associated with striated rootlets, and an intercentriolar body between them. The two flagella undergo a rotation of 90° until they become parallel to the median cytoplasmic extension with which they fuse. Electron-dense material is present in the apical region of the zone of differentiation in the early stages of spermiogenesis. This electron-dense material is characteristic for the orders Bothriocephalidea and Diphyllobothriidea. The mature spermatozoon contains two axonemes of the 9 + ‘1’ trepaxonematan pattern, nucleus, parallel cortical microtubules and electron-dense granules of glycogen. The anterior extremity of the spermatozoon exhibits a single helical electron-dense crested body 130 nm thick. One of the most interesting features is the presence of a ring of cortical microtubules surrounding the axoneme. This character has been reported only for species of the order Bothriocephalidea and may be unique in this cestode group.     

Spermiogenesis and spermatozoon ultrastructure of the bothriocephalidean cestode <Emphasis Type="Italic">Clestobothrium crassiceps</Emphasis> (Rudolphi, 1819), a parasite of the teleost fish <Emphasis Type="Italic">Merluccius merluccius</Emphasis> (Gadiformes: Merlucciidae)

Spermiogenesis and the ultrastructure of the spermatozoon of the bothriocephalidean cestode Clestobothrium crassiceps (Rudolphi, 1819), a parasite of the teleost fish Merluccius merluccius (Linnaeus, 1758), have been studied by means of transmission electron microscopy. Spermiogenesis involves firstly the formation of a differentiation zone. It is characterized by the presence of two centrioles associated with striated rootlets, an intercentriolar body and an electron-dense material in the apical region of this zone. Later, two flagella develop from the centrioles, growing orthogonally in relation to the median cytoplasmic process. Flagella then undergo a rotation of 90° until they become parallel to the median cytoplasmic process, followed by the proximodistal fusion of the flagella with the median cytoplasmic process. The nucleus elongates and afterwards it migrates along the spermatid body. Spermiogenesis finishes with the appearance of the apical cone surrounded by the single helical crested body at the base of the spermatid. Finally, the narrowing of the ring of arched membranes detaches the fully formed spermatozoon. The mature spermatozoon of C. crassiceps is filiform and contains two axonemes of the 9 + “1” trepaxonematan pattern, a parallel nucleus, parallel cortical microtubules, and electron-dense granules of glycogen. The anterior extremity of the gamete exhibits a short electron-dense apical cone and one crested body, which turns once around the sperm cell. The first axoneme is surrounded by a ring of thick cortical microtubules that persist until the appearance of the second axoneme. Later, these thick cortical microtubules disappear and thus, the mature spermatozoon exhibits two bundles of thin cortical microtubules. The posterior extremity of the male gamete presents only the nucleus. Results are discussed and compared particularly with the available ultrastructural data on the former “pseudophyllideans”. Two differences can be established between spermatozoa of Bothriocephalidea and Diphyllobothriidea, the type of spermatozoon (II vs I) and the presence/absence of the ring of cortical microtubules.     

Spermatological characters of the caryophyllidean cestode <Emphasis Type="Italic">Khawia sinensis</Emphasis> Hsü, 1935, a carp parasite

Spermatological characters of the caryophyllidean tapeworm Khawia sinensis (Lytocestidae), a carp parasite, have been investigated for the first time. The process of the spermatozoon formation corresponds in basic pattern to that of Khawia armeniaca (Bruňanská and Poddubnaya, Parasitol Res 99: 449–454, 2006). The presence of dense material at the early stages of spermiogenesis, the intercentriolar body, flagellar rotation (free flagellum plus flagellar bud), and a complete proximodistal fusion have been reported. In addition, it was shown that the developing spermatids may exhibit a free flagellum distally. The unipartite young spermatid and/or mature spermatozoon of K. sinensis consist of one axoneme of the 9 + “1” trepaxonematan pattern, nucleus, and cortical microtubules. These components are situated in cytoplasm, which is either electrolucent (young spermatid) or moderately electrodense (mature spermatozoon). The crested body is absent. The proximal extremity of the male gamete of K. sinensis contains a centriole and a few (up to six) cortical microtubules arranged in a semicircle. The number of cortical microtubules increases distally and reaches maximum (up to 15) in the middle part of the filiform cell, which contains the nucleus. The posterior extremity of the mature spermatozoon exhibits elements of the disorganized axoneme. The ultrastructural characteristics of spermiogenesis and the mature spermatozoon of K. sinensis support basal position of the Caryophyllidea (and Spathebothriidea) relative to other eucestode orders.     

Ultrastructure of the spermatozoon of the proteocephalidean cestode <Emphasis Type="Italic">Proteocephalus torulosus</Emphasis> (Batsch, 1786)

The fine structure of the mature spermatozoon of the proteocephalidean tapeworm Proteocephalus torulosus, a parasite of cyprinid fishes, was studied by transmission electron microscopy for the first time. The mature spermatozoon of P. torulosus is filiform and tapered at both extremities. It contains two axonemes of the 9+"1" type and of unequal length. The anterior extremity of the spermatozoon bears a helicoidal crested body approximately 100 nm thick. Cortical microtubules of two types lie parallel to the spermatozoon axis. The nucleus is a fine cord of condensed chromatin. The slightly electron-dense cytoplasm contains electron-dense granules in regions II and III of the spermatozoon. The anterior and posterior extremities of the spermatozoon contain a single axoneme. The mature spermatozoon of P. torulosus differs from that of other Proteocephalusspecies in the presence of a single crested body and in the morphology of its posterior end.     

Ultrastructure of the spermatozoon of <Emphasis Type="Italic">Calliobothrium verticillatum</Emphasis> (Cestoda,Tetraphyllidea, Oncobothriidae)

The ultrastructure of the spermatozoon of Calliobothrium verticillatum (Cestoda, Tetraphyllidea, Oncobothriidae) parasite of the smoothhound shark, Mustelus mustelus L. (Pisces, Carcharhiniformes), was studied by transmission electron microscopy. This spermatozoon presents five regions characterized by several ultrastructural elements: an apical cone, a crested body, two axonemes of 9 + “1” pattern, electron-dense granules, a nucleus and cortical microtubules. In the present study, three of these features were the subject of a detailed attention. The first is the presence of two axonemes, which confirms that the Tetraphyllidea, Oncobothriidae possess two axonemes whereas the Tetraphyllidea, Phyllobothriidae possess only one axoneme. The second is the presence of one crested body, a criterion homogeneous in the Tetraphyllidea but heterogeneous among the different orders of Cestoda. The third is the number and the disposition of cortical microtubules. These three criteria seem to be interesting for phylogeny.     

Ultrastructure of the spermatozoon of the diphyllobothriidean cestode Cephalochlamys namaquensis (Cohn, 1906)

This contribution provides the first ultrastructural and cytochemical data on the mature spermatozoon of a diphyllobothriidean cestode belonging to the family Cephalochlamydidae. The mature spermatozoon of Cephalochlamys namaquensis (Cohn, 1906), a parasite of the African clawed frog, Xenopus laevis (Daudin, 1802), from southern California, USA, has been examined using transmission electron microscopy and cytochemical staining with periodic acid-thiosemicarbazide-silver proteinate for glycogen. The male gamete is a filiform cell tapered at both extremities. Its moderately electron-dense cytoplasm possesses two parallel axonemes of unequal lengths with a 9?+?"1" trepaxonematan pattern, a nucleus, parallel cortical microtubules, four electron-dense plaques/attachment zones, and electron-dense granules of glycogen. The crested body is absent. The anterior extremity of the cell exhibits a centriole surrounded by a semiarc of four parallel cortical microtubules. The number of cortical microtubules reaches its maximum (up to 37) at the beginning of the anucleated two-axoneme region II of the spermatozoon. In contrast to other diphyllobothriideans, a small membranous element appears in the anucleated region II. In addition, the nucleus is surrounded by a few cortical microtubules in region V. The distal extremity of the mature spermatozoon exhibits only one nucleus. Variations of spermatozoa ultrastructural characters within diphyllobothriideans as well as other Eucestoda are discussed.     

Ultrastructure of the spermatozoon of Dipylidium caninum (Cestoda, Cyclophyllidea, Dilepididae), an intestinal parasite of Canis familiaris

We report for the first time the ultrastructure of the spermatozoon of a Dilepididae cestode. The mature spermatozoa of Dipylidium caninum is filiform and tapered at both ends and lacks mitochondria. The anterior extremity exhibits an apical cone of electron-dense material measuring about 600 nm in length and a single helicoidal crested-like body that is 150 nm thick. This single crested-like body is spiralized at an angle of about 40° to the spermatozoon axis. The axoneme, showing the 9 + “1” pattern of the Platyhelminthes, lacks a periaxonemal sheath. The cortical microtubules constitute a continuous, submembranous, electron-dense material, and they are also twisted at an angle of about 40° to the spermatozoon axis. Moreover, the nucleus is coiled in a helix around the axoneme, which is centrally located throughout its length. We demonstrate for the first time the presence of peripheral microtubules twisted to the spermatozoon axis up to the posterior extremity of the gamete. Received: 2 October 1996 / Accepted: 31 October 1996     

Ultrastructure of the spermatozoon of <Emphasis Type="BoldItalic">Bothriocephalus claviceps</Emphasis> (Cestoda,Pseudophyllidea): a parasite of <Emphasis Type="BoldItalic">Anguilla anguilla</Emphasis> (Fish,Teleostei)

The mature Bothriocephalus claviceps spermatozoon is filiform and tapered at both extremities. It contains two axonemes of unequal lengths of the 9+“1” pattern of the trepaxonemata. The anterior extremity exhibits an apical cone of an electron-dense material about 6.6 μm long by 0.2 μm wide at its base and a crest-like body making an angle of about 40° with the spermatozoon axis. It is spiralized around the whole extremity of the spermatozoon. The nucleus is a cord of electron-dense material that interposes itself between the two axonemes. The cortical microtubules are of two types: hollow-centred and electron-dense centred. The cytoplasm is slightly electron dense and contains numerous electron-dense granules in regions III, IV, and V of the spermatozoon. The anterior and posterior extremities of the spermatozoon contain a single axoneme. The presence of an apical cone of the electron dense material has never, to our knowledge, been reported in the Pseudophyllidea. In addition, we show for the first time the existence of a crested body in the Bothriocephalidae.     

Spermatological characters of <Emphasis Type="Italic">Acanthobothrium crassicolle</Emphasis> Wedl, 1855 (Tetraphyllidea,Onchobothriidae), a parasite of the common stingray <Emphasis Type="Italic">Dasyatis pastinaca</Emphasis>

We describe the spermiogenesis process and the ultrastructural characters of the spermatozoon of Acanthobothrium crassicolle by means of transmission electron microscopy, including cytochemical analysis for glycogen. Spermiogenesis in A. crassicolle begins with the formation of the differentiation zone that contains two centrioles associated with striated rootlets and an intercentriolar body. The latter is formed by one electron-dense layer. The centrioles develop into two free flagella that first grow orthogonally to a median cytoplasmic process and then undergo flagellar rotation becoming parallel to that median cytoplasmic process. After flagellar rotation only one of the flagella completes its growth and both short and long flagella undergo proximodistal fusion with the median cytoplasmic process. In the final stages of spermiogenesis, the nucleus becomes filiform and migrates into the spermatid body. Later, the ring of arched membranes constricts and the spermatozoon is liberated from the residual cytoplasm. The ultrastructural organization of the spermatozoon of A. crassicolle follows the general pattern of spermatozoa of the other Tetraphyllidea-Onchobothriidae species, but exhibits some differences. It is filiform, tapered at both extremities and lacks mitochondrion. It contains two axonemes of unequal length showing the 9 + “1“ pattern of Trepaxonemata, a nucleus, parallel cortical microtubules and electron-dense granules of glycogen. The anterior extremity of the male gamete contains a single crested body surrounding a thin and long apical cone. This type of apical cone has never been described in a tetraphyllidean spermatozoon. Another particularity is the presence of a single electron-dense microtubule at the vertex of the crested body.     

Ultrastructure of the spermatozoon of Taeniarhynchus saginatus (syn. Taenia saginata) (Goeze, 1782) Weinland, 1858 (Cestoda, Taeniidae) an intestinal parasite of human

The mature Taeniarhynchus saginatus spermatozoon exhibits an apical cone of electron-dense material and one helicoidal crest-like body roughly 50 nm thick. The axoneme is of the 9 + “1” Trepaxonemata pattern. It is surrounded by a periaxonemal sheath of electron-dense material. The cytoplasm is electron lucent and divided into compartments by intracytoplasmic walls of electron-dense material in regions III and IV. The nucleus is an electron-dense cord 60–90 nm thick coiled in a spiral around the axoneme. It reaches the posterior extremity of the gamete where the axoneme is disorganized and is accompanied on all its posterior length by the nucleus. To our knowledge, such a posterior extremity has never been described before in a cyclophyllidean cestode.     

Ultrastructure of spermiogenesis and mature spermatozoon of Breviscolex orientalis (Cestoda: Caryophyllidea)

Spermiogenesis and spermatozoon ultrastructure of the caryophyllidean cestode Breviscolex orientalis Kulakovskaya, 1962, first member of the family Capingentidae studied, a parasite of cyprinid fish Abbottina rivularis, are described using transmission electron microscopy. Spermiogenesis in B. orientalis follows the Type II pattern described by Ba and Marchand (Mém Mus Natl Hist Nat 166:87–95, 1995) for cestodes. It begins with the formation of a zone of differentiation containing a large nucleus and a pair of centrioles. The centrioles are separated from one another by an intercentriolar body composed of three electron-dense layers. Each centriole is associated with typical striated roots. At the beginning of the spermiogenesis, an electron-dense material is observed in the apical region of the differentiation zone. During the initial stage of spermiogenesis, one of the centrioles gives rise to a free flagellum, which then rotates and undergoes proximodistal fusion with the cytoplasmic protrusion of the differentiation zone. The mature spermatozoon of B. orientalis corresponds to the Type III pattern described by Levron et al. (Biol Rev 85:523–543, 2010). It is characterized by the absence of mitochondrion and crested body. Five regions of the mature spermatozoon are differentiated. The main ultrastructural characteristics are: one axoneme of 9 + “1” trepaxonematan pattern, cortical microtubules and nucleus. The comparison of the spermiogenesis of B. orientalis with those of the other caryophyllidean species demonstrates some variation within the order relative to the presence and morphology of the intercentriolar body, the presence of slight rotation of the flagellar bud and a complete proximodistal fusion of the free flagellum with a cytoplasmic protrusion.     

Ultrastructure of spermiogenseis and spermatozoa of Taenia parva Baer, 1926 (Cestoda, Cyclophyllidea, Taeniidae), a parasite of the common genet (Genetta genetta)

We studied the ultrastructure of spermiogenesis and of the mature spermatozoon of Taenia parva, an intestinal cestode of the common genet, Genetta genetta. Spermiogenesis in T. parva is characterized by the growth of the axoneme externally to a cytoplasmic extension. After a slight rotation, the free flagellum fuses with the cytoplasmic extension. This pattern corresponds to type III spermiogenesis according to the scheme proposed by Bâ and Marchand. The zone of differentiation lacks both striated roots associated with the centrioles and the intercentriolar body between them. Nevertheless, the flagellar rotation of about 45° is observed in this species. On the other hand, the mature spermatozoon of T. parva, as in other cestodes, is filiform, tapered at both extremities and lacks mitochondria. The presence of a single crest-like body, periaxonemal sheath, and transverse intracytoplasmic walls are also characteristic ultrastructural features. The pattern of spermiogenesis and the ultrastructural organization of the spermatozoon of T. parva are compared with the available data on cyclophyllideans and, in particular, species of the family Taeniidae.