2010
DOI: 10.1007/s00436-010-2125-2
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Ultrastructure of the spermatozoon of Taeniarhynchus saginatus (syn. Taenia saginata) (Goeze, 1782) Weinland, 1858 (Cestoda, Taeniidae) an intestinal parasite of human

Abstract: 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 re… Show more

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Cited by 5 publications
(3 citation statements)
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“…In the Cyclophyllidea, the simultaneous presence of a periaxonemal sheath and intracytoplasmic walls is usually linked with the absence of dense granules (Justine 1998) as also observed in other paruterinids (Yoneva et al 2009(Yoneva et al , 2010. Besides the paruterinids, mutual exclusion between these characters, in agreement with Justine (1998), is also reported for the taeniids and metadilepidids, as well as davaineids and inermicapsiferine anoplocephalids (Featherston 1971;Bâ and Marchand 1994a, b, c;Miquel et al 2000Miquel et al , 2009aMiquel et al , 2010Ndiaye et al 2003a;Willms et al 2003Willms et al , 2004Bâ et al 2005aBâ et al , b, 2011Yoneva et al 2006).…”
Section: Discussionsupporting
confidence: 61%
“…In the Cyclophyllidea, the simultaneous presence of a periaxonemal sheath and intracytoplasmic walls is usually linked with the absence of dense granules (Justine 1998) as also observed in other paruterinids (Yoneva et al 2009(Yoneva et al , 2010. Besides the paruterinids, mutual exclusion between these characters, in agreement with Justine (1998), is also reported for the taeniids and metadilepidids, as well as davaineids and inermicapsiferine anoplocephalids (Featherston 1971;Bâ and Marchand 1994a, b, c;Miquel et al 2000Miquel et al , 2009aMiquel et al , 2010Ndiaye et al 2003a;Willms et al 2003Willms et al , 2004Bâ et al 2005aBâ et al , b, 2011Yoneva et al 2006).…”
Section: Discussionsupporting
confidence: 61%
“…Thus, sperm cells with two axonemes are present in the orders Diphyllobothriidea, Spathebothriidea, Haplobothriidea, Onchoproteocephalidea, and Trypanorhyncha [21][22][23][46][47][48][49][50][51][52][53][54][55][56][57][58][59][60]. Contrarily, spermatozoa with one axoneme are present in the orders Caryophyllidea, Cyclophyllidea, Lecanicephalidea, Nippotaeniidea, Phyllobothriidea, and Tetrabothiidea [21][22][23][26][27][28][29][30][31][32][61][62][63][64][65][66][67][68][69][70][71][72]. In the order Diphyllidea, there are some discrepancies between the spermiogenesis process and the resulting spermatozoa.…”
Section: Spermatozoonmentioning
confidence: 99%
“…In the Cestoda, there are numerous ultrastructural studies describing spermiogenesis and/or the spermatozoon, particularly in the order Cyclophyllidea [ 23 , 26 , 27 , 28 , 29 , 30 , 31 , 32 ]. However, in the Catenotaeniidae family, ultrastructural aspects of spermiogenesis and/or the spermatozoon have only been studied in two species, namely Catenotaenia pusilla (Goeze, 1782) (Catenotaeniinae Spassky, 1950) and Skrjabinotaenia lobata (Baer, 1925) (Skrjabinotaeniinae) [ 33 , 34 ].…”
Section: Introductionmentioning
confidence: 99%