Ct. Ba et B. Marchand, ULTRASTRUCTURE OF SPERMIOGENESIS AND THE SPERMATOZOON OF VAMPIROLEPIS-MICROSTOMA (CESTODA, HYMENOLEPIDIDAE), INTESTINAL PARASITE OF RATTUS-RATTUS, Microscopy research and technique, 42(3), 1998, pp. 218-225
Spermiogenesis in Vampirolepis micrastoma begins with the formation of
a nuclear cone and a differentiation zone. This is delimited at the f
ront by arched membranes, bordered by cortical microtubules, and conta
ins two parallel centrioles linked together at their bases by electron
-dense, amorphous material. The nuclear cone elongates, becomes filifo
rm, and migrates into the spermatid body. Later, one of the centrioles
gives rise to a flagellum that grows at the same pace as the cortical
microtubules. Subsequently, 6 crested bodies form and the old spermat
id separates from the residual cytoplasm, The mature V. microstoma spe
rmatozoon is filiform and lacks mitochondria. Its anterior end exhibit
s six crested bodies 100 to 200 nm thick of unequal lengths. The axone
me is of the 9+''1'' pattern. The cortical microtubules are spiralized
and make an angle of about 20 to 30 degrees to the spermatozoon axis,
except at their posterior extremity where they become parallel to thi
s axis. The nucleus is an electron-dense cord coiled in a spiral aroun
d the axoneme. The cytoplasm is slightly dense but contains many elect
ron-dense granules in regions III, IV, and V of the spermatozoon. The
presence of centrioles linked together at their bases by electron-dens
e material has never, to our knowledge, been reported in a Platyhelmin
th. Likewise, a nuclear migration, right from the beginning to the end
of spermiogenesis, has never been described in a cestode. In addition
, we observe fur the first time the existence of six crested bodies in
a cestode from a Mammal. Microsc. Res. Tech. 42:218-225, 1998. (C) 19
98 Wiley-Liss, Inc.