[以srivastavai Schistotaenia srivastavai Schistotaenia srivastavai Raush, 1970]。

Parazitologiia Pub Date : 2014-05-01
K V Regel', N A Pospekhova
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引用次数: 0

摘要

本文研究了鄂霍次克-科雷马地区红颈灰背虫(Podiceps griseigena)中较为罕见的寄生虫斯里瓦斯塔瓦血吸虫(Schistotaenia srivastavai)和中间寄主豆蝇和蜻蜓幼虫的真尾绦虫(真尾绦虫或真尾囊虫)形态发生。用自然感染的蜻蜓幼虫的材料重建了胚胎后发育阶段,这与Mrazek(1927)和Rees(1973)研究的Tatria s.l.属的metacestodes发育的已发表数据相对应。荚膜囊虫是血吸虫科中分布最广的一种形态变异的囊囊虫。根据Gulyaev(1989)和我们的数据,该科的物种(Mircia属)也有子囊绦虫或多尾绦虫的多头修饰。它代表了一个母体个体,在胚胎后发育过程中充满了许多小的子代囊虫。这些囊尾蚴是由外壁的单个芽形成的;后来,它们在母体的初级腔中受精。因此,每个子代个体都有自己的单层囊,与其他尾尾蚴的双层囊的内层同源。据推测,单头尾尾蚴囊囊的外层与多尾蚴母体个体的外壁是同源的。最后,尾尾蚴第三种变异的诊断特征,即巨尾尾蚴(meggalocercus),与Boertje(1975)研究的尾尾蚴(Schistotaenia tenuicirus)的特征相对应。在整个内囊表面形成螺旋结构(在D. asper中,仅在其背面),并且在幼虫的孢子中有少量的先头虫(D. asper具有多节段的孢子),这与D. asper的不同之处在于。其原因,为什么如此大的保护膜(外囊和内囊)发展相对较小的预期体,尚不清楚。因此,血吸虫科的生命周期代表了尾尾绦虫的所有三种变体:真尾尾绦虫(Shistotaenia, Tatria, Ryjikovilepis, Joyeuxilepis),多尾绦虫(Mircia属)和巨尾绦虫(S. tenuicirus)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[On morphogenesis of metacestodes from the family Schistotaeniidae (Cyclophyllidea) by the example of euascocercus Schistotaenia srivastavai Raush, 1970].

Morphogenesis of the true ascocercus (euascocercus or euascocysticercoid) was studied in Schistotaenia srivastavai, a relatively rare parasite of the Red-necked Grebe Podiceps griseigena, and of intermediate hosts, damselfy and dragonfly larvae, in the Okhotsk-Kolyma region. Stages of postembryonic development were reconstructed by the material from spontaneously infected dragonflies' larvae, which corresponded to the published data on the development of metacestodes from the genus Tatria s. l. studied by Mrazek (1927) and Rees (1973). The euascocercus is the most widespread morphological modification of ascocysticercoids among Schistotaeniidae. According to Gulyaev (1989) and our data, the species of the family (the genus Mircia) have also a polycephalic modification of the ascocercus, or the multicercus. It represents a maternal individual that is filled with numerous small filial cysticercoids during the postembryonic development. These cysticercoids are formed of individual buds in the outer wall; later on, they are gemmated into the primary cavity of the maternal individual. Consequently, each daughter individual possesses its own single-layer exocyst, homological to the inner layer of the two-layered exocyst of the other ascocerci. Supposedly, exocyst's outer layer of monocephalic ascocerci is homologous to the outer wall of multicercus' maternal individual. Finally, diagnostic features of the third modification of ascocerci, namely megalocercus, described in the uniquely large metacestode Dioecocestus asper, corresponds to the characteristic of the metacestode Schistotaenia tenuicirrus, studied by Boertje (1975). S. tenuicirrus differs from D. asper in the spiral configuration formed on the entire surface of the endocyst (in D. asper, only on its dorsal side), and in a low number of proglottids in the larval strobile (D. asper possesses a multisegmental strobile). The reason, why so large protective envelopes (exo- and endocysts) develop in S. tenuicirrus with relatively small size of prospective body, remains unclear. Thus, life cycles of Schistotaeniidae represent all three modifications of the ascocerci: the true ascocercus (Shistotaenia, Tatria, Ryjikovilepis, Joyeuxilepis), the multicercus (genus Mircia), and the megalocercus (S. tenuicirrus).

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