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Evolutionary anatomy of the muscular apparatus involved in the anchoring of Acanthocephala to the intestinal wall of their vertebrate hosts

机译:肌肉菌锚杆锚固锚杆锚定腹部脑壁的进化解剖学

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Different conceptions exist regarding structure, function, and evolution of the muscles that move the acanthocephalan presoma, including the proboscis, i.e., the usually hooked hold-fast anchoring these endoparasites to the intestinal wall of their vertebrate definitive hosts. In order to clarify the unresolved issues, we carried out a light microscopic analysis of series of semi-thin sections and whole mounts representing the three traditional acanthocephalan classes: Archiacanthocephala (Macracanthorhynchus hirudinaceus), Eoacanthocephala (Paratenuisentis ambiguus, Tenuisentis niloticus), and Palaeacanthocephala (Acanthocephalus anguillae, Echinorhynchus truttae, Pomphorhynchus laevis, Corynosoma sp.). Combining our data with published light, transmission electron, and scanning electron microscopic data, we demonstrate that receptacle protrusor and proboscis receptacle in Archi- and Eoacanthocephala are homologous to the outer and inner wall of the proboscis receptacle in Palaeacanthocephala. Besides the proboscis receptacle and a "surrounding muscle," the last common ancestor of Acanthocephala presumably possessed a proboscis retractor, receptacle retractor, neck retractor (continuous with lemnisci compressors), and retinacula. These muscles most probably evolved in the acanthocephalan stem line. Moreover, the last common ancestor of Acanthocephala presumably possessed only a single layer of muscular cords under the presomal tegument while the metasomal body wall had circular and longitudinal strands. Two lateral receptacle flexors (also lateral receptacle protrusors), an apical muscle plate (surrounding one or two apical sensory organs), a midventral longitudinal muscle, and the differentiation of longitudinal body wall musculature at the base of the proboscis probably emerged within Archiacanthocephala. All muscles have a common organization principle: a peripheral layer of contractile filaments encloses the cytoplasm.
机译:关于移动棘头前肿瘤的肌肉的结构、功能和进化存在不同的概念,包括喙,即通常钩状的支架,将这些内寄生虫牢牢固定在脊椎动物最终宿主的肠壁上。为了澄清尚未解决的问题,我们对代表三个传统棘头类的一系列半薄切片和整体坐骑进行了光镜分析:无棘头类(Macracanthorhynchus hirudinaceus)、无棘头类(Paratenuisentis ambiguus、Tenuisentis niloticus),和狭棘头类(棘头类、棘喙类、金鸡鱼、棒状体)。将我们的数据与已发表的光镜、透射电子显微镜和扫描电子显微镜数据相结合,我们证明了Archi-和Eocanthocephala中的前喙插座和长鼻插座与Palaecanthocephala中的长鼻插座的外壁和内壁同源。除了长鼻托和“周围肌肉”,棘头类的最后一个共同祖先可能还拥有一个长鼻牵开器、托牵开器、颈部牵开器(与lemnisci压缩器相连)和支持带。这些肌肉很可能是在棘头脑干系中进化而来的。此外,棘头类的最后一个共同祖先可能在体前被盖下只有一层肌索,而质体体体壁有圆形和纵向股。两个外侧插座屈肌(也就是外侧插座前伸肌)、一个顶端肌板(围绕一个或两个顶端感觉器官)、一个中腹侧纵肌,以及喙基部的纵向体壁肌肉组织的分化可能出现在Archiacanthocephala内。所有的肌肉都有一个共同的组织原理:细胞质周围有一层可收缩的细丝。

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