纤毛幼虫变成带刺的:原子叶虫微缩微囊的新发现(迪亚那亚目:半尾总科)

IF 2.8 2区 生物学 Q1 ZOOLOGY
Peter A. Smirnov,Alexandra N. Ivanova,Anna Gonchar
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引用次数: 0

摘要

摘要背景Miracidia是digenean的幼虫,感染软体动物宿主。在许多物种中,它们是主动定位蜗牛的纤毛游泳者。然而,在一些digenean谱系中,miracidia是小型化的,被动地进入软体动物体内,被吞食。主动miracidia与被动miracidia的区别是明显的,后者通常是简化的,并且具有形态上的新颖性。在Hemiurata组中,miracidia显示出减少的纤毛,并进化出表面刺。一个极端的例子是原子叶植物的微小藻,它的整个身体被刺覆盖。幼虫纤毛被认为是Neodermata的关键特征之一,但它在原基因B. progenetica中却缺失了。这样的转变是如何发生的?结果通过连续透射电镜观察,我们发现原芽孢杆菌的微囊被3个带刺的上皮板覆盖。每根脊柱由细长的细胞内结构支撑,类似于纤毛的条纹根。与非小型化的微型微生物相比,微型微生物的所有器官系统都明显缩小。对蜗牛寄主的实验感染表明,微生物在变态时脱落其上皮板并转化为孢子囊,孢子囊迁移到蜗牛心脏。孢子囊表面由新生皮特有的膜质通道外翻而出。除了体壁的这种转变外,变态涉及很少的结构变化。在最初的两周内,母孢子囊的大小增加了三倍,肌肉细胞和新生皮层细胞的数量增加,可能是通过干细胞分裂和分化。蜗牛血细胞似乎对感染有反应并与孢子囊接触,形成短的细胞外桥。结论:微型化伴随着感染策略的转变,推动了miracidia结构新颖性的出现。在原芽孢杆菌中,棘取代了表面纤毛,利用纤毛条纹根作为结构支架。虽然与非小型化的微型微生物相比,原遗传双歧杆菌的微型微生物大大简化,但其母孢子囊恢复了体细胞的复杂性,并发育成与其他微型微生物相当的蠕虫。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ciliated larvae turn spiny: novelties in the miniaturized miracidium of Bunocotyle progenetica (Digenea: Hemiuroidea)
Abstract Background Miracidia, the larvae of digeneans, infect a molluscan host. In many species they are ciliated swimmers that actively locate a snail. In several digenean lineages, however, the miracidia are miniaturized and enter molluscs passively, being swallowed. The contrast between active and passive miracidia is sharp, and the latter are typically simplified and feature morphological novelties. In the Hemiurata group, miracidia show reduced ciliation and have evolved surface spines. An extreme example is the miracidium of Bunocotyle progenetica , whose entire body is covered with spines. Larval ciliation is considered one of the key features of Neodermata, yet it is lost in B. progenetica . How could such a transformation have occurred? Results Using serial transmission electron microscopy, we show that the miracidium of B. progenetica is covered by three spiny epithelial plates. Each spine is supported by an elongated intracellular structure similar to the striated rootlet of a cilium. All organ systems of the miracidium are markedly reduced relative to those of non-miniaturized miracidia. Experimental infection of the snail host revealed that the miracidium sheds its epithelial plates upon metamorphosis and transforms into a sporocyst, which migrates to the snail heart. The sporocyst surface arises through eversion of the peculiar membranous channels of the neodermis. Apart from this transformation of the body wall, metamorphosis involves few structural changes. Over the first two weeks, the mother sporocyst triples in size, increasing the number of muscle cells and neodermis cytons, likely through stem-cell division and differentiation. Snail haemocytes appear to respond to the infection and contact the sporocyst, forming short extracellular bridges. Conclusions Miniaturization accompanied by a shift in infection strategy has driven the emergence of structural novelties in miracidia. In B. progenetica , spines have replaced surface cilia, co-opting the ciliary striated rootlet as a structural scaffold. Although the miracidium of B. progenetica is greatly simplified relative to non-miniaturized miracidia, its mother sporocyst restores somatic complexity and develops into worms comparable to those of other digeneans.
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来源期刊
CiteScore
4.90
自引率
0.00%
发文量
29
审稿时长
>12 weeks
期刊介绍: Frontiers in Zoology is an open access, peer-reviewed online journal publishing high quality research articles and reviews on all aspects of animal life. As a biological discipline, zoology has one of the longest histories. Today it occasionally appears as though, due to the rapid expansion of life sciences, zoology has been replaced by more or less independent sub-disciplines amongst which exchange is often sparse. However, the recent advance of molecular methodology into "classical" fields of biology, and the development of theories that can explain phenomena on different levels of organisation, has led to a re-integration of zoological disciplines promoting a broader than usual approach to zoological questions. Zoology has re-emerged as an integrative discipline encompassing the most diverse aspects of animal life, from the level of the gene to the level of the ecosystem. Frontiers in Zoology is the first open access journal focusing on zoology as a whole. It aims to represent and re-unite the various disciplines that look at animal life from different perspectives and at providing the basis for a comprehensive understanding of zoological phenomena on all levels of analysis. Frontiers in Zoology provides a unique opportunity to publish high quality research and reviews on zoological issues that will be internationally accessible to any reader at no cost. The journal was initiated and is supported by the Deutsche Zoologische Gesellschaft, one of the largest national zoological societies with more than a century-long tradition in promoting high-level zoological research.
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