Park Joong-Ki, Kim Kyu-Heon, Kang Seokha, Kim Won, Eom Keeseon S, Littlewood D T J
Department of Parasitology, College of Medicine, Chungbuk National University, Cheongju, Chungbuk 361-763, Republic of Korea.
BMC Evol Biol. 2007 Feb 2;7:11. doi: 10.1186/1471-2148-7-11.
The parasitic Platyhelminthes (Neodermata) contains three parasitic groups of flatworms, each having a unique morphology, and life style: Monogenea (primarily ectoparasitic), Trematoda (endoparasitic flukes), and Cestoda (endoparasitic tapeworms). The evolutionary origin of complex life cyles (multiple obligate hosts, as found in Trematoda and Cestoda) and of endo-/ecto-parasitism in these groups is still under debate and these questions can be resolved, only if the phylogenetic position of the Monogenea within the Neodermata clade is correctly estimated.
To test the interrelationships of the major parasitic flatworm groups, we estimated the phylogeny of the Neodermata using complete available mitochondrial genome sequences and a newly characterized sequence of a polyopisthocotylean monogenean Microcotyle sebastis. Comparisons of inferred amino acid sequences and gene arrangement patterns with other published flatworm mtDNAs indicate Monogenea are sister group to a clade of Trematoda+Cestoda.
Results confirm that vertebrates were the first host for stem group neodermatans and that the addition of a second, invertebrate, host was a single event occurring in the Trematoda+Cestoda lineage. In other words, the move from direct life cycles with one host to complex life cycles with multiple hosts was a single evolutionary event. In association with the evolution of life cycle patterns, our result supports the hypothesis that the most recent common ancestor of the Neodermata giving rise to the Monogenea adopted vertebrate ectoparasitism as its initial life cycle pattern and that the intermediate hosts of the Trematoda (molluscs) and Cestoda (crustaceans) were subsequently added into the endoparasitic life cycles of the Trematoda+Cestoda clade after the common ancestor of these branched off from the monogenean lineage. Complex life cycles, involving one or more intermediate hosts, arose through the addition of intermediate hosts and not the addition of a vertebrate definitive host. Additional evidence is required from monopisthocotylean monogeneans in order to confirm the monophyly of the group.
寄生扁形动物(新皮动物门)包含三个寄生性扁虫类群,每个类群都有独特的形态和生活方式:单殖吸虫纲(主要为外寄生)、吸虫纲(内寄生吸虫)和绦虫纲(内寄生绦虫)。这些类群中复杂生命周期(如吸虫纲和绦虫纲中发现的多个专性宿主)以及内/外寄生现象的进化起源仍存在争议,只有正确估计单殖吸虫纲在新皮动物门分支中的系统发育位置,这些问题才能得到解决。
为了测试主要寄生扁虫类群之间的相互关系,我们利用完整的线粒体基因组序列以及一种新鉴定的多后盘单殖吸虫—— Sebastis小杯虫的序列,估计了新皮动物门的系统发育。将推断的氨基酸序列和基因排列模式与其他已发表的扁虫线粒体DNA进行比较,结果表明单殖吸虫纲是吸虫纲 + 绦虫纲分支的姐妹群。
结果证实脊椎动物是新皮动物门主干类群的首个宿主,并且第二个无脊椎动物宿主的加入是吸虫纲 + 绦虫纲分支中发生的单一事件。换句话说,从具有一个宿主的直接生命周期转变为具有多个宿主的复杂生命周期是一个单一的进化事件。结合生命周期模式的进化,我们的结果支持以下假设:产生单殖吸虫纲的新皮动物门的最近共同祖先采用脊椎动物外寄生作为其初始生命周期模式,并且吸虫纲(软体动物)和绦虫纲(甲壳类动物)的中间宿主是在这些类群的共同祖先从单殖吸虫纲分支出来之后,随后被添加到吸虫纲 + 绦虫纲分支的内寄生生命周期中的。涉及一个或多个中间宿主的复杂生命周期是通过添加中间宿主而非脊椎动物终末宿主产生的。需要从单后盘单殖吸虫纲获取更多证据以确认该类群的单系性。