陆生寄生天牛(蛛形纲,原尾目)的综合分子系统发育为了解其变态、入侵水生栖息地和分类的进化过程提供了见解。

IF 3.6 1区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Samuel G.S. Costa , Andrei Tolstikov , Alireza Saboori , Dante Batista-Ribeiro , Javad Noei , Mark S. Harvey , Matthew D. Shaw , Pavel B. Klimov , Zhi-Qiang Zhang , Almir R. Pepato
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引用次数: 0

摘要

寄生螨(绒螨、恙螨和水螨)种类繁多,分布于全球各地,包括 11,000 多个已描述的物种,栖息于陆地、淡水和海洋栖息地。某些种类,如恙螨(Trombiculidae),以脊椎动物宿主和病原体媒介为食,因此在医学和兽医学方面具有重要意义。尽管之前进行了大量研究,但寄生虫分类仍存在争议,尤其是超科和科之间的界限,而缺乏全面的系统发育则加剧了这一争议。大多数寄生藤壶虫的本体发育都有显著的变态现象,寄生幼虫与捕食性的自由生活的脱虫和成虫相比具有异形性。神秘的超科 Allotanaupodoidea 是一个例外,其幼虫和活跃的后幼虫阶段在形态上相似,这表明没有变态可能是一种祖先状态,也可能是一种继发性逆转。此外,关于 Parasitengona 是起源于淡水还是陆地,文献中也存在分歧。在此,我们利用 5 个基因(7838 nt 对齐)推断了 Parasitengona(89 种,36 科)和 307 个外群的系统发生关系。该系统发育表明,Parasitengona起源于陆生,Allotanaoupodoidea次生失去了变态过程。我们复原了超科 Trombidioidea(Trombidioidea sensu lato),它是一个大型的、支持良好的、更高层次的支系,包括 10 个采样科。我们为陆生寄生虫提出了一个新的分类法,即在超科 Trombidioidea 中划分出三个新的主要分支(外科):Trombelloidae(Audyanidae科、Trombellidae科、Neotrombidiidae科、Johnstonianidae科、Chyzeriidae科);Trombidioidae(Microtrombidiidae科、Neothrombiidae科、Achaemenothrombiidae科、Trombidiidae科、Podothrombiidae科);以及Trombiculoidae(=Trombiculidae sensu lato)。将它们加入之前已被确认的超科 Allotanaupodoidea、Amphotrombioidea、Calyptostomatoidea、Erythraeoidea、Tanaupodoidae 和 Yurebilloidae。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A comprehensive molecular phylogeny of the terrestrial Parasitengona (Acariformes, Prostigmata) provides insights into the evolution of their metamorphosis, invasion into aquatic habitats and classification

A comprehensive molecular phylogeny of the terrestrial Parasitengona (Acariformes, Prostigmata) provides insights into the evolution of their metamorphosis, invasion into aquatic habitats and classification

Parasitengona (velvet mites, chiggers and water mites) is a highly diverse and globally distributed mite lineage encompassing over 11,000 described species, inhabiting terrestrial, freshwater and marine habitats. Certain species, such as chiggers (Trombiculidae), have a great medical and veterinary importance as they feed on their vertebrate hosts and vector pathogens. Despite extensive previous research, the classification of Parasitengona is still contentious, particularly regarding the boundaries between superfamilies and families, exacerbated by the absence of a comprehensive phylogeny. The ontogeny of most Parasitengona is distinct by the presence of striking metamorphosis, with parasitic larvae being heteromorphic compared to the predatory free-living deutonymphs and adults. The enigmatic superfamily Allotanaupodoidea is an exception, with larvae and active post-larval stages being morphologically similar, suggesting that the absence of metamorphosis may be either an ancestral state or a secondary reversal. Furthermore, there is disagreement in the literature on whether Parasitengona had freshwater or terrestrial origin. Here, we inferred phylogenetic relationships of Parasitengona (89 species, 36 families) and 307 outgroups using five genes (7,838 nt aligned). This phylogeny suggests a terrestrial origin of Parasitengona and a secondary loss of metamorphosis in Allotanaoupodoidea. We recovered the superfamily Trombidioidea (Trombidioidea sensu lato) as a large, well-supported, higher-level clade including 10 sampled families. We propose a new classification for the terrestrial Parasitengona with three new major divisions (epifamilies) of the superfamily Trombidioidea: Trombelloidae (families Audyanidae, Trombellidae, Neotrombidiidae, Johnstonianidae, Chyzeriidae); Trombidioidae (Microtrombidiidae, Neothrombiidae, Achaemenothrombiidae, Trombidiidae, Podothrombiidae); and Trombiculoidae (=Trombiculidae sensu lato). Adding them to previously recognized superfamilies Allotanaupodoidea, Amphotrombioidea, Calyptostomatoidea, Erythraeoidea, Tanaupodoidae and Yurebilloidae.

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来源期刊
Molecular Phylogenetics and Evolution
Molecular Phylogenetics and Evolution 生物-进化生物学
CiteScore
7.50
自引率
7.30%
发文量
249
审稿时长
7.5 months
期刊介绍: Molecular Phylogenetics and Evolution is dedicated to bringing Darwin''s dream within grasp - to "have fairly true genealogical trees of each great kingdom of Nature." The journal provides a forum for molecular studies that advance our understanding of phylogeny and evolution, further the development of phylogenetically more accurate taxonomic classifications, and ultimately bring a unified classification for all the ramifying lines of life. Phylogeographic studies will be considered for publication if they offer EXCEPTIONAL theoretical or empirical advances.
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