Hall K A, Cribb T H, Barker S C
Department of Parasitology, University of Queensland, Brisbane, Australia.
Syst Parasitol. 1999 Jun;43(2):81-92. doi: 10.1023/a:1006113721899.
There is no morphological synapomorphy for the disparate digeneans, the Fellodistomidae Nicoll, 1909. Although all known life-cycles of the group include bivalves as first intermediate hosts, there is no convincing morphological synapomorphy that can be used to unite the group. Sequences from the V4 region of small subunit (18S) rRNA genes were used to infer phylogenetic relationships among 13 species of Fellodistomidae from four subfamilies and eight species from seven other digenean families: Bivesiculidae; Brachylaimidae; Bucephalidae; Gorgoderidae; Gymnophallidae; Opecoelidae; and Zoogonidae. Outgroup comparison was made initially with an aspidogastrean. Various species from the other digenean families were used as outgroups in subsequent analyses. Three methods of analysis indicated polyphyly of the Fellodistomidae and at least two independent radiations of the subfamilies, such that they were more closely associated with other digeneans than to each other. The Tandanicolinae was monophyletic (100% bootstrap support) and was weakly associated with the Gymnophallidae (< 50-55% bootstrap support). Monophyly of the Baccigerinae was supported with 78-87% bootstrap support, and monophyly of the Zoogonidae + Baccigerinae received 77-86% support. The remaining fellodistomid species, Fellodistomum fellis, F. agnotum and Coomera brayi (Fellodistominae) plus Proctoeces maculatus and Complexobursa sp. (Proctoecinae), formed a separate clade with 74-92% bootstrap support. On the basis of molecular, morphological and life-cycle evidence, the subfamilies Baccigerinae and Tandanicolinae are removed from the Fellodistomidae and promoted to familial status. The Baccigerinae is promoted under the senior synonym Faustulidae Poche, 1926, and the Echinobrevicecinae Dronen, Blend & McEachran, 1994 is synonymised with the Faustulidae. Consequently, species that were formerly in the Fellodistomidae are now distributed in three families: Felldistomidae; Faustulidae (syn. Baccigerinae Yamaguti, 1954); and Tandanicolidae Johnston, 1927. We infer that the use of bivalves as intermediate hosts by this broad range of families indicates multiple host-switching events within the radiation of the Digenea.
对于分类各异的复殖吸虫——1909年尼科尔建立的费氏吸虫科而言,不存在形态学上的共衍征。尽管该类群所有已知的生活史都包括双壳类作为第一中间宿主,但没有令人信服的形态学共衍征可用于将该类群统一起来。利用小亚基(18S)核糖体RNA基因V4区域的序列来推断来自四个亚科的13种费氏吸虫科吸虫以及来自其他七个复殖吸虫科的8个物种之间的系统发育关系:双囊吸虫科;短咽吸虫科;牛首吸虫科;戈尔戈德吸虫科;裸茎吸虫科;孔肠吸虫科;和后睾吸虫科。最初以外肛吸虫作为外类群进行比较。在随后的分析中,来自其他复殖吸虫科的各种物种被用作外类群。三种分析方法均表明费氏吸虫科是多系的,且亚科至少有两次独立的辐射演化,因此它们与其他复殖吸虫的关系比它们彼此之间的关系更为密切。坦氏吸虫亚科是单系的(自展支持率为100%),并且与裸茎吸虫科的关系较弱(自展支持率<50 - 55%)。巴氏吸虫亚科的单系性得到了78 - 87%的自展支持,后睾吸虫科 + 巴氏吸虫亚科的单系性得到了77 - 86%的支持。其余的费氏吸虫物种,费氏费洛吸虫、费氏无名吸虫和布雷氏库梅拉吸虫(费氏吸虫亚科)加上黄斑前殖吸虫和复杂囊吸虫属(前殖吸虫亚科),形成了一个单独的分支,自展支持率为74 - 92%。基于分子、形态学和生活史证据,将巴氏吸虫亚科和坦氏吸虫亚科从费氏吸虫科中移出,并提升为科级地位。巴氏吸虫亚科在1926年波切建立的高级同物异名福氏吸虫科下提升,1994年德龙恩、布伦德和麦克伊克兰建立的棘短颈吸虫亚科与福氏吸虫科同义。因此,以前属于费氏吸虫科的物种现在分布在三个科中:费氏吸虫科;福氏吸虫科(同义名:1954年山口建立的巴氏吸虫亚科);和1927年约翰斯顿建立的松果吸虫科。我们推断,如此广泛的科都以双壳类作为中间宿主,这表明在复殖吸虫的辐射演化过程中发生了多次宿主转换事件。