Kostygov A Iu, Malysheva M N, Frolov A O
Parazitologiia. 2011 Nov-Dec;45(6):409-24.
Results of study of Leptomonas nabiculae using various molecular markers and different material (cultures D2 et Nfm2) contradicted each other and taxonomic position of this species. We investigated morphology of the cells in these cultures as well as in hapantotype of L. nabiculae and those of L. peterhoffi and L. occidentalis that had been described from the same host species. We also reconstructed 18S rRNA gene phylogeny using sequences from both cultures. The D2 culture according to its morphology and phylogenetic position revealed to be a Crithidia that had accompanied L. nabiculae in a mixed infection. We named it Crithidia dedva. The cells in the hapantotypes of the three Leptomonas species and those of the Nfm2 culture represent a single species that is a Herpetomonas (H. nabiculae) judging by morphology and molecular phylogeny. We also showed that the sequence of 18S rRNA gene that had been formerly determined represents a chimaera. This had resulted in the wrong position of this species on the phylogenetic tree that had contradicted results of the analysis of 5s rRNA gene.
使用各种分子标记和不同材料(培养物D2和Nfm2)对纳比库拉纤细单鞭滴虫进行研究的结果相互矛盾,且该物种的分类地位也不明确。我们研究了这些培养物以及纳比库拉纤细单鞭滴虫单型标本、彼得霍夫纤细单鞭滴虫和西方纤细单鞭滴虫(均从同一宿主物种中描述)的细胞形态。我们还利用两种培养物的序列重建了18S rRNA基因系统发育树。根据其形态和系统发育位置,培养物D2显示为一种锥虫,它在混合感染中与纳比库拉纤细单鞭滴虫共存。我们将其命名为德德瓦锥虫。根据形态和分子系统发育分析,三种纤细单鞭滴虫单型标本以及Nfm2培养物中的细胞代表一个单一物种,即赫氏鞭毛虫(纳比库拉赫氏鞭毛虫)。我们还表明先前确定的18S rRNA基因序列是一个嵌合体。这导致该物种在系统发育树上的位置错误,与5S rRNA基因分析结果相矛盾。