Yamasaki Hiroshi, Izumiyama Shinji, Nozaki Tomoyoshi
Department of Parasitology, National Institute of Infectious Diseases, Ministry of Health, Labour and Welfare, Tokyo 162-8640, Japan.
Department of Parasitology, National Institute of Infectious Diseases, Ministry of Health, Labour and Welfare, Tokyo 162-8640, Japan.
Parasitol Int. 2017 Oct;66(5):573-578. doi: 10.1016/j.parint.2017.06.005. Epub 2017 Jun 22.
We first constructed and characterized the complete mitochondrial genome (mitogenome) sequence of Diphyllobothrium stemmacephalum, the type species of genus Diphyllobothrium, using next generation sequencing (NGS). The mitogenome of D. stemmacephalum was 13,716bp, including 12 protein-coding genes, 22 tRNA genes, 2 rRNA genes and 2 longer intergenic non-coding regions, and has features common to mitogenomes of other cestodes. Although it has been accepted that tRNA for serine (trnS2) in Platyhelminthes lacks a D arm, the trnS2 of D. stemmacephalum was predicted to have a paired D arm as in Diplogonoporus balaenopterae. The non-coding region 2 contained eight tandem repeat units (34nucleotides/unit). This study also corroborated that D. stemmacephalum is phylogenetically more closely related to Dip. balaenopterae than to Diphyllobothrium latum and Diphyllobothrium nihonkaiense. As demonstrated here, mitogenome sequence data obtained using NGS is useful for gaining a better understanding of the systematics, phylogeny and taxonomic revisions involving valuable specimens preserved in museums, universities or research institutes for which sequence data are not yet available, and also for making diagnoses based on clinical samples.
我们首先利用下一代测序(NGS)技术构建并鉴定了阔节裂头绦虫属的模式种——矛头阔节裂头绦虫的完整线粒体基因组(线粒体基因组)序列。矛头阔节裂头绦虫的线粒体基因组为13,716bp,包括12个蛋白质编码基因、22个tRNA基因、2个rRNA基因和2个较长的基因间隔非编码区,具有其他绦虫线粒体基因组的共同特征。虽然普遍认为扁形动物中的丝氨酸tRNA(trnS2)缺乏D臂,但预测矛头阔节裂头绦虫的trnS2具有与须鲸双叶槽绦虫一样的配对D臂。非编码区2包含八个串联重复单元(每个单元34个核苷酸)。本研究还证实,在系统发育上,矛头阔节裂头绦虫与须鲸双叶槽绦虫的关系比与阔节裂头绦虫和日本阔节裂头绦虫更为密切。如此处所示,使用NGS获得的线粒体基因组序列数据有助于更好地理解系统分类学、系统发育以及涉及保存在博物馆、大学或研究机构中尚未有序列数据的珍贵标本的分类学修订,也有助于基于临床样本进行诊断。