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首页> 外文期刊>Parasitology Research >Molecular differentiation of five Sarcocystis species in sika deer (Cervus nippon centralis) in Japan based on mitochondrial cytochrome c oxidase subunit I gene (cox1) sequences
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Molecular differentiation of five Sarcocystis species in sika deer (Cervus nippon centralis) in Japan based on mitochondrial cytochrome c oxidase subunit I gene (cox1) sequences

机译:基于线粒体细胞色素C氧化酶亚基I基因(COX1)序列的日本锡卡鹿(Cervus Nippon Centrisis)中五种Sarcocystis种类的分子分化

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Several surveys of Sarcocystis infection in sika deer in Japan have shown a high prevalence, but the identification has been unclear because molecular data have been lacking or have been limited to 18S ribosomal RNA gene sequences. Thus, in our previous study based on such sequences, some Sarcocystis isolates from sika deer were not clearly separated from other species in the phylogenetic analysis. In the present study, we therefore characterized sarcocyst isolates from sika deer (Cervus nippon centralis) at the mitochondrial cytochrome c oxidase subunit I gene (cox1). Moreover, we developed a multiplex PCR based on cox1 sequences of all species found, so that we could rapidly identify sarcocysts of these species. Twenty-one sarcocysts from nine sika deer were examined. Five distinct cox1 sequence types, each with a high sequence identity (>99%), were found, and the sarcocysts could thus be classified into five species. Based on the sequence comparisons and the phylogeny, Sarcocystis spp. of types 1, 3, and 5 are considered to represent three new species, which were most closely related to Sarcocystis silva/Sarcocystis truncata, Sarcocystis entzerothi, and Sarcocystis iberica/Sarcocystis venatoria, respectively. There was a slight uncertainly whether Sarcocystis sp. with type 2 sequences represented a new species or was identical to Sarcocystis tarandi. Type 4 sequences showed 99% identity with those of Sarcocystis pilosa from sika deer in Lithuania and have therefore been assigned to this species. In the multiplex PCR, type-specific fragments were successfully amplified for all five Sarcocystis spp., indicating that this assay may be useful for a rapid identification of sarcocysts of these species.
机译:日本锡卡鹿的Sarcocystis感染的几次调查显示出高普遍性,但鉴定尚不清楚,因为分子数据缺乏或限制为18s核糖体RNA基因序列。因此,在我们以前的基于此类序列的研究中,来自Sika鹿的一些Sarcocystis分离物没有明显与系统发育分析中的其他物种分离。因此,在本研究中,我们在线粒体细胞色素C氧化酶亚基I基因(COX1)中的SARCOCYST分离株此外,我们开发了基于发现所有物种的COX1序列的多重PCR,因此我们可以迅速识别这些物种的Sarcocysts。检查了来自九个锡卡鹿的二十一只Sarcocysts。发现五种不同的COX1序列类型,每种序列类型具有高序列同一性(> 99%),因此可以将Sarcocysts分为五种物种。基于序列比较和系统发育,SARCOCYSTIS SPP。在1,3和5型分别被认为是三种新物种,它们分别与Sarcocystis Silva / Sarcocystis truncata,Sarcocystis Exertothi和Sarcocystis Iberica / Sarcococystis Venatoria最密切相关。无论sarcocystis sp是否有略微不确定。 2型序列表示新物种或与Sarcocystis Tarandi相同。 4型序列显示出99%的同一性与立陶宛Sika鹿的Sarcocystis pilosa的身份,因此已被分配给该物种。在多重PCR中,针对所有五个Sarcocystis SPP成功扩增特异性碎片。,表明该测定可用于快速鉴定这些物种的Sarcocysts。

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