State Key Laboratory of Veterinary Etiological Biology, Lanzhou Veterinary Research Institute of Chinese Academy of Agricultural Science, Gansu, PR China.
Acta Trop. 2012 Oct;124(1):92-7. doi: 10.1016/j.actatropica.2012.07.001. Epub 2012 Jul 14.
Due to the difficulty in morphological identification the development of reliable molecular tools for species distinction is a priority for piroplasma. Previous studies based on 18S rRNA and other gene sequences provided a backbone for the phylogeny of piroplasma. However, it is difficult to discriminate species in a comprehensive sample. Here, the abilities of eight DNA regions including 18S rRNA, 28S rRNA, internal transcribed spacer (ITS) regions and COI genes, have been compared as candidates of DNA barcodes for piroplasma. In total, 484 sequences of piroplasma were collected from this study and GenBank. The eight proposed DNA regions were evaluated according to the criterion of Consortium for the Barcode of Life (CBOL). From this evaluation, ITS2 had 100% PCR amplification efficiency, an ideal sequence length, the largest gap between the intra- and inter-specific divergence, 98% identification efficiency at the genus level, and 92% at the species level. Thus, we propose that ITS2 is the most ideal DNA barcode based on the current database for piroplasma.
由于形态学鉴定困难,开发可靠的分子工具来区分种属是梨形虫学的当务之急。先前基于 18S rRNA 和其他基因序列的研究为梨形虫的系统发育提供了基础。然而,在综合样本中很难区分物种。在这里,比较了包括 18S rRNA、28S rRNA、内部转录间隔区(ITS)区域和 COI 基因在内的 8 个 DNA 区域的能力,作为梨形虫 DNA 条形码的候选者。本研究共从 GenBank 收集了 484 个梨形虫序列。根据生命条形码联盟(CBOL)的标准,对这 8 个提议的 DNA 区域进行了评估。从这个评估中,ITS2 具有 100%的 PCR 扩增效率、理想的序列长度、种内和种间差异最大的间隙、98%的属水平鉴定效率和 92%的种水平鉴定效率。因此,我们建议基于当前的梨形虫数据库,ITS2 是最理想的 DNA 条形码。