Vidigal T H D A, Magalhães K G, Kissinger J C, Caldeira R L, Simpson A J G, Carvalho O S
Departamento de Zoologia, Instituto de Ciências Biológicas, UFMG, Belo Horizonte, MG, Brasil.
Mem Inst Oswaldo Cruz. 2002;97 Suppl 1:95-7. doi: 10.1590/s0074-02762002000900019.
Due to difficulties concerning morphological identification of planorbid snails of the genus Biomphalaria, and given a high variation of characters and in the organs with muscular tissue, we designed specific polymerase chain reaction (PCR) primers for Brazilian snail hosts of Schistosoma mansoni from available sequences of internal transcribed spacer 2 (ITS2) of the ribosomal RNA gene. From the previous sequencing of the ITS2 region, one primer was designed to anchor in the 5.8S conserved region and three other species-specific primers in the 28S region, flanking the ITS2 region. These four primers were simultaneously used in the same reaction (Multiplex-PCR), under high stringency conditions. Amplification of the ITS2 region of Biomphalaria snails produced distinct profiles (between 280 and 350 bp) for B. glabrata, B. tenagophila and B. straminea. The present study demonstrates that Multiplex-PCR of ITS2-DNAr showed to be a promising auxiliary tool for the morphological identification of Biomphalaria snails, the intermediate hosts of S. mansoni.
由于难以从形态学上鉴定双脐螺属的扁卷螺,且鉴于其特征以及具有肌肉组织的器官存在高度变异性,我们根据曼氏血吸虫巴西螺宿主核糖体RNA基因内部转录间隔区2(ITS2)的可用序列,设计了特异性聚合酶链反应(PCR)引物。根据之前对ITS2区域的测序结果,设计了一个锚定在5.8S保守区域的引物和另外三个位于28S区域、侧翼为ITS2区域的物种特异性引物。这四个引物在高严谨性条件下同时用于同一反应(多重PCR)。双脐螺ITS2区域的扩增产生了光滑双脐螺、嗜气管双脐螺和淡黄双脐螺的不同条带(280至350 bp之间)。本研究表明,ITS2-DNAr的多重PCR是一种很有前景的辅助工具,可用于曼氏血吸虫中间宿主双脐螺的形态学鉴定。