Zoology Department, College of Science, King Saud University, Saudi Arabia.
Biology Department, Faculty of Science, King Khaled University, Abha P.O. Box 9004, Saudi Arabia.
Saudi J Biol Sci. 2014 Jan;21(1):65-70. doi: 10.1016/j.sjbs.2013.10.001. Epub 2013 Oct 11.
Schistosoma mansoni is mediated through the intermediate host Biomphalaria arabica which lives in Saudi Arabia. Molecular characterization and identification of this intermediate host are important for epidemiological studies of schistosomiasis. The present work aimed to determine the molecular variations among the populations of B. arabica found in Southern part of Saudi Arabia, and to develop species-specific primers for identification of these snails as a first step in the development of multiplex PCR for simultaneously identifying the snails and diagnosing its infections in a single step. Five populations of Saudi B. arabica snails were collected from freshwater bodies. Three populations were collected from Asser and two populations were collected from AL-Baha. Genomic DNA was extracted from snails and was amplified using five different RAPD-PCR primers. The banding patterns of amplified materials by primers P1 and P5 were identical in all populations. However, the rest primers displayed intra-specific differences among populations with variable degrees. Largest sizes of RAPD-PCR products were cloned into TA cloning vector as a preparatory step for DNA sequence analysis. After sequencing, similarity searches of obtained DNA sequences revealed that there are no similar sequences submitted to genebank data bases and its associated banks. The results obtained will be helpful in the development of simultaneous identification of B. arabica snails and diagnosis of S. mansoni infection within it in a single step by an implementation of multiplex PCR.
曼氏血吸虫是通过中间宿主阿拉伯滨螺传播的,而阿拉伯滨螺生活在沙特阿拉伯。这种中间宿主的分子特征和鉴定对于血吸虫病的流行病学研究非常重要。本工作旨在确定沙特阿拉伯南部地区发现的阿拉伯滨螺种群之间的分子变异,并开发用于鉴定这些蜗牛的种特异性引物,作为开发同时鉴定蜗牛并在一步中诊断其感染的多重 PCR 的第一步。从淡水体中采集了五个沙特阿拉伯阿拉伯滨螺种群。三个种群来自 Asser,两个种群来自 AL-Baha。从蜗牛中提取基因组 DNA,并使用五个不同的 RAPD-PCR 引物进行扩增。引物 P1 和 P5 扩增材料的带型在所有种群中都是相同的。然而,其余引物在种群间显示出不同程度的种内差异。RAPD-PCR 产物的最大大小被克隆到 TA 克隆载体中,作为 DNA 序列分析的预备步骤。测序后,获得的 DNA 序列的相似性搜索显示,没有相似的序列提交到基因库数据库及其相关银行。所得结果将有助于通过实施多重 PCR 一步法同时鉴定阿拉伯滨螺并诊断其中的曼氏血吸虫感染。