Lawton Scott P, Lim Rivka M, Dukes Juliet P, Kett Stephen M, Cook Richard T, Walker Anthony J, Kirk Ruth S
Molecular Parasitology Laboratory, School of Life Sciences, Kingston University, Kingston upon Thames, Surrey KT1 2EE, UK.
Molecular Parasitology Laboratory, School of Life Sciences, Kingston University, Kingston upon Thames, Surrey KT1 2EE, UK.
Infect Genet Evol. 2015 Oct;35:63-74. doi: 10.1016/j.meegid.2015.07.021. Epub 2015 Jul 18.
Radix spp. are intermediate host snails for digenean parasites of medical and veterinary importance. Within this genus, species differentiation using shell and internal organ morphology can result in erroneous species identification, causing problems when trying to understand the population biology of Radix. In the present study, DNA barcoding, using cox1 and ITS2 sequences, identified populations of Radix auricularia and Radix balthica from specimens originally morphologically identified as Radix peregra from the UK. Assessment of cox1 and ITS2 as species identification markers showed that, although both markers differentiated species, cox1 possessed greater molecular diversity and higher phylogenetic resolution. Cox1 also proved useful for gaining insights into the evolutionary relationships of Radix species populations. Phylogenetic analysis and haplotype networks of cox1 indicated that R. auricularia appeared to have invaded the UK several times; some haplotypes forming a distinct UK specific clade, whilst others are more akin to those found on mainland Europe. This was in contrast to relationships between R. balthica populations, which had low molecular diversity and no distinct UK specific haplotypes, suggesting recent and multiple invasions from mainland Europe. Molecular techniques therefore appear to be crucial for distinguishing Radix spp., particularly using cox1. This barcoding marker also enables the population biology of Radix spp. to be explored, and is invaluable for monitoring the epidemiology of fluke diseases especially in the light of emerging diseases and food security.
萝卜螺属的螺类是具有医学和兽医学重要性的复殖吸虫寄生虫的中间宿主。在该属内,利用贝壳和内部器官形态进行物种区分可能会导致错误的物种鉴定,在试图了解萝卜螺种群生物学时会引发问题。在本研究中,利用细胞色素氧化酶亚基I(cox1)和核糖体DNA内转录间隔区2(ITS2)序列进行DNA条形码分析,从最初在形态上被鉴定为来自英国的截口土蜗的标本中识别出了耳萝卜螺和椭圆萝卜螺的种群。对cox1和ITS2作为物种鉴定标记的评估表明,尽管这两个标记都能区分物种,但cox1具有更大的分子多样性和更高的系统发育分辨率。Cox1还被证明有助于深入了解萝卜螺物种种群的进化关系。cox1的系统发育分析和单倍型网络表明,耳萝卜螺似乎多次入侵英国;一些单倍型形成了一个独特的英国特有分支,而其他单倍型则更类似于在欧洲大陆发现的单倍型。这与椭圆萝卜螺种群之间的关系形成对比,椭圆萝卜螺种群的分子多样性较低,没有独特的英国特有单倍型,表明近期有多次从欧洲大陆的入侵。因此,分子技术对于区分萝卜螺属的物种似乎至关重要,特别是使用cox1。这种条形码标记还能够探索萝卜螺属物种的种群生物学,对于监测吸虫病的流行病学尤其具有重要价值,特别是鉴于新出现的疾病和食品安全问题。