Thaewnon-ngiw Bungorn, Klinbunga Sirawut, Phanwichien Kantimanee, Sangduen Nitsri, Lauhachinda Nitaya, Menasveta Piamsak
Program of Bioscience, Graduate School of Kasetart University, Bangkok 10900, Thailand.
J Biochem Mol Biol. 2004 Jul 31;37(4):493-502. doi: 10.5483/bmbrep.2004.37.4.493.
The genetic diversity and species-diagnostic markers in the introduced apple snail, Pomacea canaliculata and in the native Thai apple snails; Pila ampullacea, P. angelica, P. pesmei, and P. polita, were investigated by restriction analysis of COI and are reported for the first time. Twenty-one composite haplotypes showing non-overlapping distributions among species were found. Genetic heterogeneity analysis indicated significant differences between species (P < 0.0001) and within P. pesmei (P < 0.0001) and P. angelica (P < 0.0004). No such heterogeneity was observed in Pomacea canaliculata (P > 0.0036 as modified by the Bonferroni procedure), P. ampullacea (P = 0.0824-1.000) and P. polita (P = 1.0000). A neighbor-joining tree based on genetic distance between pairs of composite haplotypes differentiated all species and indicated that P. angelica and P. pesmei are closely related phylogenetically. In addition, the 16S rDNA of these species was cloned and sequenced. A species-specific PCR for P. canaliculata was successfully developed with a sensitivity of detection of approximately 50 pg of the target DNA template. The amplification of genomic DNA (50 pg and 25 ng) isolated from the fertilized eggs, and juveniles (1, 7, and 15 d after hatching) of Pomacea canaliculata was also successful, and suggested that Pomacea canaliculata and Pila species can be discriminated from the early stages of development.
通过对细胞色素氧化酶亚基I(COI)进行限制性分析,首次对入侵的福寿螺(Pomacea canaliculata)以及泰国本土苹果螺,即瓶螺(Pila ampullacea)、黄瓶螺(P. angelica)、佩氏瓶螺(P. pesmei)和脉瓶螺(P. polita)的遗传多样性及物种诊断标记进行了研究。发现了21种复合单倍型,它们在不同物种间呈非重叠分布。遗传异质性分析表明,不同物种之间(P < 0.0001)以及佩氏瓶螺(P < 0.0001)和黄瓶螺(P < 0.0004)内部均存在显著差异。在福寿螺(经Bonferroni法校正后P > 0.0036)、瓶螺(P = 0.0824 - 1.000)和脉瓶螺(P = 1.0000)中未观察到这种异质性。基于复合单倍型对之间遗传距离构建的邻接树区分了所有物种,并表明黄瓶螺和佩氏瓶螺在系统发育上密切相关。此外,还对这些物种的16S核糖体DNA进行了克隆和测序。成功开发了一种针对福寿螺的物种特异性聚合酶链反应(PCR),其检测灵敏度约为50 pg目标DNA模板。从福寿螺受精卵以及幼体(孵化后1、7和15天)中分离的基因组DNA(50 pg和25 ng)的扩增也取得成功,这表明福寿螺和瓶螺属物种在发育早期即可区分。