School of Oceanography, Shanghai Jiao Tong University, Shanghai, 200030, China.
State Key Laboratory of Marine Environmental Science, College of Ocean and Earth Sciences, Xiamen University, Xiamen, 361104, China.
BMC Ecol Evol. 2024 May 31;24(1):73. doi: 10.1186/s12862-024-02265-8.
Monitoring mollusk biodiversity is a great challenge due to their large diversity and broad distribution. Environmental DNA (eDNA) technology is increasingly applied for biodiversity monitoring, but relevant studies on marine mollusks are still limited. Although previous studies have developed several pairs of primers for mollusk eDNA analyses, most of them targeted only a small group of mollusks. In this study, seven primers were designed for the mollusk community and validated and compared with eight pairs of published primers to select the best candidates. After in silico test, MollCOI154 and MollCOI255 primers showed non-specific amplification, and same results were also obtained in published primers (COI204, Sepi, and veneroida). Moll12S100, Moll12S195 and Moll16S primers failed to amplify across all genomic DNA from selected mollusk. Except Moll16S, all developed and two published (unionoida and veneroida) primers were successfully amplified on four eDNA samples from Yangtze River estuary. After annotation of the amplified sequences, MollCOI253 showed higher annotation of the amplification results than the other primers. In conclusion, MollCOI253 had better performance in terms of amplification success and specificity, and can provide technical support for eDNA-based research, which will be beneficial for molluscan biodiversity investigation and conservation.
监测软体动物生物多样性是一项巨大的挑战,因为它们具有多样性和广泛的分布。环境 DNA(eDNA)技术越来越多地应用于生物多样性监测,但相关的海洋软体动物研究仍然有限。尽管先前的研究已经为软体动物 eDNA 分析开发了几对引物,但它们大多数仅针对一小部分软体动物。在这项研究中,设计了 7 对用于软体动物群落的引物,并与 8 对已发表的引物进行了验证和比较,以选择最佳候选引物。经过计算机模拟测试,MollCOI154 和 MollCOI255 引物显示出非特异性扩增,而在已发表的引物(COI204、Sepi 和 veneroida)中也得到了相同的结果。Moll12S100、Moll12S195 和 Moll16S 引物未能在所选软体动物的所有基因组 DNA 上扩增。除了 Moll16S 外,所有开发的和 2 对已发表的(unionoida 和 veneroida)引物都成功地在长江口的 4 个 eDNA 样本上扩增。对扩增序列进行注释后,MollCOI253 显示出比其他引物更高的扩增结果注释率。总之,MollCOI253 在扩增成功率和特异性方面表现更好,可为基于 eDNA 的研究提供技术支持,这将有利于软体动物生物多样性调查和保护。