Development of environmental DNA metabarcoding primers for marine mollusks and comparison with published primers.

IF 2.3 Q2 ECOLOGY BMC ecology and evolution Pub Date : 2024-05-31 DOI:10.1186/s12862-024-02265-8
Xiaojing Shi, Yihui Jiang, Ling Cao, Cong Zeng
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Abstract

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.

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为海洋软体动物开发环境 DNA 代谢编码引物并与已发表的引物进行比较。
由于软体动物种类繁多、分布广泛,监测其生物多样性是一项巨大的挑战。环境 DNA(eDNA)技术越来越多地应用于生物多样性监测,但对海洋软体动物的相关研究仍然有限。虽然之前的研究已经开发了几对用于软体动物 eDNA 分析的引物,但大多数引物只针对一小部分软体动物。本研究针对软体动物群落设计了七对引物,并与已发表的八对引物进行了验证和比较,选出了最佳候选引物。经过硅测试,MollCOI154 和 MollCOI255 引物出现了非特异性扩增,已发表引物(COI204、Sepi 和 veneroida)也出现了同样的结果。Moll12S100、Moll12S195 和 Moll16S 引物未能对所选软体动物的所有基因组 DNA 进行扩增。除 Moll16S 引物外,所有已开发的引物和两种已发表的引物(unionoida 和 veneroida)均在长江口的四个 eDNA 样品中成功扩增。对扩增序列进行注释后,MollCOI253 的注释率高于其他引物。总之,MollCOI253引物在扩增成功率和特异性方面表现较好,可为基于eDNA的研究提供技术支持,有利于软体动物生物多样性的调查和保护。
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