Towards harmonization of DNA metabarcoding for monitoring marine macrobenthos: the effect of technical replicates and pooled DNA extractions on species detection

Laure Van den Bulcke, Annelies De Backer, B. Ampe, S. Maes, J. Wittoeck, W. Waegeman, K. Hostens, S. Derycke
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引用次数: 9

Abstract

DNA-based monitoring methods are potentially faster and cheaper compared to traditional morphological benthic identification. DNA metabarcoding involves various methodological choices which can introduce bias leading to a different outcome in biodiversity patterns. Therefore, it is important to harmonize DNA metabarcoding protocols to allow comparison across studies and this requires a good understanding of the effect of methodological choices on diversity estimates. This study investigated the impact of DNA and PCR replicates on the detection of macrobenthos species in locations with high, medium and low diversity. Our results show that two to three DNA replicates were needed in locations with a high and medium diversity to detect at least 80% of the species found in the six DNA replicates, while three to four replicates were needed in the location with low diversity. In contrast to general belief, larger body size or higher abundance of the species in a sample did not increase its detection prevalence among DNA replicates. However, rare species were less consistently detected across all DNA replicates of the location with high diversity compared to locations with less diversity. Our results further show that pooling of DNA replicates did not significantly alter diversity patterns, although a small number of rare species was lost. Finally, our results confirm high variation in species detection between PCR replicates, especially for the detection of rare species. These results contribute to create reliable, time and cost efficient metabarcoding protocols for the characterization of macrobenthos.
用于监测海洋大型底栖动物的DNA代谢编码的协调:技术复制和混合DNA提取对物种检测的影响
与传统的海底形态鉴定相比,基于DNA的监测方法可能更快、更便宜。DNA代谢编码涉及各种方法选择,这些方法可能会引入偏见,导致生物多样性模式的不同结果。因此,协调DNA代谢编码方案以进行研究比较是很重要的,这需要充分了解方法选择对多样性估计的影响。本研究调查了DNA和PCR复制对高、中、低多样性地区大型底栖动物物种检测的影响。我们的结果表明,在具有高和中等多样性的位置需要两到三个DNA复制,以检测在六个DNA复制中发现的至少80%的物种,而在具有低多样性的地方需要三到四个复制。与普遍认为的相反,样本中较大的体型或较高的物种丰度并没有增加其在DNA复制中的检测率。然而,与多样性较低的地点相比,在多样性较高的地点的所有DNA复制中,稀有物种的检测不太一致。我们的研究结果进一步表明,尽管损失了少量稀有物种,但DNA复制的汇集并没有显著改变多样性模式。最后,我们的结果证实了PCR重复之间物种检测的高度变异,特别是对稀有物种的检测。这些结果有助于为大型底栖动物的表征创建可靠、时间和成本高效的元条形码协议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Metabarcoding and Metagenomics
Metabarcoding and Metagenomics Agricultural and Biological Sciences-Animal Science and Zoology
CiteScore
5.40
自引率
0.00%
发文量
25
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