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实验室方案对于提高种子 DNA 从地面甲虫反刍物中靶拷贝数与 metabarcoding 读数值之间的相关性非常重要。

Laboratory protocol is important to improve the correlation between target copies and metabarcoding read numbers of seed DNA in ground beetle regurgitates.

机构信息

Applied Animal Ecology Research Unit, Department of Zoology, University of Innsbruck, Technikerstraße 25, 6020, Innsbruck, Austria.

出版信息

Sci Rep. 2023 Feb 3;13(1):1995. doi: 10.1038/s41598-023-29019-8.

Abstract

DNA metabarcoding is increasingly important for studying feeding interactions, yet it remains unresolved whether reporting read counts or occurrences is to be preferred. To address this issue for gut content samples, basic experimental data on the relationship between read numbers and initial prey DNA amounts and how both change over digestion time is needed. Using regurgitates of the carabid Pseudoophonus rufipes the digestion of Taraxacum officinale seeds was documented for 128 h post-feeding to determine how the number of (1) seed DNA copies and (2) metabarcoding reads change over digestion time, and (3) how they correlate to each other. Additionally, we tested (4) whether PCR cycle-numbers during library preparation affect this correlation. The number of copies and reads both decreased with digestion time, but variation between samples was high. Read and copy numbers correlated when using a library preparation protocol with 35 cycles (R = 42.0%), yet a reduction to 30 cycles might significantly improve this correlation, as indicated by additional PCR testing. Our findings show that protocol optimization is important to reduce technical distortions of read numbers in metabarcoding analysis. However, high inter-sample variation, likely due to variable digestive efficiency of individual consumers, can blur the relationship between the amount of food consumed and metabarcoding read numbers.

摘要

DNA 代谢组学在研究摄食相互作用方面越来越重要,但报告读数值还是出现次数更可取仍未解决。为了解决肠道内容物样本的这个问题,需要有关读数值与初始猎物 DNA 量之间关系的基本实验数据,以及这两者在消化过程中如何随时间变化。本研究使用多食亚目步甲伪步甲的反刍物,记录蒲公英种子的消化过程 128 小时,以确定(1)种子 DNA 拷贝数和(2)代谢组学读数随消化时间如何变化,以及(3)它们如何相互关联。此外,我们还测试了(4)文库制备过程中的 PCR 循环数是否会影响这种相关性。随着消化时间的增加,拷贝数和读数均减少,但样本之间的差异很大。当使用具有 35 个循环的文库制备方案时,读数和拷贝数相关(R=42.0%),但通过额外的 PCR 测试表明,减少到 30 个循环可能会显著改善这种相关性。我们的研究结果表明,方案优化对于减少代谢组学分析中读数值的技术偏差很重要。然而,由于个体消费者的消化效率不同,样本之间的高度差异可能会模糊消耗的食物量和代谢组学读数值之间的关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/622f/9898267/3b62d17289c5/41598_2023_29019_Fig1_HTML.jpg

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