Evaluation of methods for the reduction of contaminating host reads when performing shotgun metagenomic sequencing of the milk microbiome

基因组 微生物群 猎枪 生物 深度测序 计算生物学 DNA测序 霰弹枪测序 寄主(生物学) 基因组 纳米孔测序 康蒂格 全基因组测序 细菌基因组大小 人体微生物群 参考基因组 基因组学 顺序装配 仆从 遗传学 DNA 基因
作者
Min Yap,Conor Feehily,Calum J. Walsh,Mark A. Fenelon,Eileen F. Murphy,Fionnuala M. McAuliffe,Douwe van Sinderen,Paul W. O’Toole,Órla O’Sullivan,Paul D. Cotter
出处
期刊:Scientific Reports [Springer Nature]
卷期号:10 (1) 被引量:32
标识
DOI:10.1038/s41598-020-78773-6
摘要

Abstract Shotgun metagenomic sequencing is a valuable tool for the taxonomic and functional profiling of microbial communities. However, this approach is challenging in samples, such as milk, where a low microbial abundance, combined with high levels of host DNA, result in inefficient and uneconomical sequencing. Here we evaluate approaches to deplete host DNA or enrich microbial DNA prior to sequencing using three commercially available kits. We compared the percentage of microbial reads obtained from each kit after shotgun metagenomic sequencing. Using bovine and human milk samples, we determined that host depletion with the MolYsis complete5 kit significantly improved microbial sequencing depth compared to other approaches tested. Importantly, no biases were introduced. Additionally, the increased microbial sequencing depth allowed for further characterization of the microbiome through the generation of metagenome-assembled genomes (MAGs). Furthermore, with the use of a mock community, we compared three common classifiers and determined that Kraken2 was the optimal classifier for these samples. This evaluation shows that microbiome analysis can be performed on both bovine and human milk samples at a much greater resolution without the need for more expensive deep-sequencing approaches.
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