High molecular weight DNA extraction strategies for long-read sequencing of complex metagenomes

被引:33
作者
Trigodet, Florian [1 ]
Lolans, Karen [1 ]
Fogarty, Emily [2 ]
Shaiber, Alon [3 ]
Morrison, Hilary G. [4 ]
Barreiro, Luis [1 ]
Jabri, Bana [1 ]
Eren, A. Murat [1 ,2 ,3 ,4 ]
机构
[1] Univ Chicago, Dept Med, Chicago, IL 60637 USA
[2] Univ Chicago, Comm Microbiol, Chicago, IL 60637 USA
[3] Univ Chicago, BioPhys Sci Program, Chicago, IL 60637 USA
[4] Marine Biol Lab, Josephine Bay Paul Ctr Comparat Mol Biol & Evolut, Woods Hole, MA USA
关键词
high-molecular-weight DNA; long-read sequencing; metagenomics; nanopore; ORAL MICROBIOME; NOVO; ALIGNMENT; ARCHAEA;
D O I
10.1111/1755-0998.13588
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
By offering extremely long contiguous characterization of individual DNA molecules, rapidly emerging long-read sequencing strategies offer comprehensive insights into the organization of genetic information in genomes and metagenomes. However, successful long-read sequencing experiments demand high concentrations of highly purified DNA of high molecular weight (HMW), which limits the utility of established DNA extraction kits designed for short-read sequencing. The challenges associated with input DNA quality intensify further when working with complex environmental samples of low microbial biomass, which requires new protocols that are tailored to study metagenomes with long-read sequencing. Here, we use human tongue scrapings to benchmark six HMW DNA extraction strategies that are based on commercially available kits, phenol-chloroform (PC) extraction and agarose encasement followed by agarase digestion. A typical end goal of HMW DNA extractions is to obtain the longest possible reads during sequencing, which is often achieved by PC extractions, as demonstrated in sequencing of cultured cells. Yet our analyses that consider overall read-size distribution, assembly performance and the number of circularized elements found in sequencing results suggest that column-based kits with enzyme supplementation, rather than PC methods, may be more appropriate for long-read sequencing of metagenomes.
引用
收藏
页码:1786 / 1802
页数:17
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