Abstract

Obtaining high-quality samples from wild animals is a major obstacle for genomic studies of many taxa, particularly at the population level, as collection methods for such samples are typically invasive. DNA from feces is easy to obtain noninvasively, but is dominated by bacterial and other non-host DNA. The high proportion of non-host DNA drastically reduces the efficiency of high-throughput sequencing for host animal genomics. To address this issue, we developed an inexpensive capture method for enriching host DNA from noninvasive fecal samples. Our method exploits natural differences in CpG-methylation density between vertebrate and bacterial genomes to preferentially bind and isolate host DNA from majority-bacterial samples. We demonstrate that the enrichment is robust, efficient, and compatible with downstream library preparation methods useful for population studies (e.g., RADseq). Compared to other enrichment strategies, our method is quick and inexpensive, adding only a negligible cost to sample preparation. In combination with downstream methods such as RADseq, our approach allows for cost-effective and customizable genomic-scale genotyping that was previously feasible in practice only with invasive samples. Because feces are widely available and convenient to collect, our method empowers researchers to explore genomic-scale population-level questions in organisms for which invasive sampling is challenging or undesirable.

Highlights

  • The past decade has witnessed a rapid transformation of biological studies with the continuing development and adoption of massively parallel sequencing technology

  • Our enrichment approach captures eukaryotic DNA using a methylated CpG binding domain protein fused to the Fc fragment of human IgG (MBD2-Fc) to selectively target sequences with high CpG methylation density[22]

  • Quantitative PCR estimates of starting host DNA proportions in fecal DNA extracts ranged widely, but were substantially lower in samples obtained from the wild

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Summary

Introduction

The past decade has witnessed a rapid transformation of biological studies with the continuing development and adoption of massively parallel sequencing technology. This sequencing revolution, has far had a relatively muted impact on studies of wild nonmodel organisms due largely to the difficulty of obtaining high-quality samples. This problem is salient for endangered animals, cryptic animals, or animals for which it is otherwise difficult, undesirable, or unethical to obtain samples invasively. Because of the high representation of exogenous DNA in feces, shotgun sequencing of fecal DNA would yield only a small proportion of reads matching the host genome. Without an effective enrichment procedure, sequencing of fecal DNA would be less efficient than that of invasively obtained “high-quality” DNA by at least one order of magnitude regardless of improvements in sequencing throughput or cost

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