4.6 Article

Improved Microbial Community Characterization of 16S rRNA via Metagenome Hybridization Capture Enrichment

期刊

FRONTIERS IN MICROBIOLOGY
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fmicb.2021.644662

关键词

amplicon; microbial diversity; microbiome; mock communities; next generation sequencing; shotgun libraries; target enrichment

资金

  1. Center for Disease Control [200-2018-02889 (75D30118C02889)]
  2. US Department of Energy [DE-FC09-07SR22506]
  3. National Institute of Health [R01ES024950, P30ES010126, P42ES031007]
  4. United States Agency for International Development via Peanut and Mycotoxin Innovation Laboratory [ECG-A00-13-00001-00]

向作者/读者索取更多资源

Environmental microbial diversity is commonly studied using methods such as 16S rRNA gene amplicons and shotgun metagenomics. New 16S rRNA sequence capture baits have been developed to combine the advantages of both methods, providing faster and more cost-effective results for investigating microbial communities. These baits have been shown to increase the proportion of 16S rRNA sequences and reduce analysis time, offering an efficient method for assessing bacterial community composition.
Environmental microbial diversity is often investigated from a molecular perspective using 16S ribosomal RNA (rRNA) gene amplicons and shotgun metagenomics. While amplicon methods are fast, low-cost, and have curated reference databases, they can suffer from amplification bias and are limited in genomic scope. In contrast, shotgun metagenomic methods sample more genomic regions with fewer sequence acquisition biases, but are much more expensive (even with moderate sequencing depth) and computationally challenging. Here, we develop a set of 16S rRNA sequence capture baits that offer a potential middle ground with the advantages from both approaches for investigating microbial communities. These baits cover the diversity of all 16S rRNA sequences available in the Greengenes (v. 13.5) database, with no sequence having <78% sequence identity to at least one bait for all segments of 16S. The use of our baits provide comparable results to 16S amplicon libraries and shotgun metagenomic libraries when assigning taxonomic units from 16S sequences within the metagenomic reads. We demonstrate that 16S rRNA capture baits can be used on a range of microbial samples (i.e., mock communities and rodent fecal samples) to increase the proportion of 16S rRNA sequences (average > 400-fold) and decrease analysis time to obtain consistent community assessments. Furthermore, our study reveals that bioinformatic methods used to analyze sequencing data may have a greater influence on estimates of community composition than library preparation method used, likely due in part to the extent and curation of the reference databases considered. Thus, enriching existing aliquots of shotgun metagenomic libraries and obtaining modest numbers of reads from them offers an efficient orthogonal method for assessment of bacterial community composition.

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