Heterogeneity spacers in 16S rDNA primers improve analysis of mouse gut microbiomes via greater nucleotide diversity

BioTechniques

William H Broach¹  Edward O List²  Darlene E Berryman²  Erin R Murphy²  Elizabeth A Jensen²  Ronan K Carroll²  Joshua Busken³ 

[1] 10Ohio University Genomics Facility, Ohio University, Athens, OH 45701, USA;1Department of Translational Biomedical Sciences, Graduate College, Ohio University, Athens, OH, USA;3The Diabetes Institute, Konneker Research Center 108, Ohio University, Athens, OH 45701, USA;

关键词: 16S rDNA sequencing;    microbiome;    optimization;    primer design;    V3–V4 region;   

DOI  :  10.2144/btn-2019-0025

来源: DOAJ

【 摘 要 】

Illumina-based amplicon sequencing suffers from the deleterious effects of highly homogenous nucleotide composition, limiting the number of high-quality reads generated per run. We attempted to alleviate this limitation by comparing the results obtained from 16S ribosomal DNA (16S rDNA) sequencing of mouse gut microbiomes using Illumina V3–V4 primers (Run 1) and custom primers that incorporate a heterogeneity spacer (0–7 nucleotides) upstream of the 16S priming region (Run 2). Overall, Run 2 had higher quality sequences, a more diverse microbial profile, and higher precision within, and variation between, experimental groups than Run 1. Our primer design offers a simple way to increase the quality of 16S rDNA sequencing and increases the number of useable reads generated per Illumina run.

【 授权许可】

Unknown