Abstract

In studies of the human microbiome, faecal samples are frequently used as a non-invasive proxy for the study of the intestinal microbiota. To obtain reliable insights, the need for bacterial DNA of high quality and integrity following appropriate faecal sample collection and preservation steps is paramount. In a study of dietary mineral balance in the context of type 2 diabetes (T2D), faecal samples were collected from healthy and T2D individuals throughout a 13-day residential trial. These samples were freeze-dried, then stored mostly at -20°C from the trial date in 2000/2001 until the current research in 2014. Given the relative antiquity of these samples (~14 years), we sought to evaluate DNA quality and comparability to freshly collected human faecal samples. Following the extraction of bacterial DNA, gel electrophoresis indicated that our DNA extracts were more sheared than extracts made from freshly collected faecal samples, but still of sufficiently high molecular weight to support amplicon-based studies. Likewise, spectrophotometric assessment of extracts revealed that they were of high quality and quantity. A subset of bacterial 16S rRNA gene amplicons were sequenced using Illumina MiSeq and compared against publicly available sequence data representing a similar cohort analysed by the American Gut Project (AGP). Notably, our bacterial community profiles were highly consistent with those from the AGP data. Our results suggest that when faecal specimens are stored appropriately, the microbial profiles are preserved and robust to extended storage periods.

Highlights

  • Our understanding of the gut microbiota and its role in human health has benefitted immensely from recent technological advances

  • In the absence of an appropriate microbiota data set for New Zealand individuals, we compared our sequence data with those obtained from faecal samples analysed by the American Gut Project (AGP)

  • In addition to the extensive metadata collected by the AGP which allowed us to stratify our cohort as rigidly as possible, the post-storage processing of faecal samples from the AGP is similar to the approach used in our study, i.e. the same DNA extraction kit and Illumina sequencing technologies were employed

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Summary

Introduction

Our understanding of the gut microbiota and its role in human health has benefitted immensely from recent technological advances. Comparison of 16S rRNA gene sequences with data obtained from a similar cohort We selected 13 of the freeze-dried faecal samples derived from the cohort of healthy individuals of Cooper et al [7] (S1 Table) and sequenced the 16S rRNA genes.

Results
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