Abstract

The human intestinal microbiota is abundant in viruses, comprising mainly bacteriophages, occasionally outnumbering bacteria 10:1 and is termed the virome. Due to their high genetic diversity and the lack of suitable tools and reference databases, the virome remains poorly characterised and is often referred to as “viral dark matter”. However, the choice of sequencing platforms, read lengths and library preparation make study design challenging with respect to the virome. Here we have compared the use of PCR and PCR-free methods for sequence-library construction on the Illumina sequencing platform for characterising the human faecal virome. Viral DNA was extracted from faecal samples of three healthy donors and sequenced. Our analysis shows that most variation was reflecting the individually specific faecal virome. However, we observed differences between PCR and PCR-free library preparation that affected the recovery of low-abundance viral genomes. Using three faecal samples in this study, the PCR library preparation samples led to a loss of lower-abundance vOTUs evident in their PCR-free pairs (vOTUs 128, 6202 and 8364) and decreased the alpha-diversity indices (Chao1 p-value = 0.045 and Simpson p-value = 0.044). Thus, differences between PCR and PCR-free methods are important to consider when investigating “rare” members of the gut virome, with these biases likely negligible when investigating moderately and highly abundant viruses.

Highlights

  • The human intestinal microbiota is increasingly recognised as playing an essential role in health, contributing to digestion and the provision of essential micronutrients, and maintaining immune homeostasis and resisting infection [1,2]

  • This study was approved by the University of East Anglia (UEA) Faculty of Medicine and Health Sciences (FMH) Research Ethics Committee (FMH20142015-28), Norwich in 2014, and by the Health Research Authority (HRA) NRES Committee (17/LO/1102; IRAS: 218545) in 2017

  • To assess the efficiency of viruslike particles (VLPs) recovery, samples were spiked with the reference phage ΦB124-14 to quantify phage recovery by plaque assays and epifluorescence microscopy (EFM; see Method S1 in Supplementary Materials)

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Summary

Introduction

The human intestinal microbiota is increasingly recognised as playing an essential role in health, contributing to digestion and the provision of essential micronutrients, and maintaining immune homeostasis and resisting infection [1,2]. It consists of complex dynamic communities of bacteria, viruses, fungi, archaea and protozoa among which viruses (the virome) dominate numerically [3,4,5,6]. Phages (the phageome) make up more than 90% of the virome [3,5] with their ability to kill or alter the phenotype and function of their host cells enabling them to contribute to maintaining or disrupting intestinal homeostasis. Metagenomics—a powerful sequence-based means of analysing the composition of the collective microbial genomes within an environmental sample—is currently the most reliable to survey the human virome

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