The Overlooked Microbiome—Considering Archaea and Eukaryotes Using Multiplex Nanopore-16S-/18S-rDNA-Sequencing: A Technical Report Focusing on Nasopharyngeal Microbiomes

Abstract

In contrast to bacteria, microbiome analyses often neglect archaea, but also eukaryotes. This is partly because they are difficult to culture due to their demanding growth requirements, or some even have to be classified as uncultured microorganisms. Consequently, little is known about the relevance of archaea in human health and diseases. Contemporary broad availability and spread of next generation sequencing techniques now enable a stronger focus on such microorganisms, whose cultivation is difficult. However, due to the enormous evolutionary distances between bacteria, archaea and eukaryotes, the implementation of sequencing strategies for smaller laboratory scales needs to be refined to achieve as a holistic view on the microbiome as possible. Here, we present a technical approach that enables simultaneous analyses of archaeal, bacterial and eukaryotic microbial communities to study their roles in development and courses of respiratory disorders. We thus applied combinatorial 16S-/18S-rDNA sequencing strategies for sequencing-library preparation. Considering the lower total microbiota density of airway surfaces, when compared with gut microbiota, we optimized the DNA purification workflow from nasopharyngeal swab specimens. As a result, we provide a protocol that allows the efficient combination of bacterial, archaeal, and eukaryotic libraries for nanopore-sequencing using Oxford Nanopore Technologies MinION devices and subsequent phylogenetic analyses. In a pilot study, this workflow allowed the identification of some environmental archaea, which were not correlated with airway microbial communities before. Moreover, we assessed the protocol’s broader applicability using a set of human stool samples. We conclude that the proposed protocol provides a versatile and adaptable tool for combinatorial studies on bacterial, archaeal, and eukaryotic microbiomes on a small laboratory scale.

A full‐length 18S ribosomal DNA metabarcoding approach for determining protist community diversity using Nanopore sequencing

“…Until now, most metabarcoding studies of plankton diversity has been assessed using primer pairs that produce fragments lengths <600 bp. For autotropic protists, the 16S plastidal V4‐V5 region was used (Needham & Fuhrman, 2016 ), while short reads of nuclear DNA were used for bacteria, archaea, protist and metazoans (Baehren et al., 2023 ; Curry et al., 2022 ; Davidov et al., 2020 ; Lentendu et al., 2022 ). A short fragment of the ribulose‐1,5‐bisphosphate carboxylase/oxygenase (rbcl) gene was recommended for freshwater diatom diversity (Pérez‐Burillo et al., 2020 ; Vasselon et al., 2017 ).…”