Comparative analysis of full-length 16s ribosomal RNA genome sequencing in human fecal samples using primer sets with different degrees of degeneracy
Next-generation sequencing has revolutionized the field of microbiology research and greatly expanded our knowledge of complex bacterial communities. Nanopore sequencing provides distinct advantages, combining costeffectiveness, ease of use, high throughput, and high taxonomic resolution through...
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Main Authors: | , , , , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Philipps-Universität Marburg
2023
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Subjects: | |
Online Access: | PDF Full Text |
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Summary: | Next-generation sequencing has revolutionized the field of microbiology research
and greatly expanded our knowledge of complex bacterial communities.
Nanopore sequencing provides distinct advantages, combining costeffectiveness,
ease of use, high throughput, and high taxonomic resolution
through its ability to process long amplicons, such as the entire 16s rRNA
genome. We examine the performance of the conventional 27F primer (27F-I)
included in the 16S Barcoding Kit distributed by Oxford Nanopore Technologies
(ONT) and that of a more degenerate 27F primer (27F-II) in the context of highly
complex bacterial communities in 73 human fecal samples. The results show
striking differences in both taxonomic diversity and relative abundance of a
substantial number of taxa between the two primer sets. Primer 27F-I reveals a
significantly lower biodiversity and, for example, at the taxonomic level of the
phyla, a dominance of Firmicutes and Proteobacteria as determined by relative
abundances, as well as an unusually high ratio of Firmicutes/Bacteriodetes when
compared to the more degenerate primer set (27F-II). Considering the findings in
the context of the gut microbiomes common in Western industrial societies, as
reported in the American Gut Project, the more degenerate primer set (27F-II)
reflects the composition and diversity of the fecal microbiome significantly better
than the 27F-I primer. This study provides a fundamentally relevant comparative
analysis of the in situ performance of two primer sets designed for sequencing of
the entire 16s rRNA genome and suggests that the more degenerate primer set
(27F-II) should be preferred for nanopore sequencing-based analyses of the
human fecal microbiome. |
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Item Description: | Gefördert durch den Open-Access-Publikationsfonds der UB Marburg. |
DOI: | 10.3389/fgene.2023.1213829 |