Scinovex
article Open AccessTop 1% cited

Exploring Microbial Diversity and Taxonomy Using SSU rRNA Hypervariable Tag Sequencing

PLoS Genetics · 2008 · Vol. 4(11) · pp. e1000255–e1000255
Susan M. HuseLes DethlefsenJulie A. HuberDavid B. Mark WelchDavid A. RelmanMitchell L. Sogin

Abstract

Massively parallel pyrosequencing of hypervariable regions from small subunit ribosomal RNA (SSU rRNA) genes can sample a microbial community two or three orders of magnitude more deeply per dollar and per hour than capillary sequencing of full-length SSU rRNA. As with full-length rRNA surveys, each sequence read is a tag surrogate for a single microbe. However, rather than assigning taxonomy by creating gene trees de novo that include all experimental sequences and certain reference taxa, we compare the hypervariable region tags to an extensive database of rRNA sequences and assign taxonomy based on the best match in a Global Alignment for Sequence Taxonomy (GAST) process. The resulting taxonomic census provides information on both composition and diversity of the microbial community. To determine the effectiveness of using only hypervariable region tags for assessing microbial community membership, we compared the taxonomy assigned to the V3 and V6 hypervariable regions with the taxonomy assigned to full-length SSU rRNA sequences isolated from both the human gut and a deep-sea hydrothermal vent. The hypervariable region tags and full-length rRNA sequences provided equivalent taxonomy and measures of relative abundance of microbial communities, even for tags up to 15% divergent from their nearest reference match. The greater sampling depth per dollar afforded by massively parallel pyrosequencing reveals many more members of the "rare biosphere" than does capillary sequencing of the full-length gene. In addition, tag sequencing eliminates cloning bias and the sequences are short enough to be completely sequenced in a single read, maximizing the number of organisms sampled in a run while minimizing chimera formation. This technique allows the cost-effective exploration of changes in microbial community structure, including the rare biosphere, over space and time and can be applied immediately to initiatives, such as the Human Microbiome Project.

Microbial Community Ecology and PhysiologyGenomics and Phylogenetic StudiesMethane Hydrates and Related PhenomenaBiologyHypervariable regionPyrosequencingRibosomal RNAEvolutionary biologyMassive parallel sequencingGeneticsTaxonomy (biology)Computational biologyDNA sequencing

MeSH terms

BacteriaClassificationHumansRNA, RibosomalSequence Tagged SitesSequence Analysis, DNABiodiversityMetagenome

Funding

  • National Science Foundation
  • National Institutes of Health
  • National Institute of Environmental Health Sciences
Citations
1,009
FWCI
54.73
field-weighted impact
References
43
Percentile
100%
vs. same field & year
Citations per year
References
Greengenes, a Chimera-Checked 16S rRNA Gene Database and Workbench Compatible with ARB
Applied and Environmental Microbiology · 2006 · 11,173 citations
EMBOSS: The European Molecular Biology Open Software Suite
Trends in Genetics · 2000 · 9,735 citations
Pyrosequencing enumerates and contrasts soil microbial diversity
The ISME Journal · 2007 · 1,852 citations
Basic local alignment search tool
Journal of Molecular Biology · 1990 · 93,570 citations
Bacteria of Dental Caries in Primary and Permanent Teeth in Children and Young Adults
Journal of Clinical Microbiology · 2008 · 951 citations
Prokaryotes: The unseen majority
Proceedings of the National Academy of Sciences · 1998 · 4,788 citations
Related articles
Accuracy and quality of massively parallel DNA pyrosequencing
Genome biology · 2007 · 1,295 citations
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.