Evidence map›Paper›PMID 31695033›Full record

ArticleNature communications2019

Evaluation of 16S rRNA gene sequencing for species and strain-level microbiome analysis.

Jethro S Johnson, Daniel J Spakowicz, Bo-Young Hong, Lauren M Petersen, Patrick Demkowicz, Lei Chen, Shana R Leopold, Blake M Hanson, Hanako O Agresta, Mark Gerstein and 2 more

Abstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1,164 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1,164citing papers in PubMed, 8 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1,164 citing papers in PubMed, 8 syntheses or guidelines pooled it.

  1. Pooled it
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  7. Systematic Review: Long-Read Sequencing in Algal Studies.International journal of molecular sciences · 2026
    Pooled it
  8. The mosquito gut microbiome andFrontiers in cellular and infection microbiology · 2026
    Pooled it
  9. Assessing the Impact ofNutrients · 2026
    Trial
  10. Article
  11. Article
  12. Article
  13. Article
  14. Effects ofGut microbes · 2026
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

1,104 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Jethro S JohnsonThe Jackson Laboratory for Genomic Medicine, Farmington, CT, 06032, USA. Jethro.Johnson@jax.org.ORCID http://orcid.org/0000-0001-9155-054X
Daniel J SpakowiczThe Jackson Laboratory for Genomic Medicine, Farmington, CT, 06032, USA.ORCID http://orcid.org/0000-0003-2314-6435
Bo-Young HongThe Jackson Laboratory for Genomic Medicine, Farmington, CT, 06032, USA.
Lauren M PetersenThe Jackson Laboratory for Genomic Medicine, Farmington, CT, 06032, USA.
Patrick DemkowiczThe Jackson Laboratory for Genomic Medicine, Farmington, CT, 06032, USA.ORCID http://orcid.org/0000-0002-9566-1033
Lei ChenThe Jackson Laboratory for Genomic Medicine, Farmington, CT, 06032, USA.
Shana R LeopoldThe Jackson Laboratory for Genomic Medicine, Farmington, CT, 06032, USA.
Blake M HansonThe Jackson Laboratory for Genomic Medicine, Farmington, CT, 06032, USA.
Hanako O AgrestaThe Jackson Laboratory for Genomic Medicine, Farmington, CT, 06032, USA.
Mark GersteinDepartment of Computer Science, Yale University, New Haven, CT, USA.
Erica SodergrenThe Jackson Laboratory for Genomic Medicine, Farmington, CT, 06032, USA.
George M WeinstockThe Jackson Laboratory for Genomic Medicine, Farmington, CT, 06032, USA.

Funding

Intestinal bacterial metagenome in pediatric NAFLDR01DK088831 · NIDDK · MEDICAL COLLEGE OF WISCONSIN · PI SALZMAN, NITA H, WEINSTOCK, GEORGE M · 2012 to 2016
$7.0M
NIDDK NIH HHS R01 DK088831
6 · The paper itself

Abstract

The 16S rRNA gene has been a mainstay of sequence-based bacterial analysis for decades. However, high-throughput sequencing of the full gene has only recently become a realistic prospect. Here, we use in silico and sequence-based experiments to critically re-evaluate the potential of the 16S gene to provide taxonomic resolution at species and strain level. We demonstrate that targeting of 16S variable regions with short-read sequencing platforms cannot achieve the taxonomic resolution afforded by sequencing the entire (~1500 bp) gene. We further demonstrate that full-length sequencing platforms are sufficiently accurate to resolve subtle nucleotide substitutions (but not insertions/deletions) that exist between intragenomic copies of the 16S gene. In consequence, we argue that modern analysis approaches must necessarily account for intragenomic variation between 16S gene copies. In particular, we demonstrate that appropriate treatment of full-length 16S intragenomic copy variants has the potential to provide taxonomic resolution of bacterial communities at species and strain level.

Indexed as

Genetic VariationPhylogenyBacteriaBacteriological TechniquesBase SequenceComputational BiologyComputer SimulationDNA, BacterialFecesGene DosageHigh-Throughput Nucleotide SequencingHumansMicrobiotaPolymorphism, GeneticRNA, Ribosomal, 16SSequence Analysis, DNADNA, BacterialRNA, Ribosomal, 16S

Identifiers

PMID31695033
PMCPMC6834636

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.