Evidence map›Paper›PMID 21149389›Full record

ArticleGenome research2011

Analysis of streptococcal CRISPRs from human saliva reveals substantial sequence diversity within and between subjects over time.

David T Pride, Christine L Sun, Julia Salzman, Nitya Rao, Peter Loomer, Gary C Armitage, Jillian F Banfield, David A Relman

Abstract read
In one paragraph

Article in Genome research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed
–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

65 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Correlation between CRISPR Loci Diversity in Three Enterobacterial Taxa.International journal of molecular sciences · 2022
    Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Lysogeny inMicroorganisms · 2020
    Review
  12. Review
  13. Natural diversity of CRISPR spacers of Thermus: evidence of local spacer acquisition and global spacer exchange.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2019
    Article
  14. Diversified local CRISPR-Cas immunity to viruses of Sulfolobus islandicus.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2019
    Article
  15. Article
  16. Article
  17. Review
  18. How adaptive immunity constrains the composition and fate of large bacterial populations.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  19. Article
  20. Article

5 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

8 authors.

David T PrideDepartment of Pathology, University of California, San Diego, La Jolla, California 92093, USA.
Christine L Sun
Julia Salzman
Nitya Rao
Peter Loomer
Gary C Armitage
Jillian F Banfield
David A Relman

Funding

NIH Director's Pioneer AwardDP1OD000964 · OD · STANFORD UNIVERSITY · PI RELMAN, DAVID A. · 2006 to 2010
$3.4M
NIH HHS DP1 OD000964NIH HHS DP1OD000964
6 · The paper itself

Abstract

Viruses may play an important role in the evolution of human microbial communities. Clustered regularly interspaced short palindromic repeats (CRISPRs) provide bacteria and archaea with adaptive immunity to previously encountered viruses. Little is known about CRISPR composition in members of human microbial communities, the relative rate of CRISPR locus change, or how CRISPR loci differ between the microbiota of different individuals. We collected saliva from four periodontally healthy human subjects over an 11- to 17-mo time period and analyzed CRISPR sequences with corresponding streptococcal repeats in order to improve our understanding of the predominant features of oral streptococcal adaptive immune repertoires. We analyzed a total of 6859 CRISPR bearing reads and 427,917 bacterial 16S rRNA gene sequences. We found a core (ranging from 7% to 22%) of shared CRISPR spacers that remained stable over time within each subject, but nearly a third of CRISPR spacers varied between time points. We document high spacer diversity within each subject, suggesting constant addition of new CRISPR spacers. No greater than 2% of CRISPR spacers were shared between subjects, suggesting that each individual was exposed to different virus populations. We detect changes in CRISPR spacer sequence diversity over time that may be attributable to locus diversification or to changes in streptococcal population structure, yet the composition of the populations within subjects remained relatively stable. The individual-specific and traceable character of CRISPR spacer complements could potentially open the way for expansion of the domain of personalized medicine to the oral microbiome, where lineages may be tracked as a function of health and other factors.

Indexed as

Genetic VariationDNA, BacterialDNA, IntergenicEcosystemHumansInverted Repeat SequencesPhylogenyRNA, Ribosomal, 16SSalivaSequence Analysis, DNAStreptococcusDNA, BacterialDNA, IntergenicRNA, Ribosomal, 16S

Identifiers

PMID21149389
PMCPMC3012920

What OpenQuestion holds

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Read underepoch 390

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.