Evidence map›Paper›PMID 14983040›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2004

The genome sequence of the probiotic intestinal bacterium Lactobacillus johnsonii NCC 533.

R David Pridmore, Bernard Berger, Frank Desiere, David Vilanova, Caroline Barretto, Anne-Cecile Pittet, Marie-Camille Zwahlen, Martine Rouvet, Eric Altermann, Rodolphe Barrangou and 5 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 191 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
191citing papers in PubMed, 1 pooled it
64.6field-weighted citation impact, top 1% of its field
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

191 citing papers in PubMed, 1 synthesis or guideline pooled it, 479 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Strain-resolved biology ofFrontiers in veterinary science · 2026
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  5. Multifunctional antimicrobial effects ofFrontiers in immunology · 2026
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  12. Review
  13. Sensoproteomic Characterization ofJournal of agricultural and food chemistry · 2024
    Article
  14. Article
  15. Prebiotic effect of galacto-Applied and environmental microbiology · 2024
    Article
  16. Skin Deep: The Potential of Microbiome Cosmetics.Journal of microbiology (Seoul, Korea) · 2024
    Review
  17. Article
  18. Article
  19. Article
  20. Review

131 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

15 authors at 3 institutions in 3 countries.

R David PridmoreDepartment of Nutrition and Health, Nestlé Research Center, PO Box 44, Vers-chez-les-Blanc, 1000 Lausanne 26, Switzerland. raymond-david.pridmore@rdls.nestle.com
Bernard Berger
Frank Desiere
David Vilanova
Caroline Barretto
Anne-Cecile Pittet
Marie-Camille Zwahlen
Martine Rouvet
Eric Altermann
Rodolphe Barrangou
Beat Mollet
Annick Mercenier
Todd Klaenhammer
Fabrizio Arigoni
Mark A Schell
North Carolina State University · USUniversity of Georgia · USNestlé (Switzerland) · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lactobacillus johnsonii NCC 533 is a member of the acidophilus group of intestinal lactobacilli that has been extensively studied for their "probiotic" activities that include, pathogen inhibition, epithelial cell attachment, and immunomodulation. To gain insight into its physiology and identify genes potentially involved in interactions with the host, we sequenced and analyzed the 1.99-Mb genome of L. johnsonii NCC 533. Strikingly, the organism completely lacked genes encoding biosynthetic pathways for amino acids, purine nucleotides, and most cofactors. In apparent compensation, a remarkable number of uncommon and often duplicated amino acid permeases, peptidases, and phosphotransferase-type transporters were discovered, suggesting a strong dependency of NCC 533 on the host or other intestinal microbes to provide simple monomeric nutrients. Genome analysis also predicted an abundance (>12) of large and unusual cell-surface proteins, including fimbrial subunits, which may be involved in adhesion to glycoproteins or other components of mucin, a characteristic expected to affect persistence in the gastrointestinal tract (GIT). Three bile salt hydrolases and two bile acid transporters, proteins apparently critical for GIT survival, were also detected. In silico genome comparisons with the >95% complete genome sequence of the closely related Lactobacillus gasseri revealed extensive synteny punctuated by clear-cut insertions or deletions of single genes or operons. Many of these regions of difference appear to encode metabolic or structural components that could affect the organisms competitiveness or interactions with the GIT ecosystem.

Indexed as

Genome, BacterialBiological TransportCell AdhesionEnergy MetabolismFimbriae, BacterialGenes, BacterialHumansIntestinal MucosaLactobacillusMolecular Sequence DataOperon

Identifiers

PMID14983040
PMCPMC356981
OpenAlexW1997370001

What OpenQuestion holds

Textmetadata
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.