Evidence map›Paper›PMID 22452899›Full record

ArticleBMC microbiology2012

Control of intestinal bacterial proliferation in regulation of lifespan in Caenorhabditis elegans.

Cynthia Portal-Celhay, Ellen R Bradley, Martin J Blaser

Abstract read
In one paragraph

Article in BMC microbiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 118 papers.

0numbers the graph read from it
0cells of the map it votes in
118citing 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

118 citing papers in PubMed.

  1. Gut microbes · 2026
    Review
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  4. Bacterial-derived cyclic lipopeptides suppress dauer arrest inbioRxiv : the preprint server for biology · 2026
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  5. Review
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  8. Gut commensalMicrobiology spectrum · 2026
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  9. Review
  10. Suppression of the fat storage defect ofmicroPublication biology · 2026
    Article
  11. Article
  12. Form and function of actin impacts actin health and aging.bioRxiv : the preprint server for biology · 2025
    Article
  13. The Effects of FeedingMicroorganisms · 2025
    Article
  14. Article
  15. Article
  16. Pantoea piersonii IIIF1SW-P2Scientific reports · 2025
    Article
  17. Article
  18. Article
  19. Article
  20. Article

58 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

3 authors.

Cynthia Portal-CelhayDepartment of Medicine, New York University School of Medicine, NYU Langone Medical Center, 550 First Avenue, OBV A606, New York, NY 10016, USA. portac01@med.nyu.edu
Ellen R Bradley
Martin J Blaser

Funding

MATHEMATICAL MODELS OF H PYLORI GASTRIC COLONIZATIONR01GM063270 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BLASER, MARTIN J · 2000 to 2013
$3.1M
NIGMS NIH HHS R01 GM63270
6 · The paper itself

Abstract

backgroundA powerful approach to understanding complex processes such as aging is to use model organisms amenable to genetic manipulation, and to seek relevant phenotypes to measure. Caenorhabditis elegans is particularly suited to studies of aging, since numerous single-gene mutations have been identified that affect its lifespan; it possesses an innate immune system employing evolutionarily conserved signaling pathways affecting longevity. As worms age, bacteria accumulate in the intestinal tract. However, quantitative relationships between worm genotype, lifespan, and intestinal lumen bacterial load have not been examined. We hypothesized that gut immunity is less efficient in older animals, leading to enhanced bacterial accumulation, reducing longevity. To address this question, we evaluated the ability of worms to control bacterial accumulation as a functional marker of intestinal immunity.

resultsWe show that as adult worms age, several C. elegans genotypes show diminished capacity to control intestinal bacterial accumulation. We provide evidence that intestinal bacterial load, regulated by gut immunity, is an important causative factor of lifespan determination; the effects are specified by bacterial strain, worm genotype, and biologic age, all acting in concert.

conclusionsIn total, these studies focus attention on the worm intestine as a locus that influences longevity in the presence of an accumulating bacterial population. Further studies defining the interplay between bacterial species and host immunity in C. elegans may provide insights into the general mechanisms of aging and age-related diseases.

Indexed as

Bacterial LoadLongevityAnimalsBacteriaCaenorhabditis elegansCaenorhabditis elegans ProteinsGenotypeIntestinesReceptor, InsulinSignal TransductionCaenorhabditis elegans ProteinsDAF-2 protein, C elegansReceptor, Insulin

Identifiers

PMID22452899
PMCPMC3342110

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.