Evidence map›Paper›PMID 24558463›Full record

ArticlePloS one2014

Lactobacillus zeae protects Caenorhabditis elegans from enterotoxigenic Escherichia coli-caused death by inhibiting enterotoxin gene expression of the pathogen.

Mengzhou Zhou, Hai Yu, Xianhua Yin, Parviz M Sabour, Wei Chen, Joshua Gong

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.5field-weighted citation impact, top 22% 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

32 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Article
  3. Functional evaluation of synbiotic combination ofCurrent research in food science · 2025
    Article
  4. Review
  5. Functional evaluation ofTranslational animal science · 2024
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Marine drugs · 2021
    Article
  12. Frontiers in immunology · 2021
    Article
  13. Frontiers in cellular and infection microbiology · 2021
    Article
  14. Article
  15. Article
  16. Caenorhabditis elegans: a model to understand host-microbe interactions.Cellular and molecular life sciences : CMLS · 2020
    Review
  17. Article
  18. Article
  19. Frontiers in nutrition · 2020
    Review
  20. BioMed research international · 2020
    Article
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

6 authors at 2 institutions in 2 countries.

Mengzhou ZhouState Key Laboratory of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu, China ; Guelph Food Research Centre, Agriculture and Agri-Food Canada, Guelph, Ontario, Canada.
Hai YuGuelph Food Research Centre, Agriculture and Agri-Food Canada, Guelph, Ontario, Canada.
Xianhua YinGuelph Food Research Centre, Agriculture and Agri-Food Canada, Guelph, Ontario, Canada.
Parviz M SabourGuelph Food Research Centre, Agriculture and Agri-Food Canada, Guelph, Ontario, Canada.
Wei ChenState Key Laboratory of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu, China.
Joshua GongGuelph Food Research Centre, Agriculture and Agri-Food Canada, Guelph, Ontario, Canada.
Agriculture and Agri-Food Canada · CAState Key Laboratory of Food Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe nematode Caenorhabditis elegans has become increasingly used for screening antimicrobials and probiotics for pathogen control. It also provides a useful tool for studying microbe-host interactions. This study has established a C. elegans life-span assay to preselect probiotic bacteria for controlling K88(+) enterotoxigenic Escherichia coli (ETEC), a pathogen causing pig diarrhea, and has determined a potential mechanism underlying the protection provided by Lactobacillus. METHODOLOGY/PRINCIPAL

findingsLife-span of C. elegans was used to measure the response of worms to ETEC infection and protection provided by lactic acid-producing bacteria (LAB). Among 13 LAB isolates that varied in their ability to protect C. elegans from death induced by ETEC strain JG280, Lactobacillus zeae LB1 offered the highest level of protection (86%). The treatment with Lactobacillus did not reduce ETEC JG280 colonization in the nematode intestine. Feeding E. coli strain JFF4 (K88(+) but lacking enterotoxin genes of estA, estB, and elt) did not cause death of worms. There was a significant increase in gene expression of estA, estB, and elt during ETEC JG280 infection, which was remarkably inhibited by isolate LB1. The clone with either estA or estB expressed in E. coli DH5α was as effective as ETEC JG280 in killing the nematode. However, the elt clone killed only approximately 40% of worms. The killing by the clones could also be prevented by isolate LB1. The same isolate only partially inhibited the gene expression of enterotoxins in both ETEC JG280 and E. coli DH5α in-vitro. CONCLUSIONS/SIGNIFICANCE: The established life-span assay can be used for studies of probiotics to control ETEC (for effective selection and mechanistic studies). Heat-stable enterotoxins appeared to be the main factors responsible for the death of C. elegans. Inhibition of ETEC enterotoxin production, rather than interference of its intestinal colonization, appears to be the mechanism of protection offered by Lactobacillus.

Indexed as

Analysis of VarianceAnimalsCaenorhabditis elegansCloning, MolecularEnterotoxigenic Escherichia coliEnterotoxinsGene Expression Regulation, BacterialIntestinesLactobacillusMicroscopy, Electron, TransmissionProbioticsReal-Time Polymerase Chain ReactionReverse Transcriptase Polymerase Chain ReactionSpecies SpecificitySurvival AnalysisEnterotoxins

Identifiers

PMID24558463
PMCPMC3928337
OpenAlexW1990898134

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.