Evidence map›Paper›PMID 25059827›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2014

Enteric dysbiosis promotes antibiotic-resistant bacterial infection: systemic dissemination of resistant and commensal bacteria through epithelial transcytosis.

Linda Chia-Hui Yu, Yi-An Shih, Li-Ling Wu, Yang-Ding Lin, Wei-Ting Kuo, Wei-Hao Peng, Kuo-Shyan Lu, Shu-Chen Wei, Jerrold R Turner, Yen-Hsuan Ni

Abstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

56 citing papers in PubMed, 80 citations in OpenAlex.

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  9. Evaluation of extended-spectrumFrontiers in microbiology · 2025
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  10. Fecal Carriage of Multidrug-ResistantBioMed research international · 2025
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  11. Molecular medicine reports · 2024
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  16. The implication of gut microbiota in recovery from gastrointestinal surgery.Frontiers in cellular and infection microbiology · 2023
    Review
  17. Review
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  19. Prevalence and Implications of Shiga Toxin-ProducingPathogens (Basel, Switzerland) · 2022
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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

10 authors at 3 institutions in 2 countries.

Linda Chia-Hui YuGraduate Institute of Physiology, National Taiwan University College of Medicine and Hospital, Taipei, Taiwan;
Yi-An ShihGraduate Institute of Physiology, National Taiwan University College of Medicine and Hospital, Taipei, Taiwan;
Li-Ling WuGraduate Institute of Physiology, National Taiwan University College of Medicine and Hospital, Taipei, Taiwan;
Yang-Ding LinDepartment of Pediatrics, National Taiwan University College of Medicine, Taipei, Taiwan;
Wei-Ting KuoGraduate Institute of Physiology, National Taiwan University College of Medicine and Hospital, Taipei, Taiwan;
Wei-Hao PengGraduate Institute of Anatomy and Cell Biology, National Taiwan University College of Medicine, Taipei, Taiwan;
Kuo-Shyan LuGraduate Institute of Anatomy and Cell Biology, National Taiwan University College of Medicine, Taipei, Taiwan;
Shu-Chen WeiDepartment of Internal Medicine, National Taiwan University College of Medicine and Hospital, Taipei, Taiwan; and.
Jerrold R TurnerDepartment of Pathology, University of Chicago, Chicago, Illinois.
Yen-Hsuan NiDepartment of Pediatrics, National Taiwan University College of Medicine, Taipei, Taiwan; yhni@ntu.edu.tw.
National Taiwan University Hospital · TWNational Taiwan University · TWUniversity of Chicago · US

Funding

ZO-1-MEDIATED PROTEIN INTERACTIONS: REGULATORS AND INTEGRATORS OF DIVERSE EPITHELIAL FUNCTIONS IN HEALTH AND DISEASER01DK061931 · NIDDK · UNIVERSITY OF CHICAGO · PI JERROLD R. TURNER · 2001 to 2026
$15.0M
Therapeutic targeting of protein interactions to reverse MLCK1-mediated intestinal barrier loss and ameliorate disease.R01DK068271 · NIDDK · UNIVERSITY OF CHICAGO · PI JERROLD R. TURNER · 2005 to 2026
$11.3M
NIDDK NIH HHS R01 DK068271
6 · The paper itself

Abstract

Antibiotic usage promotes intestinal colonization of antibiotic-resistant bacteria. However, whether resistant bacteria gain dominance in enteric microflora or disseminate to extraintestinal viscera remains unclear. Our aim was to investigate temporal diversity changes in microbiota and transepithelial routes of bacterial translocation after antibiotic-resistant enterobacterial colonization. Mice drinking water with or without antibiotics were intragastrically gavaged with ampicillin-resistant (Amp-r) nonpathogenic Escherichia coli (E. coli) and given normal water afterward. The composition and spatial distribution of intestinal bacteria were evaluated using 16S rDNA sequencing and fluorescence in situ hybridization. Bacterial endocytosis in epithelial cells was examined using gentamicin resistance assay and transmission electromicroscopy. Paracellular permeability was assessed by tight junctional immunostaining and measured by tissue conductance and luminal-to-serosal dextran fluxes. Our results showed that antibiotic treatment enabled intestinal colonization and transient dominance of orally acquired Amp-r E. coli in mice. The colonized Amp-r E. coli peaked on day 3 postinoculation and was competed out after 1 wk, as evidenced by the recovery of commensals, such as Escherichia, Bacteroides, Lachnospiraceae, Clostridium, and Lactobacillus. Mucosal penetration and extraintestinal dissemination of exogenous and endogenous enterobacteria were correlated with abnormal epithelial transcytosis but uncoupled with paracellular tight junctional damage. In conclusion, antibiotic-induced enteric dysbiosis predisposes to exogenous infection and causes systemic dissemination of both antibiotic-resistant and commensal enterobacteria through transcytotic routes across epithelial layers. These results may help explain the susceptibility to sepsis in antibiotic-resistant enteric bacterial infection.

Indexed as

Drug Resistance, MicrobialMicrobiotaSymbiosisTranscytosisAmpicillinAnimalsAnti-Bacterial AgentsDysbiosisEnterobacteriaceae InfectionsEscherichia coliIntestinal MucosaMiceMice, Inbred BALB CMice, Inbred C57BLAmpicillinAnti-Bacterial Agentsbacterial endocytosisepithelial barriergut-derived sepsisintestinal microbiotasuperbug

Identifiers

PMID25059827
PMCPMC4214854
OpenAlexW2314306274

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.