Evidence map›Paper›PMID 25788514›Full record

ReviewClinical microbiology reviews2015

The challenge of efflux-mediated antibiotic resistance in Gram-negative bacteria.

Xian-Zhi Li, Patrick Plésiat, Hiroshi Nikaido

Abstract readReview
In one paragraph

Review in Clinical microbiology reviews, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 807 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
807citing papers in PubMed, 1 pooled it
–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

807 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. High resolution cryo-EM structure of theJournal of structural biology: X · 2026
    Article
  4. Article
  5. Review
  6. Review
  7. New microbes and new infections · 2026
    Review
  8. Heterogeneity of azithromycin resistance markers inNew microbes and new infections · 2026
    Review
  9. Global epidemiology of carbapenem-resistantJAC-antimicrobial resistance · 2026
    Review
  10. Article
  11. Article
  12. Article
  13. Adaptive Response ofAntibiotics (Basel, Switzerland) · 2026
    Article
  14. Callus Induction inPlants (Basel, Switzerland) · 2026
    Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. Detection of an ExPEC-likeBiotech (Basel (Switzerland)) · 2026
    Article

747 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.

Xian-Zhi LiHuman Safety Division, Veterinary Drugs Directorate, Health Products and Food Branch, Health Canada, Ottawa, Ontario, Canada.ORCID http://orcid.org/0000-0003-1722-3254
Patrick PlésiatLaboratoire de Bactériologie, Faculté de Médecine-Pharmacie, Centre Hospitalier Régional Universitaire, Université de Franche-Comté, Besançon, France.
Hiroshi NikaidoDepartment of Molecular and Cell Biology, University of California, Berkeley, California, USA nhiroshi@berkeley.edu.

Funding

BIOCHEMISTRY OF BACTERIAL CELL MEMBRANESR01AI009644 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI NIKAIDO, HIROSHI · 1985 to 2015
$9.7M
BIOCHEMISTRY OF BACTERIAL CELL MEMBRANESR37AI009644 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI NIKAIDO, HIROSHI · 1991 to 2000
$467k
NIAID NIH HHS AI-09644NIAID NIH HHS R01 AI009644NIAID NIH HHS R37 AI009644
6 · The paper itself

Abstract

The global emergence of multidrug-resistant Gram-negative bacteria is a growing threat to antibiotic therapy. The chromosomally encoded drug efflux mechanisms that are ubiquitous in these bacteria greatly contribute to antibiotic resistance and present a major challenge for antibiotic development. Multidrug pumps, particularly those represented by the clinically relevant AcrAB-TolC and Mex pumps of the resistance-nodulation-division (RND) superfamily, not only mediate intrinsic and acquired multidrug resistance (MDR) but also are involved in other functions, including the bacterial stress response and pathogenicity. Additionally, efflux pumps interact synergistically with other resistance mechanisms (e.g., with the outer membrane permeability barrier) to increase resistance levels. Since the discovery of RND pumps in the early 1990s, remarkable scientific and technological advances have allowed for an in-depth understanding of the structural and biochemical basis, substrate profiles, molecular regulation, and inhibition of MDR pumps. However, the development of clinically useful efflux pump inhibitors and/or new antibiotics that can bypass pump effects continues to be a challenge. Plasmid-borne efflux pump genes (including those for RND pumps) have increasingly been identified. This article highlights the recent progress obtained for organisms of clinical significance, together with methodological considerations for the characterization of MDR pumps.

Indexed as

AnimalsAnti-Bacterial AgentsDrug Resistance, MicrobialGram-Negative BacteriaHumansMembrane Transport ProteinsAnti-Bacterial AgentsMembrane Transport Proteins

Identifiers

PMID25788514
PMCPMC4402952

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.