Evidence map›Paper›PMID 23006750›Full record

ArticleAntimicrobial agents and chemotherapy2012

Effect of transcriptional activators SoxS, RobA, and RamA on expression of multidrug efflux pump AcrAB-TolC in Enterobacter cloacae.

Astrid Pérez, Margarita Poza, Jesús Aranda, Cristina Latasa, Francisco Javier Medrano, María Tomás, Antonio Romero, Iñigo Lasa, Germán Bou

Open access · bronzeAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

52 citing papers in PubMed, 85 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Effect of sub-inhibitory tigecycline (½-MIC) on AcrAB-TolC andFrontiers in cellular and infection microbiology · 2026
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. A novel mutation ofMicrobiology spectrum · 2025
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  10. Emergence of concurrently transmissibleMicrobiology spectrum · 2025
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  11. Dual role ofiMetaOmics · 2024
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. A Genetic Locus inAntibiotics (Basel, Switzerland) · 2024
    Article
  17. Article
  18. Review
  19. Efflux Pumps and Different Genetic Contexts ofInternational journal of molecular sciences · 2023
    Article
  20. Characterization of a Tigecycline-Resistant andApplied and environmental microbiology · 2023
    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

9 authors at 4 institutions in 1 country.

Astrid PérezServicio de Microbiología-Instituto de Investigación Biomédica, Complexo Hospitalario Universitario A Coruña, A Coruña, Spain.
Margarita Poza
Jesús Aranda
Cristina Latasa
Francisco Javier Medrano
María Tomás
Antonio Romero
Iñigo Lasa
Germán Bou
Instituto de Investigación Biomédica de A Coruña · ESAgrobiotechnology Institute · ESCentro de Investigaciones Biológicas Margarita Salas · ESComplexo Hospitalario Universitario A Coruña · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Control of membrane permeability is a key step in regulating the intracellular concentration of antibiotics. Efflux pumps confer innate resistance to a wide range of toxic compounds such as antibiotics, dyes, detergents, and disinfectants in members of the Enterobacteriaceae. The AcrAB-TolC efflux pump is involved in multidrug resistance in Enterobacter cloacae. However, the underlying mechanism that regulates the system in this microorganism remains unknown. In Escherichia coli, the transcription of acrAB is upregulated under global stress conditions by proteins such as MarA, SoxS, and Rob. In the present study, two clinical isolates of E. cloacae, EcDC64 (a multidrug-resistant strain overexpressing the AcrAB-TolC efflux pump) and Jc194 (a strain with a basal AcrAB-TolC expression level), were used to determine whether similar global stress responses operate in E. cloacae and also to establish the molecular mechanisms underlying this response. A decrease in susceptibility to erythromycin, tetracycline, telithromycin, ciprofloxacin, and chloramphenicol was observed in clinical isolate Jc194 and, to a lesser extent in EcDC64, in the presence of salicylate, decanoate, tetracycline, and paraquat. Increased expression of the acrAB promoter in the presence of the above-described conditions was observed by flow cytometry and reverse transcription-PCR, by using a reporter fusion protein (green fluorescent protein). The expression level of the AcrAB promoter decreased in E. cloacae EcDC64 derivates deficient in SoxS, RobA, and RamA. Accordingly, the expression level of the AcrAB promoter was higher in E. cloacae Jc194 strains overproducing SoxS, RobA, and RamA. Overall, the data showed that SoxS, RobA, and RamA regulators were associated with the upregulation of acrAB, thus conferring antimicrobial resistance as well as a stress response in E. cloacae. In summary, the regulatory proteins SoxS, RobA, and RamA were cloned and sequenced for the first time in this species. The involvement of these proteins in conferring antimicrobial resistance through upregulation of acrAB was demonstrated in E. cloacae.

Indexed as

Anti-Bacterial AgentsBacterial ProteinsCarrier ProteinsCloning, MolecularCulture MediaDNA, BacterialDrug Resistance, MicrobialElectrophoretic Mobility Shift AssayEnterobacter cloacaeFlow CytometryGenes, ReporterGenetic Complementation TestMicrobial Sensitivity TestsMolecular Sequence DataPlasmidsPolymerase Chain ReactionAcrAB-TolC protein, Enterobacter cloacaeAnti-Bacterial AgentsBacterial ProteinsCarrier ProteinsCulture MediaDNA, BacterialTrans-Activators

Identifiers

PMID23006750
PMCPMC3497196
OpenAlexW2167365239

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.