Evidence map›Paper›PMID 25807080›Full record

ArticlePloS one2015

Characterization of MATE-type multidrug efflux pumps from Klebsiella pneumoniae MGH78578.

Wakano Ogawa, Yusuke Minato, Hayata Dodan, Motoyasu Onishi, Tomofusa Tsuchiya, Teruo Kuroda

Abstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Antibiotic Resistance inAntibiotics (Basel, Switzerland) · 2026
    Review
  2. Article
  3. Review
  4. Review
  5. Pangenomic analysis ofFrontiers in microbiology · 2022
    Article
  6. Review
  7. A Molecular Perspective on Colistin andDiagnostics (Basel, Switzerland) · 2021
    Review
  8. Article
  9. Review
  10. Correlation between antimicrobial resistance and virulence in Klebsiella pneumoniae.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2016
    Review
  11. 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.

Wakano OgawaDepartment of Microbiology and Biochemistry, Daiichi University of Pharmacy, Fukuoka, Japan; Department of Microbiology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama, Japan.
Yusuke MinatoDepartment of Microbiology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama, Japan.
Hayata DodanDepartment of Microbiology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama, Japan.
Motoyasu OnishiDepartment of Microbiology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama, Japan.
Tomofusa TsuchiyaDepartment of Microbiology, College of Pharmaceutical Sciences, Ritsumeikan University, Shiga, Japan.
Teruo KurodaDepartment of Microbiology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We previously described the cloning of genes related to drug resistance from Klebsiella pneumoniae MGH78578. Of these, we identified a putative gene encoding a MATE-type multidrug efflux pump, and named it ketM. Escherichia coli KAM32 possessing ketM on a plasmid showed increased minimum inhibitory concentrations for norfloxacin, ciprofloxacin, cefotaxime, acriflavine, Hoechst 33342, and 4',6-diamidino-2-phenyl indole (DAPI). The active efflux of DAPI was observed in E. coli KAM32 possessing ketM on a plasmid. The expression of mRNA for ketM was observed in K. pneumoniae cells, and we subsequently disrupted ketM in K. pneumoniae ATCC10031. However, no significant changes were observed in drug resistance levels between the parental strain ATCC10031 and ketM disruptant, SKYM. Therefore, we concluded that KetM was a multidrug efflux pump, that did not significantly contribute to intrinsic resistance to antimicrobial chemicals in K. pneumoniae. MATE-type transporters are considered to be secondary transporters; therefore, we investigated the coupling cations of KetM. DAPI efflux by KetM was observed when lactate was added to produce a proton motive force, indicating that KetM effluxed substrates using a proton motive force. However, the weak efflux of DAPI by KetM was also noted when NaCl was added to the assay mixture without lactate. This result suggests that KetM may utilize proton and sodium motive forces.

Indexed as

Amino Acid SequenceAnti-Bacterial AgentsBacterial ProteinsCloning, MolecularDrug Resistance, Multiple, BacterialEscherichia coliKlebsiella pneumoniaeMembrane Transport ProteinsMicrobial Sensitivity TestsMolecular Sequence DataPlasmidsProton-Motive ForceRNA, MessengerSequence AlignmentAnti-Bacterial AgentsBacterial ProteinsMembrane Transport ProteinsRNA, Messenger

Identifiers

PMID25807080
PMCPMC4373734

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Registered trials

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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.