Evidence map›Paper›PMID 28698568›Full record

ArticleScientific reports2017

An allelic variant of the PmrB sensor kinase responsible for colistin resistance in an Escherichia coli strain of clinical origin.

Antonio Cannatelli, Tommaso Giani, Noemi Aiezza, Vincenzo Di Pilato, Luigi Principe, Francesco Luzzaro, Cesira L Galeotti, Gian Maria Rossolini

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

28 citing papers in PubMed, 54 citations in OpenAlex.

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  9. Global epidemiology, genetic environment, risk factors and therapeutic prospects ofFrontiers in cellular and infection microbiology · 2022
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  11. A Resistance Mechanism in Non-Microbiology spectrum · 2021
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  13. Risk Factors for and Mechanisms ofOpen forum infectious diseases · 2021
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  15. Acquisition of theInfection and drug resistance · 2021
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  17. Infection and immunity · 2020
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  18. A Novel Deletion Mutation inAntimicrobial agents and chemotherapy · 2020
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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

8 authors at 3 institutions in 1 country.

Antonio CannatelliUniversity of Siena, Department of Medical Biotechnologies, Siena, 53100, Italy.
Tommaso GianiUniversity of Siena, Department of Medical Biotechnologies, Siena, 53100, Italy.
Noemi AiezzaUniversity of Siena, Department of Medical Biotechnologies, Siena, 53100, Italy.
Vincenzo Di PilatoUniversity of Florence, Department of Surgery and Translational Medicine, Florence, 50134, Italy.ORCID 0000-0002-5863-5805
Luigi PrincipeLecco A. Manzoni Hospital, Clinical Microbiology and Virology Unit, Lecco, 23900, Italy.
Francesco LuzzaroLecco A. Manzoni Hospital, Clinical Microbiology and Virology Unit, Lecco, 23900, Italy.ORCID 0000-0002-8275-8389
Cesira L GaleottiUniversity of Florence, Department of Experimental and Clinical Medicine, Florence, 50134, Italy.
Gian Maria RossoliniUniversity of Siena, Department of Medical Biotechnologies, Siena, 53100, Italy. gianmaria.rossolini@unifi.it.
University of Siena · ITAlessandro Manzoni Hospital · ITUniversity of Florence · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We investigated the colistin resistance mechanism in an Escherichia coli strain (LC711/14) isolated in Italy in 2014, from an urinary tract infection, which was previously shown to express a colistin resistance mechanism different from mcr-1. LC711/14 was found to carry a novel mutation in the pmrB gene, resulting in a leucine to proline amino acid substitution at position 10 of the PmrB sensor kinase component of the PmrAB signal transduction system. The role of this substitution in colistin resistance was documented by expression of the wild-type and mutated alleles in a pmrB deletion derivative of the E. coli reference strain MG1655, in which expression of the mutated allele conferred colistin resistance and upregulation of the endogenous pmrHFIJKLM lipid A modification system. Complementation of LC711/14 with the wild-type pmrB allele restored colistin susceptibility and decreased expression of pmrHFIJKLM, confirming the role of this PmrB mutation. Substitution of leucine at position 10 of PmrB with other amino acids (glycine and glutamine) resulted in loss of function, underscoring a key role of this residue which is located in the cytoplasmic secretion domain of the protein. This work demonstrated that mutation in this domain of the PmrB sensor kinase can be responsible for acquired colistin resistance in E. coli strains of clinical origin.

Indexed as

AllelesDrug Resistance, BacterialAmino Acid SequenceAmino Acid SubstitutionBacterial ProteinsColistinEscherichia coliHumansMicrobial Sensitivity TestsMutationProtein Structure, SecondaryTranscription FactorsBacterial ProteinsColistinPmrB protein, bacteriaTranscription Factors

Identifiers

PMID28698568
PMCPMC5506025
OpenAlexW2727455448

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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.