Evidence map›Paper›PMID 27458841›Full record

ReviewCurrent opinion in microbiology2016

Targeting cell membrane adaptation as a novel antimicrobial strategy.

Truc T Tran, William R Miller, Yousif Shamoo, Cesar A Arias

Abstract readReview
In one paragraph

Review in Current opinion in microbiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Review
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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

4 authors.

Truc T TranDivision of Infectious Diseases, Department of Internal Medicine, University of Texas McGovern Medical School, Houston, TX, United States; Center for Antibiotic Resistance and Microbial Genomics, University of Texas McGovern Medical School, Houston, TX, United States.
William R MillerDivision of Infectious Diseases, Department of Internal Medicine, University of Texas McGovern Medical School, Houston, TX, United States; Center for Antibiotic Resistance and Microbial Genomics, University of Texas McGovern Medical School, Houston, TX, United States.
Yousif ShamooDepartment of Biochemistry and Cell Biology, Rice University, Houston, TX, United States.
Cesar A AriasDivision of Infectious Diseases, Department of Internal Medicine, University of Texas McGovern Medical School, Houston, TX, United States; Center for Antibiotic Resistance and Microbial Genomics, University of Texas McGovern Medical School, Houston, TX, United States; Molecular Genetics and Antimicrobial Resistance Unit, Universidad El Bosque, Bogota, Colombia; International Center for Microbial Genomics, Universidad El Bosque, Bogota, Colombia. Electronic address: cesar.arias@uth.tmc.edu.

Funding

Defining Evolutionary Trajectories: Molecular adaptation to antibiotic resistanceR01AI080714 · NIAID · RICE UNIVERSITY · PI SHAMOO, YOUSIF · 2009 to 2023
$4.3M
Molecular Mechanisms Of Daptomycin Resistance In EnterococciR01AI093749 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI ARIAS, CESAR AUGUSTO · 2011 to 2015
$1.9M
POR Program on Genomic Prediction of Antimicrobial Resistance in VREK24AI121296 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI ARIAS, CESAR AUGUSTO · 2016 to 2025
$1.5M
Daptomycin Resistance in Enterococcus faeciumK08AI113317 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI TRAN, TRUC THANH · 2014 to 2018
$792k
Characterization of LiaR from multidrug-resistant E. faeciumR21AI114961 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI ARIAS, CESAR AUGUSTO · 2015 to 2016
$438k
Targeting Cell Membrane Adaptation in Multidrug-Resistant Enterococcus faeciumR21AI121519 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI ARIAS, CESAR AUGUSTO · 2016 to 2017
$226k
NIAID NIH HHS K08 AI113317NIAID NIH HHS K24 AI121296NIAID NIH HHS R01 AI080714NIAID NIH HHS R01 AI093749NIAID NIH HHS R21 AI114961NIAID NIH HHS R21 AI121519
6 · The paper itself

Abstract

Emergence of antibiotic resistance is an example of the incredible plasticity of bacteria to survive in all environments. The search for new antibiotics active against traditional targets is more challenging due not only to the lack of novel natural products to fulfill the current clinical needs against multidrug-resistant (MDR) bacteria, but also for the possible 'collateral' effects on the human microbiota. Thus, non-traditional approaches to combat MDR bacteria have been proposed. Here, we discuss the possibility of targeting the membrane response to the antibiotic attack (cell membrane adaptation) as a viable strategy to increase the activity of current antimicrobials, enhance the activity of the innate immune system and prevent development of resistance during therapy using the three-component regulatory system LiaFSR of enterococci as a model.

Indexed as

Adaptation, PhysiologicalAnti-Bacterial AgentsBacillus subtilisCell MembraneDrug Resistance, Multiple, BacterialEnterococcusHumansMembrane LipidsSignal TransductionStaphylococcus aureusAnti-Bacterial AgentsLiaRS protein, Bacillus subtilisMembrane Lipids

Identifiers

PMID27458841
PMCPMC5119629

What OpenQuestion holds

Textmetadata
LicenceTDM
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.