Evidence map›Paper›PMID 36376343›Full record

ArticleScientific reports2022

Lipid-A-dependent and cholesterol-dependent dynamics properties of liposomes from gram-negative bacteria in ESKAPE.

Juan Felipe Franco-Gonzalez, Alejandra Matamoros-Recio, Angel Torres-Mozas, Blanca Rodrigo-Lacave, Sonsoles Martin-Santamaria

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 47% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Review
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

5 authors at 1 institution in 1 country.

Juan Felipe Franco-GonzalezDepartment of Structural and Chemical Biology, Centro de Investigaciones Biologicas Margarita Salas, CIB-CSIC, C/Ramiro de Maeztu, 9, 28040, Madrid, Spain. j.f.francogonzalez@gmail.com.
Alejandra Matamoros-RecioDepartment of Structural and Chemical Biology, Centro de Investigaciones Biologicas Margarita Salas, CIB-CSIC, C/Ramiro de Maeztu, 9, 28040, Madrid, Spain.
Angel Torres-MozasDepartment of Structural and Chemical Biology, Centro de Investigaciones Biologicas Margarita Salas, CIB-CSIC, C/Ramiro de Maeztu, 9, 28040, Madrid, Spain.
Blanca Rodrigo-LacaveDepartment of Structural and Chemical Biology, Centro de Investigaciones Biologicas Margarita Salas, CIB-CSIC, C/Ramiro de Maeztu, 9, 28040, Madrid, Spain.
Sonsoles Martin-SantamariaDepartment of Structural and Chemical Biology, Centro de Investigaciones Biologicas Margarita Salas, CIB-CSIC, C/Ramiro de Maeztu, 9, 28040, Madrid, Spain. smsantamaria@cib.csic.es.
Centro de Investigaciones Biológicas Margarita Salas · ES

Funding

Ministerio de Ciencia e Innovación CTQ2017-88353-RMinisterio de Ciencia e Innovación PID2020-113588RB-I00Ministerio de Ciencia y Tecnología PRE2018-086249Spanish Supercomputing Network RES-BSC QSB-2020-2-0017
6 · The paper itself

Abstract

AntiMicrobial Resistance (AMR) is a worldwide health emergency. ESKAPE pathogens include the most relevant AMR bacterial families. In particular, Gram-negative bacteria stand out due to their cell envelope complexity which exhibits strong resistance to antimicrobials. A key element for AMR is the chemical structure of lipid A, modulating the physico-chemical properties of the membrane and permeability to antibiotics. Liposomes are used as models of bacterial membrane infective vesicles. In this work, coarse-grained molecular dynamics simulations were used to model liposomes from ESKAPE Gram-negative bacteria (Escherichia coli, Klebsiella pneumoniae, Acinetobacter baumannii, and Pseudomonas aeruginosa). We captured the role of lipid A, cardiolipin and cholesterol on liposome morphology and physico-chemical properties. Additionally, the reported antimicrobial peptides Cecropin B1, JB95, and PTCDA1-kf, were used to unveil their implications on membrane disruption. This study opens a promising starting point to understand molecular keys of bacterial membranes and to promote the discovery of new antimicrobials to overcome AMR.

Indexed as

Acinetobacter baumanniiLiposomesAnti-Bacterial AgentsCholesterolEscherichia coliGram-Negative BacteriaHumansLipid AMicrobial Sensitivity TestsPseudomonas aeruginosaAnti-Bacterial AgentsCholesterolLipid ALiposomes

Identifiers

PMID36376343
PMCPMC9663605
OpenAlexW4308998316

What OpenQuestion holds

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LicenceCC BY
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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.