Evidence map›Paper›PMID 37198168›Full record

ArticleScientific reports2023

Effect of cetrimonium carrier micelles on bacterial membranes and extracellular DNA, an in silico study.

Jhonatan Soto Puelles, Mahdi Ghorbani, Benjamin Tuck, Laura L Machuca, M Leigh Ackland, Fangfang Chen, Anthony E Somers, Maria Forsyth

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 37% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

8 authors at 3 institutions in 1 country.

Jhonatan Soto PuellesInstitute for Frontier Materials, Deakin University, Geelong, VIC, 3217, Australia.
Mahdi GhorbaniInstitute for Frontier Materials, Deakin University, Geelong, VIC, 3217, Australia.
Benjamin TuckCurtin Corrosion Centre, WA School of Mines: Minerals, Energy and Chemical Engineering, Curtin University, Kent Street, Bentley, WA, 6102, Australia.
Laura L MachucaCurtin Corrosion Centre, WA School of Mines: Minerals, Energy and Chemical Engineering, Curtin University, Kent Street, Bentley, WA, 6102, Australia.
M Leigh AcklandARC Centre of Excellence for Electromaterials Science (ACES), Deakin University, Burwood, 3125, Australia.
Fangfang ChenInstitute for Frontier Materials, Deakin University, Geelong, VIC, 3217, Australia. fangfang.chen@deakin.edu.au.
Anthony E SomersInstitute for Frontier Materials, Deakin University, Geelong, VIC, 3217, Australia. anthony.somers@deakin.edu.au.
Maria ForsythInstitute for Frontier Materials, Deakin University, Geelong, VIC, 3217, Australia. maria.forsyth@deakin.edu.au.
Deakin University · AUCurtin University · AUARC Centre of Excellence for Electromaterials Science · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microorganisms do not live as dispersed single cells but rather they form aggregates with extracellular polymeric substances at interfaces. Biofilms are considered efficient life forms because they shield bacteria from biocides and collect dilute nutrients. This is a big concern in industry since the microorganisms can colonize a wide range of surfaces, accelerating material deterioration, colonizing medical devices, contaminating ultrapure drinking water, increasing energy costs and creating focus of infection. Conventional biocides that target a specific component of the bacteria are not effective in the presence of biofilms. Efficient biofilm inhibitors are based on a multitarget approach interacting with the bacteria and the biofilm matrix. Their rationale design requires a thorough understanding of inhibitory mechanisms that are still largely lacking today. Herein we uncover via molecular modelling the inhibition mechanism of cetrimonium 4-OH cinnamate (CTA-4OHcinn). Simulations show that CTA-4OH micelles can disrupt symmetric and asymmetric bilayers, representative of inner and outer bacterial membranes, following three stages: adsorption, assimilation, and defect formation. The main driving force for micellar attack is electrostatic interactions. In addition to disrupting the bilayers, the micelles work as carriers facilitating the trapping of 4OH cinnamate anions within the bilayer upper leaflet and overcoming electrostatic repulsion. The micelles also interact with extracellular DNA (e-DNA), which is one of the main components of biofilms. It is observed that CTA-4OHcinn forms spherical micelles on the DNA backbone; which hinders their ability to pack. This is demonstrated by modelling the DNA along the hbb histone-like protein, showing that in the presence of CTA-4OHcinn, DNA does not pack properly around hbb. The abilities of CTA-4OHcinn to cause cell death through membrane disruption and to disperse a mature, multi-species biofilm are also confirmed experimentally.

Indexed as

DisinfectantsMicellesBacteriaBiofilmsCetrimoniumDNADNA, BacterialCetrimoniumDisinfectantsDNADNA, BacterialMicelles

Identifiers

PMID37198168
PMCPMC10192197
OpenAlexW4376958917

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.