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

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 th...

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Autores principales: Puelles, Jhonatan Soto, Ghorbani, Mahdi, Tuck, Benjamin, Machuca, Laura L., Ackland, M. Leigh, Chen, Fangfang, Somers, Anthony E., Forsyth, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10192197/
https://www.ncbi.nlm.nih.gov/pubmed/37198168
http://dx.doi.org/10.1038/s41598-023-32475-x
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author Puelles, Jhonatan Soto
Ghorbani, Mahdi
Tuck, Benjamin
Machuca, Laura L.
Ackland, M. Leigh
Chen, Fangfang
Somers, Anthony E.
Forsyth, Maria
author_facet Puelles, Jhonatan Soto
Ghorbani, Mahdi
Tuck, Benjamin
Machuca, Laura L.
Ackland, M. Leigh
Chen, Fangfang
Somers, Anthony E.
Forsyth, Maria
author_sort Puelles, Jhonatan Soto
collection PubMed
description 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.
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spelling pubmed-101921972023-05-19 Effect of cetrimonium carrier micelles on bacterial membranes and extracellular DNA, an in silico study Puelles, Jhonatan Soto Ghorbani, Mahdi Tuck, Benjamin Machuca, Laura L. Ackland, M. Leigh Chen, Fangfang Somers, Anthony E. Forsyth, Maria Sci Rep Article 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. Nature Publishing Group UK 2023-05-17 /pmc/articles/PMC10192197/ /pubmed/37198168 http://dx.doi.org/10.1038/s41598-023-32475-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Puelles, Jhonatan Soto
Ghorbani, Mahdi
Tuck, Benjamin
Machuca, Laura L.
Ackland, M. Leigh
Chen, Fangfang
Somers, Anthony E.
Forsyth, Maria
Effect of cetrimonium carrier micelles on bacterial membranes and extracellular DNA, an in silico study
title Effect of cetrimonium carrier micelles on bacterial membranes and extracellular DNA, an in silico study
title_full Effect of cetrimonium carrier micelles on bacterial membranes and extracellular DNA, an in silico study
title_fullStr Effect of cetrimonium carrier micelles on bacterial membranes and extracellular DNA, an in silico study
title_full_unstemmed Effect of cetrimonium carrier micelles on bacterial membranes and extracellular DNA, an in silico study
title_short Effect of cetrimonium carrier micelles on bacterial membranes and extracellular DNA, an in silico study
title_sort effect of cetrimonium carrier micelles on bacterial membranes and extracellular dna, an in silico study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10192197/
https://www.ncbi.nlm.nih.gov/pubmed/37198168
http://dx.doi.org/10.1038/s41598-023-32475-x
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