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Assessment of free fatty acids and cholesteryl esters delivered in liposomes as novel class of antibiotic

BACKGROUND: Healthcare associated infections (HAI) with multidrug-resistant (MDR) bacteria continue to be a global threat, highlighting an urgent need for novel antibiotics. In this study, we assessed the potential of free fatty acids and cholesteryl esters that form part of the innate host defense...

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Autores principales: Cheung Lam, Annie H., Sandoval, Natalie, Wadhwa, Ritambhara, Gilkes, Janine, Do, Thai Q., Ernst, William, Chiang, Su-Ming, Kosina, Suzanne, Howard Xu, H., Fujii, Gary, Porter, Edith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4938966/
https://www.ncbi.nlm.nih.gov/pubmed/27391402
http://dx.doi.org/10.1186/s13104-016-2138-8
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author Cheung Lam, Annie H.
Sandoval, Natalie
Wadhwa, Ritambhara
Gilkes, Janine
Do, Thai Q.
Ernst, William
Chiang, Su-Ming
Kosina, Suzanne
Howard Xu, H.
Fujii, Gary
Porter, Edith
author_facet Cheung Lam, Annie H.
Sandoval, Natalie
Wadhwa, Ritambhara
Gilkes, Janine
Do, Thai Q.
Ernst, William
Chiang, Su-Ming
Kosina, Suzanne
Howard Xu, H.
Fujii, Gary
Porter, Edith
author_sort Cheung Lam, Annie H.
collection PubMed
description BACKGROUND: Healthcare associated infections (HAI) with multidrug-resistant (MDR) bacteria continue to be a global threat, highlighting an urgent need for novel antibiotics. In this study, we assessed the potential of free fatty acids and cholesteryl esters that form part of the innate host defense as novel antibacterial agents for use against MDR bacteria. METHODS: Liposomes of six different phospholipid mixtures were employed as carrier for six different fatty acids and four different cholesteryl esters. Using a modified MIC assay based on DNA quantification with the fluoroprobe Syto9, formulations were tested against Gram-positive and Gram-negative bacteria implicated in HAI. Formulations with MIC values in the low μg/mL range were further subjected to determination of minimal bactericidal activity, hemolysis assay with sheep erythrocytes, and cytotoxicity testing with the human liver cell line HepG2. The potential for synergistic activity with a standard antibiotic was also probed. RESULTS: Palmitic acid and stearic acid prepared in carrier 4 (PA4 and SA4, respectively) were identified as most active lipids (MIC against MDR Staphylococcus epidermidis was 0.5 and 0.25 μg/mL, respectively; MIC against vancomycin resistant Enterococcus faecalis (VRE) was 2 and 0.5 μg/mL, respectively). Cholesteryl linoleate formulated with carrier 3 (CL3) exhibited activity against the S. epidermidis strain (MIC 1 μg/mL) and a Pseudomonas aeruginosa strain (MIC 8 μg/mL) and lowered the vancomycin MIC for VRE from 32–64 μg/mL to as low as 4 μg/mL. At 90 μg/mL PA4, SA4, and CL3 effected less than 5 % hemolysis over 3 h and PA4 and CL3 did not exhibit significant cytotoxic activity against HepG2 cells when applied at 100 μg/mL over 48 h. CONCLUSIONS: Our results showed that selected fatty acids and cholesteryl esters packaged with phospholipids exhibit antibacterial activity against Gram-positive and Gram-negative bacteria and may augment the activity of antibiotics. Bactericidal activity could be unlinked from hemolytic and cytotoxic activity and the type of phospholipid carrier greatly influenced the activity. Thus, fatty acids and cholesteryl esters packaged in liposomes may have potential as novel lipophilic antimicrobial agents. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13104-016-2138-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-49389662016-07-10 Assessment of free fatty acids and cholesteryl esters delivered in liposomes as novel class of antibiotic Cheung Lam, Annie H. Sandoval, Natalie Wadhwa, Ritambhara Gilkes, Janine Do, Thai Q. Ernst, William Chiang, Su-Ming Kosina, Suzanne Howard Xu, H. Fujii, Gary Porter, Edith BMC Res Notes Research Article BACKGROUND: Healthcare associated infections (HAI) with multidrug-resistant (MDR) bacteria continue to be a global threat, highlighting an urgent need for novel antibiotics. In this study, we assessed the potential of free fatty acids and cholesteryl esters that form part of the innate host defense as novel antibacterial agents for use against MDR bacteria. METHODS: Liposomes of six different phospholipid mixtures were employed as carrier for six different fatty acids and four different cholesteryl esters. Using a modified MIC assay based on DNA quantification with the fluoroprobe Syto9, formulations were tested against Gram-positive and Gram-negative bacteria implicated in HAI. Formulations with MIC values in the low μg/mL range were further subjected to determination of minimal bactericidal activity, hemolysis assay with sheep erythrocytes, and cytotoxicity testing with the human liver cell line HepG2. The potential for synergistic activity with a standard antibiotic was also probed. RESULTS: Palmitic acid and stearic acid prepared in carrier 4 (PA4 and SA4, respectively) were identified as most active lipids (MIC against MDR Staphylococcus epidermidis was 0.5 and 0.25 μg/mL, respectively; MIC against vancomycin resistant Enterococcus faecalis (VRE) was 2 and 0.5 μg/mL, respectively). Cholesteryl linoleate formulated with carrier 3 (CL3) exhibited activity against the S. epidermidis strain (MIC 1 μg/mL) and a Pseudomonas aeruginosa strain (MIC 8 μg/mL) and lowered the vancomycin MIC for VRE from 32–64 μg/mL to as low as 4 μg/mL. At 90 μg/mL PA4, SA4, and CL3 effected less than 5 % hemolysis over 3 h and PA4 and CL3 did not exhibit significant cytotoxic activity against HepG2 cells when applied at 100 μg/mL over 48 h. CONCLUSIONS: Our results showed that selected fatty acids and cholesteryl esters packaged with phospholipids exhibit antibacterial activity against Gram-positive and Gram-negative bacteria and may augment the activity of antibiotics. Bactericidal activity could be unlinked from hemolytic and cytotoxic activity and the type of phospholipid carrier greatly influenced the activity. Thus, fatty acids and cholesteryl esters packaged in liposomes may have potential as novel lipophilic antimicrobial agents. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13104-016-2138-8) contains supplementary material, which is available to authorized users. BioMed Central 2016-07-08 /pmc/articles/PMC4938966/ /pubmed/27391402 http://dx.doi.org/10.1186/s13104-016-2138-8 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Cheung Lam, Annie H.
Sandoval, Natalie
Wadhwa, Ritambhara
Gilkes, Janine
Do, Thai Q.
Ernst, William
Chiang, Su-Ming
Kosina, Suzanne
Howard Xu, H.
Fujii, Gary
Porter, Edith
Assessment of free fatty acids and cholesteryl esters delivered in liposomes as novel class of antibiotic
title Assessment of free fatty acids and cholesteryl esters delivered in liposomes as novel class of antibiotic
title_full Assessment of free fatty acids and cholesteryl esters delivered in liposomes as novel class of antibiotic
title_fullStr Assessment of free fatty acids and cholesteryl esters delivered in liposomes as novel class of antibiotic
title_full_unstemmed Assessment of free fatty acids and cholesteryl esters delivered in liposomes as novel class of antibiotic
title_short Assessment of free fatty acids and cholesteryl esters delivered in liposomes as novel class of antibiotic
title_sort assessment of free fatty acids and cholesteryl esters delivered in liposomes as novel class of antibiotic
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4938966/
https://www.ncbi.nlm.nih.gov/pubmed/27391402
http://dx.doi.org/10.1186/s13104-016-2138-8
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