<i>Eisenia bicyclis</i>-Mediated Gold Nanoparticles Exhibit Antibiofilm and Antivirulence Activities Against <i>Pseudomonas aeruginosa</i> and <i>Staphylococcus aureus</i>

<b>Background/Objectives:</b> Brown algae, particularly <i>Eisenia bicyclis</i>, produce various bioactive chemicals with significant application potential in the food, cosmetics, and pharmaceutical industries. This study aimed to evaluate the antibacterial, antibiofilm, and...

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Main Authors: Do Kyung Oh, Du-Min Jo, Nam-Gyun Kim, Kyung-Jin Cho, Geum-Jae Jeong, Nazia Tabassum, Won-Kyo Jung, Fazlurrahman Khan, Young-Mog Kim
Format: Article
Language:English
Published: MDPI AG 2025-02-01
Series:Antibiotics
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Online Access:https://www.mdpi.com/2079-6382/14/2/182
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author Do Kyung Oh
Du-Min Jo
Nam-Gyun Kim
Kyung-Jin Cho
Geum-Jae Jeong
Nazia Tabassum
Won-Kyo Jung
Fazlurrahman Khan
Young-Mog Kim
author_facet Do Kyung Oh
Du-Min Jo
Nam-Gyun Kim
Kyung-Jin Cho
Geum-Jae Jeong
Nazia Tabassum
Won-Kyo Jung
Fazlurrahman Khan
Young-Mog Kim
author_sort Do Kyung Oh
collection DOAJ
description <b>Background/Objectives:</b> Brown algae, particularly <i>Eisenia bicyclis</i>, produce various bioactive chemicals with significant application potential in the food, cosmetics, and pharmaceutical industries. This study aimed to evaluate the antibacterial, antibiofilm, and antivirulence properties of the ethyl acetate fraction (EA) of <i>E. bicyclis</i> and its synthesized gold nanoparticles (EA-AuNPs), with a focus on their potential applications against both Gram-positive and Gram-negative bacteria. <b>Methods:</b> The bioactive component in the ethyl acetate fraction was identified using a gas chromatography-mass spectroscopy (GC-MS) device and a liquid chromatography-mass spectrometer/mass spectrometry (LC-MS) system. The crystal violet method was utilized to evaluate the biofilm inhibition experiments. Several instruments, including dynamic light scattering, Fourier transform infrared, X-ray diffraction, field emission transmission electron microscopy, and energy-dispersive spectroscopy, were employed to completely characterize the produced EA-AuNPs. The cytotoxicity of the EA-AuNPs was determined using the MTT assay, and the expression of genes linked with biofilm and virulence in <i>Pseudomonas aeruginosa</i> and <i>Staphylococcus aureus</i> was investigated using real-time polymerase chain reaction (RT-PCR). <b>Results:</b> Various bioactive compounds were identified from the EA using GC-MS and LC-MS, including fatty acids and phlorotannins such as eckol, dieckol, 6,6’-bieckol, and phlorofucofuroeckol in high amounts, highlighting EA as a phlorotannin-rich fraction. The EA also demonstrated significant antibiofilm activity, with 79.86% inhibition at 512 μg/mL against <i>P. aeruginosa</i> and 87.00% at 64 μg/mL against <i>S. aureus</i>. EA was then used in the synthesis of gold nanoparticles (AuNPs) to improve their stability and safety. The synthesized EA-AuNPs were determined to have an average size of 165.04 nm, with a zeta potential of −29.86 mV, indicating good stability. In antibiofilm activity assays, EA-AuNPs demonstrated 45.76% inhibition against <i>P. aeruginosa</i> at 1024 μg/mL and 44.64% inhibition against <i>S. aureus</i> at 128 μg/mL. At sub-MIC levels, EA-AuNPs significantly inhibited biofilm formation and virulence factors, including the motility of <i>P. aeruginosa</i> and staphyloxanthin synthesis in <i>S. aureus</i>. The RT-PCR analysis revealed the downregulation of key genes involved in biofilm formation and virulence in <i>P. aeruginosa</i> and <i>S. aureus</i>. <b>Conclusions:</b> These findings highlight the potential of <i>E. bicyclis</i> solvent-soluble extracts and EA-AuNPs as effective antibacterial, antibiofilm, and antivirulence agents, with significant application potential in the pharmaceutical and food industries. To the best of our knowledge, this is the first report of antibiofilm activity against both Gram-positive and Gram-negative bacteria using EA-AuNPs.
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spelling doaj-art-6d2a98ca8d3b4387bcf2564c19e8aea92025-08-20T03:11:19ZengMDPI AGAntibiotics2079-63822025-02-0114218210.3390/antibiotics14020182<i>Eisenia bicyclis</i>-Mediated Gold Nanoparticles Exhibit Antibiofilm and Antivirulence Activities Against <i>Pseudomonas aeruginosa</i> and <i>Staphylococcus aureus</i>Do Kyung Oh0Du-Min Jo1Nam-Gyun Kim2Kyung-Jin Cho3Geum-Jae Jeong4Nazia Tabassum5Won-Kyo Jung6Fazlurrahman Khan7Young-Mog Kim8Department of Food Science and Technology, Pukyong National University, Busan 48513, Republic of KoreaNational Marine Biodiversity of Korea (MABIK), Seochun 33662, Republic of KoreaMarine Integrated Biomedical Technology Center, The National Key Research Institutes in Universities, Pukyong National University, Busan 48513, Republic of KoreaDepartment of Food Science and Technology, Pukyong National University, Busan 48513, Republic of KoreaDepartment of Food Science and Technology, Pukyong National University, Busan 48513, Republic of KoreaMarine Integrated Biomedical Technology Center, The National Key Research Institutes in Universities, Pukyong National University, Busan 48513, Republic of KoreaMarine Integrated Biomedical Technology Center, The National Key Research Institutes in Universities, Pukyong National University, Busan 48513, Republic of KoreaMarine Integrated Biomedical Technology Center, The National Key Research Institutes in Universities, Pukyong National University, Busan 48513, Republic of KoreaDepartment of Food Science and Technology, Pukyong National University, Busan 48513, Republic of Korea<b>Background/Objectives:</b> Brown algae, particularly <i>Eisenia bicyclis</i>, produce various bioactive chemicals with significant application potential in the food, cosmetics, and pharmaceutical industries. This study aimed to evaluate the antibacterial, antibiofilm, and antivirulence properties of the ethyl acetate fraction (EA) of <i>E. bicyclis</i> and its synthesized gold nanoparticles (EA-AuNPs), with a focus on their potential applications against both Gram-positive and Gram-negative bacteria. <b>Methods:</b> The bioactive component in the ethyl acetate fraction was identified using a gas chromatography-mass spectroscopy (GC-MS) device and a liquid chromatography-mass spectrometer/mass spectrometry (LC-MS) system. The crystal violet method was utilized to evaluate the biofilm inhibition experiments. Several instruments, including dynamic light scattering, Fourier transform infrared, X-ray diffraction, field emission transmission electron microscopy, and energy-dispersive spectroscopy, were employed to completely characterize the produced EA-AuNPs. The cytotoxicity of the EA-AuNPs was determined using the MTT assay, and the expression of genes linked with biofilm and virulence in <i>Pseudomonas aeruginosa</i> and <i>Staphylococcus aureus</i> was investigated using real-time polymerase chain reaction (RT-PCR). <b>Results:</b> Various bioactive compounds were identified from the EA using GC-MS and LC-MS, including fatty acids and phlorotannins such as eckol, dieckol, 6,6’-bieckol, and phlorofucofuroeckol in high amounts, highlighting EA as a phlorotannin-rich fraction. The EA also demonstrated significant antibiofilm activity, with 79.86% inhibition at 512 μg/mL against <i>P. aeruginosa</i> and 87.00% at 64 μg/mL against <i>S. aureus</i>. EA was then used in the synthesis of gold nanoparticles (AuNPs) to improve their stability and safety. The synthesized EA-AuNPs were determined to have an average size of 165.04 nm, with a zeta potential of −29.86 mV, indicating good stability. In antibiofilm activity assays, EA-AuNPs demonstrated 45.76% inhibition against <i>P. aeruginosa</i> at 1024 μg/mL and 44.64% inhibition against <i>S. aureus</i> at 128 μg/mL. At sub-MIC levels, EA-AuNPs significantly inhibited biofilm formation and virulence factors, including the motility of <i>P. aeruginosa</i> and staphyloxanthin synthesis in <i>S. aureus</i>. The RT-PCR analysis revealed the downregulation of key genes involved in biofilm formation and virulence in <i>P. aeruginosa</i> and <i>S. aureus</i>. <b>Conclusions:</b> These findings highlight the potential of <i>E. bicyclis</i> solvent-soluble extracts and EA-AuNPs as effective antibacterial, antibiofilm, and antivirulence agents, with significant application potential in the pharmaceutical and food industries. To the best of our knowledge, this is the first report of antibiofilm activity against both Gram-positive and Gram-negative bacteria using EA-AuNPs.https://www.mdpi.com/2079-6382/14/2/182<i>Eisenia bicyclis</i>gold nanoparticlesantibiofilmantivirulencesecondary metabolitesgene expression
spellingShingle Do Kyung Oh
Du-Min Jo
Nam-Gyun Kim
Kyung-Jin Cho
Geum-Jae Jeong
Nazia Tabassum
Won-Kyo Jung
Fazlurrahman Khan
Young-Mog Kim
<i>Eisenia bicyclis</i>-Mediated Gold Nanoparticles Exhibit Antibiofilm and Antivirulence Activities Against <i>Pseudomonas aeruginosa</i> and <i>Staphylococcus aureus</i>
Antibiotics
<i>Eisenia bicyclis</i>
gold nanoparticles
antibiofilm
antivirulence
secondary metabolites
gene expression
title <i>Eisenia bicyclis</i>-Mediated Gold Nanoparticles Exhibit Antibiofilm and Antivirulence Activities Against <i>Pseudomonas aeruginosa</i> and <i>Staphylococcus aureus</i>
title_full <i>Eisenia bicyclis</i>-Mediated Gold Nanoparticles Exhibit Antibiofilm and Antivirulence Activities Against <i>Pseudomonas aeruginosa</i> and <i>Staphylococcus aureus</i>
title_fullStr <i>Eisenia bicyclis</i>-Mediated Gold Nanoparticles Exhibit Antibiofilm and Antivirulence Activities Against <i>Pseudomonas aeruginosa</i> and <i>Staphylococcus aureus</i>
title_full_unstemmed <i>Eisenia bicyclis</i>-Mediated Gold Nanoparticles Exhibit Antibiofilm and Antivirulence Activities Against <i>Pseudomonas aeruginosa</i> and <i>Staphylococcus aureus</i>
title_short <i>Eisenia bicyclis</i>-Mediated Gold Nanoparticles Exhibit Antibiofilm and Antivirulence Activities Against <i>Pseudomonas aeruginosa</i> and <i>Staphylococcus aureus</i>
title_sort i eisenia bicyclis i mediated gold nanoparticles exhibit antibiofilm and antivirulence activities against i pseudomonas aeruginosa i and i staphylococcus aureus i
topic <i>Eisenia bicyclis</i>
gold nanoparticles
antibiofilm
antivirulence
secondary metabolites
gene expression
url https://www.mdpi.com/2079-6382/14/2/182
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