Potentiating activity of luteolin on membrane permeabilizing agent and ATPase inhibitor against methicillin-resistant Staphylococcus aureus

Objective:To investigate the mechanism of antibacterial activity of luteoiin(LUT) against methicillin-resistant Staphylococcus aureus(MRSA).Methods:The mechanism of anti-MRSA activity of LUT was analyzed by the viability assay in membrane permeabilizing agent ATPase inhibitors,and peptidoglycan(PGN)...

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Veröffentlicht in:Asian Pacific journal of tropical medicine 2016-01, Vol.9 (1), p.16-19
Hauptverfasser: Joung, Dae-Ki, Lee, Young-Seob, Han, Sin-Hee, Lee, Sang-Won, Cha, Seon-Woo, Mun, Su-Hyun, Kong, Ryong, Kang, Ok-Hwa, Song, Ho-Jun, Shin, Dong-Won, Kwon, Dong-Yeul
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container_issue 1
container_start_page 16
container_title Asian Pacific journal of tropical medicine
container_volume 9
creator Joung, Dae-Ki
Lee, Young-Seob
Han, Sin-Hee
Lee, Sang-Won
Cha, Seon-Woo
Mun, Su-Hyun
Kong, Ryong
Kang, Ok-Hwa
Song, Ho-Jun
Shin, Dong-Won
Kwon, Dong-Yeul
description Objective:To investigate the mechanism of antibacterial activity of luteoiin(LUT) against methicillin-resistant Staphylococcus aureus(MRSA).Methods:The mechanism of anti-MRSA activity of LUT was analyzed by the viability assay in membrane permeabilizing agent ATPase inhibitors,and peptidoglycan(PGN) derived from Staphylococcus aureus(S.aureus).Also,transmission electron microscopy was used to monitor survival characteristics and changes in S.aureus morphology.Results:Compared to the LUT alone,the optical density of suspensions treated with the combination of 125 μg/mL Tris and 230 μg/mL DCCD were reduced to 60%and 46%,respectively.PGN(15.6 μg/mL) gradually impeded the activity of LUT,and PGN(62.5 μg/mL) completely blocked the activity of LUT on S.aureus.Conclusions:Increased susceptibility to LUT with me Tris and DCCD combinations is evident in all tested MRSA isolates.The results indicate LUT synergy in increasing cytoplasmic membrane permeability and inhibiting ATPase.S.aureus PGN directly blocks the antibacterial activity of LUT,suggesting the direct binding of LUT with PGN.These findings may be validated for the development of antibacterial agent for low MRSA resistance.
doi_str_mv 10.1016/j.apjtm.2015.12.004
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Production and hosting by Elsevier B.V. All rights reserved.</rights><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c586t-436db40a1e832b899db1e662829d2f2d6b96c8058dbc4277a0477b3beedf51623</citedby><cites>FETCH-LOGICAL-c586t-436db40a1e832b899db1e662829d2f2d6b96c8058dbc4277a0477b3beedf51623</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/71792X/71792X.jpg</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.apjtm.2015.12.004$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>315,781,785,3551,27929,27930,46000</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26851780$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Joung, Dae-Ki</creatorcontrib><creatorcontrib>Lee, Young-Seob</creatorcontrib><creatorcontrib>Han, Sin-Hee</creatorcontrib><creatorcontrib>Lee, Sang-Won</creatorcontrib><creatorcontrib>Cha, Seon-Woo</creatorcontrib><creatorcontrib>Mun, Su-Hyun</creatorcontrib><creatorcontrib>Kong, Ryong</creatorcontrib><creatorcontrib>Kang, Ok-Hwa</creatorcontrib><creatorcontrib>Song, Ho-Jun</creatorcontrib><creatorcontrib>Shin, Dong-Won</creatorcontrib><creatorcontrib>Kwon, Dong-Yeul</creatorcontrib><title>Potentiating activity of luteolin on membrane permeabilizing agent and ATPase inhibitor against methicillin-resistant Staphylococcus aureus</title><title>Asian Pacific journal of tropical medicine</title><addtitle>Asian Pacific Journal of Tropical Medicine</addtitle><description>Objective:To investigate the mechanism of antibacterial activity of luteoiin(LUT) against methicillin-resistant Staphylococcus aureus(MRSA).Methods:The mechanism of anti-MRSA activity of LUT was analyzed by the viability assay in membrane permeabilizing agent ATPase inhibitors,and peptidoglycan(PGN) derived from Staphylococcus aureus(S.aureus).Also,transmission electron microscopy was used to monitor survival characteristics and changes in S.aureus morphology.Results:Compared to the LUT alone,the optical density of suspensions treated with the combination of 125 μg/mL Tris and 230 μg/mL DCCD were reduced to 60%and 46%,respectively.PGN(15.6 μg/mL) gradually impeded the activity of LUT,and PGN(62.5 μg/mL) completely blocked the activity of LUT on S.aureus.Conclusions:Increased susceptibility to LUT with me Tris and DCCD combinations is evident in all tested MRSA isolates.The results indicate LUT synergy in increasing cytoplasmic membrane permeability and inhibiting ATPase.S.aureus PGN directly blocks the antibacterial activity of LUT,suggesting the direct binding of LUT with PGN.These findings may be validated for the development of antibacterial agent for low MRSA resistance.</description><subject>agent;ATPase</subject><subject>ATPase inhibitor</subject><subject>aureus;Membrane</subject><subject>inhibitor;Peptidoglycan</subject><subject>Iuteolin;Methicillin-resistant</subject><subject>Luteolin</subject><subject>Membrane permeabilizing agent</subject><subject>Methicillin-resistant Staphylococcus aureus</subject><subject>Peptidoglycan</subject><subject>permeabilizing</subject><subject>Staphylococcus</subject><subject>Staphylococcus aureus</subject><issn>1995-7645</issn><issn>2352-4146</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqNkc1q3DAUhU1paYY0T1AoXpaCp5Isy9KiixD6B4EGmq6Ffq5nNNjSRJJTPK_Ql64mk2TbCiQt9J17dc-pqrcYrTHC7ONurfa7PK0Jwt0akzVC9EW1Im1HGoope1mtsBBd0zPanVUXKe1QWS0Rom9fV2eE8Q73HK2qPzchg89OZec3tTLZ3bu81GGoxzlDGJ2vg68nmHRUHuo9xAmUdqM7PPCboq2Vt_Xl7Y1KUDu_ddrlEMuTcj7lIs1bZ9xYKjURkktZFcnPrPbbZQwmGDOnWs0R5vSmejWoMcHF431e_fry-fbqW3P94-v3q8vrxnSc5Ya2zGqKFAbeEs2FsBoDY4QTYclALNOCGY46brWhpO8Von2vWw1ghw4z0p5XH051fys_KL-RuzBHXzrKJdplORwkFFsZwsWxAr8_wfsY7mZIWU4uGRjHYkeYk8S9QKKjxfj_QFnbo55QXtD2hJoYUoowyH10k4qLxEgeA5Y7-RCwPAYsMZEl4KJ699hg1hPYZ81TnAX4dAKg2HfvIMpkHHgD1kUwWdrg_tHg6Vvb4Dd3JeLnHlxwygkXHaKcloGPZ9m8zP0XtWjJvQ</recordid><startdate>20160101</startdate><enddate>20160101</enddate><creator>Joung, Dae-Ki</creator><creator>Lee, Young-Seob</creator><creator>Han, Sin-Hee</creator><creator>Lee, Sang-Won</creator><creator>Cha, Seon-Woo</creator><creator>Mun, Su-Hyun</creator><creator>Kong, Ryong</creator><creator>Kang, Ok-Hwa</creator><creator>Song, Ho-Jun</creator><creator>Shin, Dong-Won</creator><creator>Kwon, Dong-Yeul</creator><general>Elsevier B.V</general><general>Department of 0riental Pharmacy, College of Pharmacy and Wonkwang-0riental Medicines Research Institute, Wonkwang University, Iksan, Jeonbuk 570-749, Republic of Korea%Department of Herbal Crop Research, National Institute of Horticultural &amp; 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subjects agent
ATPase
ATPase inhibitor
aureus
Membrane
inhibitor
Peptidoglycan
Iuteolin
Methicillin-resistant
Luteolin
Membrane permeabilizing agent
Methicillin-resistant Staphylococcus aureus
Peptidoglycan
permeabilizing
Staphylococcus
Staphylococcus aureus
title Potentiating activity of luteolin on membrane permeabilizing agent and ATPase inhibitor against methicillin-resistant Staphylococcus aureus
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