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Antibacterial effect, efflux pump inhibitory (NorA, TetK and MepA) of Staphylococcus aureus and in silico prediction of α, β and δ-damascone compounds
The present study aimed to evaluate the antibacterial effect and inhibitory capacity against NorA, TetK and MepA efflux pump of Staphylococcus aureus multiresistant by in vitro and in silico approach of α, β and δ-damascone compounds. The compounds α, β and δ-damascone showed a clinically relevant e...
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Published in: | Arabian journal of chemistry 2023-02, Vol.16 (2), p.104482, Article 104482 |
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creator | Rayane Correia de Oliveira, Maria Gabriely de Lima Silva, Maria Datiane de Morais Oliveira-Tintino, Cícera Relison Tintino, Saulo Esmeraldo Rocha, Janaina Ernani Alves Magalhães, Francisco Henrique Sousa da Costa, Roger Torres Pessoa, Renata Sousa Alcântara, Isabel Oliveira Brito Pereira Bezerra Martins, Anita Douglas Melo Coutinho, Henrique Raposo, António Carrascosa, Conrado Raduan Jaber, José Aquino Saraiva, Rogério Rose Alencar de Menezes, Irwin |
description | The present study aimed to evaluate the antibacterial effect and inhibitory capacity against NorA, TetK and MepA efflux pump of Staphylococcus aureus multiresistant by in vitro and in silico approach of α, β and δ-damascone compounds.
The compounds α, β and δ-damascone showed a clinically relevant effect against S. aureus ATCC 6538 standard strain. A modulating effect was also observed in association with antibiotics against MDR strains. Regarding the inhibition of the efflux pump, the compounds showed a modulating effect with antibiotics, against SA-1199, SA-1199B, SA IS-58 and K2068. Only δ-damascone demonstrated an efflux pump inhibitory effect. Regarding ADME properties, α, β and δ-damascone showed similar physicochemical properties with good pharmacokinetic characteristics, such as lipophilicity, oral bioavailability and low toxicity. In addition, they exhibited the binding energy and Ligand Efficiency (LE) −81.17 (5.4), −77.48(-5.4) and −64.55 (-5.1), which shows good interactions with the critical residues of the MepA receptor.
From the results it is concluded that the compounds α, β and δ-damascone do not have antibacterial activity, but show a modulating effect in association with antibiotics, as well as not showing direct activity on the efflux pump, but they do have a modulating effect with antibiotics and with EtBr (α and β-damascone). |
doi_str_mv | 10.1016/j.arabjc.2022.104482 |
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The compounds α, β and δ-damascone showed a clinically relevant effect against S. aureus ATCC 6538 standard strain. A modulating effect was also observed in association with antibiotics against MDR strains. Regarding the inhibition of the efflux pump, the compounds showed a modulating effect with antibiotics, against SA-1199, SA-1199B, SA IS-58 and K2068. Only δ-damascone demonstrated an efflux pump inhibitory effect. Regarding ADME properties, α, β and δ-damascone showed similar physicochemical properties with good pharmacokinetic characteristics, such as lipophilicity, oral bioavailability and low toxicity. In addition, they exhibited the binding energy and Ligand Efficiency (LE) −81.17 (5.4), −77.48(-5.4) and −64.55 (-5.1), which shows good interactions with the critical residues of the MepA receptor.
From the results it is concluded that the compounds α, β and δ-damascone do not have antibacterial activity, but show a modulating effect in association with antibiotics, as well as not showing direct activity on the efflux pump, but they do have a modulating effect with antibiotics and with EtBr (α and β-damascone).</description><identifier>ISSN: 1878-5352</identifier><identifier>EISSN: 1878-5379</identifier><identifier>DOI: 10.1016/j.arabjc.2022.104482</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>ADME ; Antibacterial ; Damascone ; Efflux pump ; Molecular docking</subject><ispartof>Arabian journal of chemistry, 2023-02, Vol.16 (2), p.104482, Article 104482</ispartof><rights>2022 The Authors</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3332-5973ea07c2ec0db007b1700127ded3fa0003b6ed5e2d7c557cdbefaa9d193b723</citedby><cites>FETCH-LOGICAL-c3332-5973ea07c2ec0db007b1700127ded3fa0003b6ed5e2d7c557cdbefaa9d193b723</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1878535222007985$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3549,27924,27925,45780</link.rule.ids></links><search><creatorcontrib>Rayane Correia de Oliveira, Maria</creatorcontrib><creatorcontrib>Gabriely de Lima Silva, Maria</creatorcontrib><creatorcontrib>Datiane de Morais Oliveira-Tintino, Cícera</creatorcontrib><creatorcontrib>Relison Tintino, Saulo</creatorcontrib><creatorcontrib>Esmeraldo Rocha, Janaina</creatorcontrib><creatorcontrib>Ernani Alves Magalhães, Francisco</creatorcontrib><creatorcontrib>Henrique Sousa da Costa, Roger</creatorcontrib><creatorcontrib>Torres Pessoa, Renata</creatorcontrib><creatorcontrib>Sousa Alcântara, Isabel</creatorcontrib><creatorcontrib>Oliveira Brito Pereira Bezerra Martins, Anita</creatorcontrib><creatorcontrib>Douglas Melo Coutinho, Henrique</creatorcontrib><creatorcontrib>Raposo, António</creatorcontrib><creatorcontrib>Carrascosa, Conrado</creatorcontrib><creatorcontrib>Raduan Jaber, José</creatorcontrib><creatorcontrib>Aquino Saraiva, Rogério</creatorcontrib><creatorcontrib>Rose Alencar de Menezes, Irwin</creatorcontrib><title>Antibacterial effect, efflux pump inhibitory (NorA, TetK and MepA) of Staphylococcus aureus and in silico prediction of α, β and δ-damascone compounds</title><title>Arabian journal of chemistry</title><description>The present study aimed to evaluate the antibacterial effect and inhibitory capacity against NorA, TetK and MepA efflux pump of Staphylococcus aureus multiresistant by in vitro and in silico approach of α, β and δ-damascone compounds.
The compounds α, β and δ-damascone showed a clinically relevant effect against S. aureus ATCC 6538 standard strain. A modulating effect was also observed in association with antibiotics against MDR strains. Regarding the inhibition of the efflux pump, the compounds showed a modulating effect with antibiotics, against SA-1199, SA-1199B, SA IS-58 and K2068. Only δ-damascone demonstrated an efflux pump inhibitory effect. Regarding ADME properties, α, β and δ-damascone showed similar physicochemical properties with good pharmacokinetic characteristics, such as lipophilicity, oral bioavailability and low toxicity. In addition, they exhibited the binding energy and Ligand Efficiency (LE) −81.17 (5.4), −77.48(-5.4) and −64.55 (-5.1), which shows good interactions with the critical residues of the MepA receptor.
From the results it is concluded that the compounds α, β and δ-damascone do not have antibacterial activity, but show a modulating effect in association with antibiotics, as well as not showing direct activity on the efflux pump, but they do have a modulating effect with antibiotics and with EtBr (α and β-damascone).</description><subject>ADME</subject><subject>Antibacterial</subject><subject>Damascone</subject><subject>Efflux pump</subject><subject>Molecular docking</subject><issn>1878-5352</issn><issn>1878-5379</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9kc1u1DAUhSMEEqXwBiy8BGky-Ce_G6RRBaWiwIKytq6vb6hHmTiyE8Q8Co9BxXPMM-E0qEtWx76655OPT5a9FHwruKje7LcQwOxxK7mUaVQUjXyUnYmmbvJS1e3jh3Mpn2bPYtxzXnOuqrPs126YnAGcKDjoGXUd4bRZtJ9_snE-jMwNt864yYcje_XZh92G3dD0kcFg2Scad6-Z79jXCcbbY-_RI86RwRxokbTiBhZd79CzMZB1ODk_LI7T7w073d2vnP7kFg4Q0Q_E0B9GPw82Ps-edNBHevFPz7Nv79_dXHzIr79cXl3srnNUSsm8bGtFwGuUhNyaFMyIlE3I2pJVHfCU01RkS5K2xrKs0RrqAForWmVqqc6zq5VrPez1GNwBwlF7cPp-4MN3DWFy2JOGBkvkqpWNgUKoqimLphO2JWOrdFWJVawsDD7GQN0DT3C9VKX3eq1KL1Xptapke7vaKOX84SjoiI4GTP8VUh3pIe7_gL9ToKHI</recordid><startdate>202302</startdate><enddate>202302</enddate><creator>Rayane Correia de Oliveira, Maria</creator><creator>Gabriely de Lima Silva, Maria</creator><creator>Datiane de Morais Oliveira-Tintino, Cícera</creator><creator>Relison Tintino, Saulo</creator><creator>Esmeraldo Rocha, Janaina</creator><creator>Ernani Alves Magalhães, Francisco</creator><creator>Henrique Sousa da Costa, Roger</creator><creator>Torres Pessoa, Renata</creator><creator>Sousa Alcântara, Isabel</creator><creator>Oliveira Brito Pereira Bezerra Martins, Anita</creator><creator>Douglas Melo Coutinho, Henrique</creator><creator>Raposo, António</creator><creator>Carrascosa, Conrado</creator><creator>Raduan Jaber, José</creator><creator>Aquino Saraiva, Rogério</creator><creator>Rose Alencar de Menezes, Irwin</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>DOA</scope></search><sort><creationdate>202302</creationdate><title>Antibacterial effect, efflux pump inhibitory (NorA, TetK and MepA) of Staphylococcus aureus and in silico prediction of α, β and δ-damascone compounds</title><author>Rayane Correia de Oliveira, Maria ; 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The compounds α, β and δ-damascone showed a clinically relevant effect against S. aureus ATCC 6538 standard strain. A modulating effect was also observed in association with antibiotics against MDR strains. Regarding the inhibition of the efflux pump, the compounds showed a modulating effect with antibiotics, against SA-1199, SA-1199B, SA IS-58 and K2068. Only δ-damascone demonstrated an efflux pump inhibitory effect. Regarding ADME properties, α, β and δ-damascone showed similar physicochemical properties with good pharmacokinetic characteristics, such as lipophilicity, oral bioavailability and low toxicity. In addition, they exhibited the binding energy and Ligand Efficiency (LE) −81.17 (5.4), −77.48(-5.4) and −64.55 (-5.1), which shows good interactions with the critical residues of the MepA receptor.
From the results it is concluded that the compounds α, β and δ-damascone do not have antibacterial activity, but show a modulating effect in association with antibiotics, as well as not showing direct activity on the efflux pump, but they do have a modulating effect with antibiotics and with EtBr (α and β-damascone).</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.arabjc.2022.104482</doi><oa>free_for_read</oa></addata></record> |
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subjects | ADME Antibacterial Damascone Efflux pump Molecular docking |
title | Antibacterial effect, efflux pump inhibitory (NorA, TetK and MepA) of Staphylococcus aureus and in silico prediction of α, β and δ-damascone compounds |
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