Antibacterial Activity and Untargeted Metabolomics Profiling of IAcalypha arvensis/I Poepp
The search for potent antimicrobial compounds is critical in the face of growing antibiotic resistance. This study explores Acalypha arvensis Poepp. (A. arvensis), a Caribbean plant traditionally used for disease treatment. The dried plant powder was subjected to successive extractions using differe...
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creator | Thesnor, Valendy Molinié, Roland Giebelhaus, Ryland T de la Mata Espinosa, A. Paulina Harynuk, James J Bénimélis, David Vanhoye, Bérénice Dunyach-Rémy, Catherine Sylvestre, Muriel Cheremond, Yvens Meffre, Patrick Cebrián-Torrejón, Gerardo Benfodda, Zohra |
description | The search for potent antimicrobial compounds is critical in the face of growing antibiotic resistance. This study explores Acalypha arvensis Poepp. (A. arvensis), a Caribbean plant traditionally used for disease treatment. The dried plant powder was subjected to successive extractions using different solvents: hexane (F1), dichloromethane (F2), methanol (F3), a 50:50 mixture of methanol and water (F4), and water (F5). Additionally, a parallel extraction was conducted using a 50:50 mixture of methanol and chloroform (F6). All the fractions were evaluated for their antimicrobial activity, and the F6 fraction was characterized using untargeted metabolomics using SPME-GC×GC-TOFMS. The extracts of A. arvensis F3, F4, and F5 showed antibacterial activity against Staphylococcus aureus ATCC 25923 (5 mg/mL), MRSA BA22038 (5 mg/mL), and Pseudomonas aeruginosa ATCC 27853 (10 mg/mL), and fraction F6 showed antibacterial activity against Staphylococcus aureus ATCC 29213 (2 mg/mL), Escherichia coli ATCC 25922 (20 mg/mL), Pseudomonas aeruginosa ATCC 27853 (10 mg/mL), Enterococcus faecalis ATCC 29212 (10 mg/mL), Staphylococcus aureus 024 (2 mg/mL), and Staphylococcus aureus 003 (2 mg/mL). Metabolomic analysis of F6 revealed 2861 peaks with 58 identified compounds through SPME and 3654 peaks with 29 identified compounds through derivatization. The compounds included methyl ester fatty acids, ethyl ester fatty acids, terpenes, ketones, sugars, amino acids, and fatty acids. This study represents the first exploration of A. arvensis metabolomics and its antimicrobial potential, providing valuable insights for plant classification, phytochemical research, and drug discovery. |
doi_str_mv | 10.3390/molecules28237882 |
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Paulina ; Harynuk, James J ; Bénimélis, David ; Vanhoye, Bérénice ; Dunyach-Rémy, Catherine ; Sylvestre, Muriel ; Cheremond, Yvens ; Meffre, Patrick ; Cebrián-Torrejón, Gerardo ; Benfodda, Zohra</creator><creatorcontrib>Thesnor, Valendy ; Molinié, Roland ; Giebelhaus, Ryland T ; de la Mata Espinosa, A. Paulina ; Harynuk, James J ; Bénimélis, David ; Vanhoye, Bérénice ; Dunyach-Rémy, Catherine ; Sylvestre, Muriel ; Cheremond, Yvens ; Meffre, Patrick ; Cebrián-Torrejón, Gerardo ; Benfodda, Zohra</creatorcontrib><description>The search for potent antimicrobial compounds is critical in the face of growing antibiotic resistance. This study explores Acalypha arvensis Poepp. (A. arvensis), a Caribbean plant traditionally used for disease treatment. The dried plant powder was subjected to successive extractions using different solvents: hexane (F1), dichloromethane (F2), methanol (F3), a 50:50 mixture of methanol and water (F4), and water (F5). Additionally, a parallel extraction was conducted using a 50:50 mixture of methanol and chloroform (F6). All the fractions were evaluated for their antimicrobial activity, and the F6 fraction was characterized using untargeted metabolomics using SPME-GC×GC-TOFMS. The extracts of A. arvensis F3, F4, and F5 showed antibacterial activity against Staphylococcus aureus ATCC 25923 (5 mg/mL), MRSA BA22038 (5 mg/mL), and Pseudomonas aeruginosa ATCC 27853 (10 mg/mL), and fraction F6 showed antibacterial activity against Staphylococcus aureus ATCC 29213 (2 mg/mL), Escherichia coli ATCC 25922 (20 mg/mL), Pseudomonas aeruginosa ATCC 27853 (10 mg/mL), Enterococcus faecalis ATCC 29212 (10 mg/mL), Staphylococcus aureus 024 (2 mg/mL), and Staphylococcus aureus 003 (2 mg/mL). Metabolomic analysis of F6 revealed 2861 peaks with 58 identified compounds through SPME and 3654 peaks with 29 identified compounds through derivatization. The compounds included methyl ester fatty acids, ethyl ester fatty acids, terpenes, ketones, sugars, amino acids, and fatty acids. 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Paulina</creatorcontrib><creatorcontrib>Harynuk, James J</creatorcontrib><creatorcontrib>Bénimélis, David</creatorcontrib><creatorcontrib>Vanhoye, Bérénice</creatorcontrib><creatorcontrib>Dunyach-Rémy, Catherine</creatorcontrib><creatorcontrib>Sylvestre, Muriel</creatorcontrib><creatorcontrib>Cheremond, Yvens</creatorcontrib><creatorcontrib>Meffre, Patrick</creatorcontrib><creatorcontrib>Cebrián-Torrejón, Gerardo</creatorcontrib><creatorcontrib>Benfodda, Zohra</creatorcontrib><title>Antibacterial Activity and Untargeted Metabolomics Profiling of IAcalypha arvensis/I Poepp</title><title>Molecules (Basel, Switzerland)</title><description>The search for potent antimicrobial compounds is critical in the face of growing antibiotic resistance. This study explores Acalypha arvensis Poepp. (A. arvensis), a Caribbean plant traditionally used for disease treatment. The dried plant powder was subjected to successive extractions using different solvents: hexane (F1), dichloromethane (F2), methanol (F3), a 50:50 mixture of methanol and water (F4), and water (F5). Additionally, a parallel extraction was conducted using a 50:50 mixture of methanol and chloroform (F6). All the fractions were evaluated for their antimicrobial activity, and the F6 fraction was characterized using untargeted metabolomics using SPME-GC×GC-TOFMS. The extracts of A. arvensis F3, F4, and F5 showed antibacterial activity against Staphylococcus aureus ATCC 25923 (5 mg/mL), MRSA BA22038 (5 mg/mL), and Pseudomonas aeruginosa ATCC 27853 (10 mg/mL), and fraction F6 showed antibacterial activity against Staphylococcus aureus ATCC 29213 (2 mg/mL), Escherichia coli ATCC 25922 (20 mg/mL), Pseudomonas aeruginosa ATCC 27853 (10 mg/mL), Enterococcus faecalis ATCC 29212 (10 mg/mL), Staphylococcus aureus 024 (2 mg/mL), and Staphylococcus aureus 003 (2 mg/mL). Metabolomic analysis of F6 revealed 2861 peaks with 58 identified compounds through SPME and 3654 peaks with 29 identified compounds through derivatization. The compounds included methyl ester fatty acids, ethyl ester fatty acids, terpenes, ketones, sugars, amino acids, and fatty acids. This study represents the first exploration of A. arvensis metabolomics and its antimicrobial potential, providing valuable insights for plant classification, phytochemical research, and drug discovery.</description><subject>Amino acids</subject><subject>Analysis</subject><subject>Drug discovery</subject><subject>Drug resistance in microorganisms</subject><subject>Escherichia coli</subject><subject>Fatty acids</subject><subject>Methanol</subject><subject>Methicillin</subject><subject>Terpenes</subject><issn>1420-3049</issn><issn>1420-3049</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNptUL1OwzAYtBBIlMIDsFliTmvHduyMUcVPpCI6lIWlcuzPwciNq9hU6tsTCYYO6Ia74e6kO4TuKVkwVpPlPgYw3wFSqUomlSov0IzykhSM8PryTF-jm5S-CCkpp2KGPpoh-06bDKPXATcm-6PPJ6wHi9-HrMceMlj8Cll3McS9Nwlvxuh88EOPo8NtY3Q4HT411uMRhuTTssWbCIfDLbpyOiS4--M52j49blcvxfrtuV0166KvpCqkYFJKppytVE2VqBSXXVdzzsDVRHBrhOSWWsUrSbUj1BrniKKuszVIK9gcPfzW9jrAzg8u5lGbvU9m10gpptLpj8m1-Mc1wcK0KQ4wLYLzwA8dFmWy</recordid><startdate>20231101</startdate><enddate>20231101</enddate><creator>Thesnor, Valendy</creator><creator>Molinié, Roland</creator><creator>Giebelhaus, Ryland T</creator><creator>de la Mata Espinosa, A. Paulina</creator><creator>Harynuk, James J</creator><creator>Bénimélis, David</creator><creator>Vanhoye, Bérénice</creator><creator>Dunyach-Rémy, Catherine</creator><creator>Sylvestre, Muriel</creator><creator>Cheremond, Yvens</creator><creator>Meffre, Patrick</creator><creator>Cebrián-Torrejón, Gerardo</creator><creator>Benfodda, Zohra</creator><general>MDPI AG</general><scope/></search><sort><creationdate>20231101</creationdate><title>Antibacterial Activity and Untargeted Metabolomics Profiling of IAcalypha arvensis/I Poepp</title><author>Thesnor, Valendy ; Molinié, Roland ; Giebelhaus, Ryland T ; de la Mata Espinosa, A. Paulina ; Harynuk, James J ; Bénimélis, David ; Vanhoye, Bérénice ; Dunyach-Rémy, Catherine ; Sylvestre, Muriel ; Cheremond, Yvens ; Meffre, Patrick ; Cebrián-Torrejón, Gerardo ; Benfodda, Zohra</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g678-75377738fd6891856847bb9443ef9054dc574d1d84671af01dcff081fbd9e7d53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Amino acids</topic><topic>Analysis</topic><topic>Drug discovery</topic><topic>Drug resistance in microorganisms</topic><topic>Escherichia coli</topic><topic>Fatty acids</topic><topic>Methanol</topic><topic>Methicillin</topic><topic>Terpenes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Thesnor, Valendy</creatorcontrib><creatorcontrib>Molinié, Roland</creatorcontrib><creatorcontrib>Giebelhaus, Ryland T</creatorcontrib><creatorcontrib>de la Mata Espinosa, A. Paulina</creatorcontrib><creatorcontrib>Harynuk, James J</creatorcontrib><creatorcontrib>Bénimélis, David</creatorcontrib><creatorcontrib>Vanhoye, Bérénice</creatorcontrib><creatorcontrib>Dunyach-Rémy, Catherine</creatorcontrib><creatorcontrib>Sylvestre, Muriel</creatorcontrib><creatorcontrib>Cheremond, Yvens</creatorcontrib><creatorcontrib>Meffre, Patrick</creatorcontrib><creatorcontrib>Cebrián-Torrejón, Gerardo</creatorcontrib><creatorcontrib>Benfodda, Zohra</creatorcontrib><jtitle>Molecules (Basel, Switzerland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Thesnor, Valendy</au><au>Molinié, Roland</au><au>Giebelhaus, Ryland T</au><au>de la Mata Espinosa, A. Paulina</au><au>Harynuk, James J</au><au>Bénimélis, David</au><au>Vanhoye, Bérénice</au><au>Dunyach-Rémy, Catherine</au><au>Sylvestre, Muriel</au><au>Cheremond, Yvens</au><au>Meffre, Patrick</au><au>Cebrián-Torrejón, Gerardo</au><au>Benfodda, Zohra</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antibacterial Activity and Untargeted Metabolomics Profiling of IAcalypha arvensis/I Poepp</atitle><jtitle>Molecules (Basel, Switzerland)</jtitle><date>2023-11-01</date><risdate>2023</risdate><volume>28</volume><issue>23</issue><issn>1420-3049</issn><eissn>1420-3049</eissn><abstract>The search for potent antimicrobial compounds is critical in the face of growing antibiotic resistance. This study explores Acalypha arvensis Poepp. (A. arvensis), a Caribbean plant traditionally used for disease treatment. The dried plant powder was subjected to successive extractions using different solvents: hexane (F1), dichloromethane (F2), methanol (F3), a 50:50 mixture of methanol and water (F4), and water (F5). Additionally, a parallel extraction was conducted using a 50:50 mixture of methanol and chloroform (F6). All the fractions were evaluated for their antimicrobial activity, and the F6 fraction was characterized using untargeted metabolomics using SPME-GC×GC-TOFMS. The extracts of A. arvensis F3, F4, and F5 showed antibacterial activity against Staphylococcus aureus ATCC 25923 (5 mg/mL), MRSA BA22038 (5 mg/mL), and Pseudomonas aeruginosa ATCC 27853 (10 mg/mL), and fraction F6 showed antibacterial activity against Staphylococcus aureus ATCC 29213 (2 mg/mL), Escherichia coli ATCC 25922 (20 mg/mL), Pseudomonas aeruginosa ATCC 27853 (10 mg/mL), Enterococcus faecalis ATCC 29212 (10 mg/mL), Staphylococcus aureus 024 (2 mg/mL), and Staphylococcus aureus 003 (2 mg/mL). Metabolomic analysis of F6 revealed 2861 peaks with 58 identified compounds through SPME and 3654 peaks with 29 identified compounds through derivatization. The compounds included methyl ester fatty acids, ethyl ester fatty acids, terpenes, ketones, sugars, amino acids, and fatty acids. This study represents the first exploration of A. arvensis metabolomics and its antimicrobial potential, providing valuable insights for plant classification, phytochemical research, and drug discovery.</abstract><pub>MDPI AG</pub><doi>10.3390/molecules28237882</doi></addata></record> |
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subjects | Amino acids Analysis Drug discovery Drug resistance in microorganisms Escherichia coli Fatty acids Methanol Methicillin Terpenes |
title | Antibacterial Activity and Untargeted Metabolomics Profiling of IAcalypha arvensis/I Poepp |
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