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Phenolic‐rich extracts from acerola, cashew apple and mango by‐products cause diverse inhibitory effects and cell damages on enterotoxigenic Escherichia coli

This study aimed to evaluate the inhibitory effects of phenolic‐rich extracts from acerola (Malpighia emarginata D.C., PEA), cashew apple (Anacardium occidentale L., PEC) and mango (Mangifera indica L., PEM) by‐products on distinct enterotoxigenic Escherichia coli (ETEC) strains. The capability of P...

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Autores principales: da Costa Lima, M., Magnani, M., dos Santos Lima, M., de Sousa, C.P., Dubreuil, J.D., de Souza, E.L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9539876/
https://www.ncbi.nlm.nih.gov/pubmed/34687563
http://dx.doi.org/10.1111/lam.13586
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author da Costa Lima, M.
Magnani, M.
dos Santos Lima, M.
de Sousa, C.P.
Dubreuil, J.D.
de Souza, E.L.
author_facet da Costa Lima, M.
Magnani, M.
dos Santos Lima, M.
de Sousa, C.P.
Dubreuil, J.D.
de Souza, E.L.
author_sort da Costa Lima, M.
collection PubMed
description This study aimed to evaluate the inhibitory effects of phenolic‐rich extracts from acerola (Malpighia emarginata D.C., PEA), cashew apple (Anacardium occidentale L., PEC) and mango (Mangifera indica L., PEM) by‐products on distinct enterotoxigenic Escherichia coli (ETEC) strains. The capability of PEA and PEC of impairing various physiological functions of ETEC strains was investigated with multiparametric flow cytometry. Procyanidin B(2), myricetin and p‐coumaric acid were the major phenolic compounds in PEA, PEC and PEM, respectively. PEA and PEC had lower minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) (MIC: 31·25 mg ml(−1); MBC: 62·5 mg ml(−1)) on ETEC strains than PEM (MIC and MIC: >1000 mg ml(−1)). PEA and PEC (15·6, 31·2, 62·5 mg ml(−1)) caused viable count reductions (P < 0·05) on ETEC strains after 24 h of exposure, notably the ≥3 log reductions caused by 62·5 mg ml(−1). The 24 h exposure of ETEC strains to PEA and PEC (31·2, 62·5 mg ml(−1)) led to high sizes of cell subpopulations with concomitant impairments in cell membrane polarization and permeability, as well as in enzymatic, respiratory and efflux activities. PEA and PEC are effective in inhibiting ETEC through a multi‐target action mode with disturbance in different physiological functions.
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spelling pubmed-95398762022-10-14 Phenolic‐rich extracts from acerola, cashew apple and mango by‐products cause diverse inhibitory effects and cell damages on enterotoxigenic Escherichia coli da Costa Lima, M. Magnani, M. dos Santos Lima, M. de Sousa, C.P. Dubreuil, J.D. de Souza, E.L. Lett Appl Microbiol Original Articles This study aimed to evaluate the inhibitory effects of phenolic‐rich extracts from acerola (Malpighia emarginata D.C., PEA), cashew apple (Anacardium occidentale L., PEC) and mango (Mangifera indica L., PEM) by‐products on distinct enterotoxigenic Escherichia coli (ETEC) strains. The capability of PEA and PEC of impairing various physiological functions of ETEC strains was investigated with multiparametric flow cytometry. Procyanidin B(2), myricetin and p‐coumaric acid were the major phenolic compounds in PEA, PEC and PEM, respectively. PEA and PEC had lower minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) (MIC: 31·25 mg ml(−1); MBC: 62·5 mg ml(−1)) on ETEC strains than PEM (MIC and MIC: >1000 mg ml(−1)). PEA and PEC (15·6, 31·2, 62·5 mg ml(−1)) caused viable count reductions (P < 0·05) on ETEC strains after 24 h of exposure, notably the ≥3 log reductions caused by 62·5 mg ml(−1). The 24 h exposure of ETEC strains to PEA and PEC (31·2, 62·5 mg ml(−1)) led to high sizes of cell subpopulations with concomitant impairments in cell membrane polarization and permeability, as well as in enzymatic, respiratory and efflux activities. PEA and PEC are effective in inhibiting ETEC through a multi‐target action mode with disturbance in different physiological functions. John Wiley and Sons Inc. 2021-11-01 2022-09 /pmc/articles/PMC9539876/ /pubmed/34687563 http://dx.doi.org/10.1111/lam.13586 Text en © 2021 The Authors. Letters in Applied Microbiology published by John Wiley & Sons Ltd on behalf of Society for Applied Microbiology https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
da Costa Lima, M.
Magnani, M.
dos Santos Lima, M.
de Sousa, C.P.
Dubreuil, J.D.
de Souza, E.L.
Phenolic‐rich extracts from acerola, cashew apple and mango by‐products cause diverse inhibitory effects and cell damages on enterotoxigenic Escherichia coli
title Phenolic‐rich extracts from acerola, cashew apple and mango by‐products cause diverse inhibitory effects and cell damages on enterotoxigenic Escherichia coli
title_full Phenolic‐rich extracts from acerola, cashew apple and mango by‐products cause diverse inhibitory effects and cell damages on enterotoxigenic Escherichia coli
title_fullStr Phenolic‐rich extracts from acerola, cashew apple and mango by‐products cause diverse inhibitory effects and cell damages on enterotoxigenic Escherichia coli
title_full_unstemmed Phenolic‐rich extracts from acerola, cashew apple and mango by‐products cause diverse inhibitory effects and cell damages on enterotoxigenic Escherichia coli
title_short Phenolic‐rich extracts from acerola, cashew apple and mango by‐products cause diverse inhibitory effects and cell damages on enterotoxigenic Escherichia coli
title_sort phenolic‐rich extracts from acerola, cashew apple and mango by‐products cause diverse inhibitory effects and cell damages on enterotoxigenic escherichia coli
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9539876/
https://www.ncbi.nlm.nih.gov/pubmed/34687563
http://dx.doi.org/10.1111/lam.13586
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