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Bioassay-Guided Isolation of Antimicrobial Components and LC/QToF Profile of Plumeria obtusa: Potential for the Treatment of Antimicrobial Resistance

[Image: see text] The methanolic fraction (M-F) of the total extract (TE) of Plumeria obtusa L. aerial parts showed promising antibacterial effects against the MDR (multidrug-resistant) gram-negative pathogens Klebsiella pneumoniae and Escherichia coli O157:H7 [Shiga toxin-producing E. coli (STEC)]....

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Autores principales: Eloutify, Yousra Tarek, El-Shiekh, Riham A., Ibrahim, Khaled Meselhy, Elshimy, Rana, Avula, Bharathi, Katragunta, Kumar, Khan, Ikhlas A., Meselhy, Meselhy R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9947952/
https://www.ncbi.nlm.nih.gov/pubmed/36844537
http://dx.doi.org/10.1021/acsomega.2c06803
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author Eloutify, Yousra Tarek
El-Shiekh, Riham A.
Ibrahim, Khaled Meselhy
Elshimy, Rana
Avula, Bharathi
Katragunta, Kumar
Khan, Ikhlas A.
Meselhy, Meselhy R.
author_facet Eloutify, Yousra Tarek
El-Shiekh, Riham A.
Ibrahim, Khaled Meselhy
Elshimy, Rana
Avula, Bharathi
Katragunta, Kumar
Khan, Ikhlas A.
Meselhy, Meselhy R.
author_sort Eloutify, Yousra Tarek
collection PubMed
description [Image: see text] The methanolic fraction (M-F) of the total extract (TE) of Plumeria obtusa L. aerial parts showed promising antibacterial effects against the MDR (multidrug-resistant) gram-negative pathogens Klebsiella pneumoniae and Escherichia coli O157:H7 [Shiga toxin-producing E. coli (STEC)]. In addition, M-F had a synergistic effect (in combination with vancomycin) against the MDR gram-positive strains MRSA (methicillin-resistant Staphylococcus aureus) and Bacillus cereus. After treating the K. pneumoniae- and STEC-infected mice with M-F (25 mg/kg, i.p.), the level of IgM and TNF-α was decreased and the severity of pathological lesions were reduced better than that observed after administration of gentamycin (33 mg/kg, i.p.). Thirty-seven compounds including 10 plumeria-type iridoids and 18 phenolics, 7 quinoline derivatives, 1 amino acid, and 1 fatty acid were identified in TE using LC/ESI-QToF. Furthermore, five compounds; kaempferol 3-O-rutinoside (M1), quercetin 3-O-rutinoside (M2), glochiflavanoside B (M3), plumieride (M4), and 13-O-caffeoylplumieride (M5) were isolated from M-F. M5 was active against K. pneumoniae (MIC of 64 μg/mL) and STEC (MIC of 32 μg/mL). These findings suggested that M-F and M5 are promising antimicrobial natural products for combating MDR K. pneumoniae and STEC nosocomial infections.
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spelling pubmed-99479522023-02-24 Bioassay-Guided Isolation of Antimicrobial Components and LC/QToF Profile of Plumeria obtusa: Potential for the Treatment of Antimicrobial Resistance Eloutify, Yousra Tarek El-Shiekh, Riham A. Ibrahim, Khaled Meselhy Elshimy, Rana Avula, Bharathi Katragunta, Kumar Khan, Ikhlas A. Meselhy, Meselhy R. ACS Omega [Image: see text] The methanolic fraction (M-F) of the total extract (TE) of Plumeria obtusa L. aerial parts showed promising antibacterial effects against the MDR (multidrug-resistant) gram-negative pathogens Klebsiella pneumoniae and Escherichia coli O157:H7 [Shiga toxin-producing E. coli (STEC)]. In addition, M-F had a synergistic effect (in combination with vancomycin) against the MDR gram-positive strains MRSA (methicillin-resistant Staphylococcus aureus) and Bacillus cereus. After treating the K. pneumoniae- and STEC-infected mice with M-F (25 mg/kg, i.p.), the level of IgM and TNF-α was decreased and the severity of pathological lesions were reduced better than that observed after administration of gentamycin (33 mg/kg, i.p.). Thirty-seven compounds including 10 plumeria-type iridoids and 18 phenolics, 7 quinoline derivatives, 1 amino acid, and 1 fatty acid were identified in TE using LC/ESI-QToF. Furthermore, five compounds; kaempferol 3-O-rutinoside (M1), quercetin 3-O-rutinoside (M2), glochiflavanoside B (M3), plumieride (M4), and 13-O-caffeoylplumieride (M5) were isolated from M-F. M5 was active against K. pneumoniae (MIC of 64 μg/mL) and STEC (MIC of 32 μg/mL). These findings suggested that M-F and M5 are promising antimicrobial natural products for combating MDR K. pneumoniae and STEC nosocomial infections. American Chemical Society 2023-02-08 /pmc/articles/PMC9947952/ /pubmed/36844537 http://dx.doi.org/10.1021/acsomega.2c06803 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Eloutify, Yousra Tarek
El-Shiekh, Riham A.
Ibrahim, Khaled Meselhy
Elshimy, Rana
Avula, Bharathi
Katragunta, Kumar
Khan, Ikhlas A.
Meselhy, Meselhy R.
Bioassay-Guided Isolation of Antimicrobial Components and LC/QToF Profile of Plumeria obtusa: Potential for the Treatment of Antimicrobial Resistance
title Bioassay-Guided Isolation of Antimicrobial Components and LC/QToF Profile of Plumeria obtusa: Potential for the Treatment of Antimicrobial Resistance
title_full Bioassay-Guided Isolation of Antimicrobial Components and LC/QToF Profile of Plumeria obtusa: Potential for the Treatment of Antimicrobial Resistance
title_fullStr Bioassay-Guided Isolation of Antimicrobial Components and LC/QToF Profile of Plumeria obtusa: Potential for the Treatment of Antimicrobial Resistance
title_full_unstemmed Bioassay-Guided Isolation of Antimicrobial Components and LC/QToF Profile of Plumeria obtusa: Potential for the Treatment of Antimicrobial Resistance
title_short Bioassay-Guided Isolation of Antimicrobial Components and LC/QToF Profile of Plumeria obtusa: Potential for the Treatment of Antimicrobial Resistance
title_sort bioassay-guided isolation of antimicrobial components and lc/qtof profile of plumeria obtusa: potential for the treatment of antimicrobial resistance
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9947952/
https://www.ncbi.nlm.nih.gov/pubmed/36844537
http://dx.doi.org/10.1021/acsomega.2c06803
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