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Anti-Proteus Activity, Anti-Struvite Crystal, and Phytochemical Analysis of Sida acuta Burm. F. Ethanolic Leaf Extract

Proteus mirabilis is a significant cause of urinary tract infection that may contribute to struvite stones. Anti-infection of this bacterium and anti-struvite formation must be considered. Sida acuta Burm. F. (SA) has been used for the treatment of diseases related to kidneys. Therefore, we investig...

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Autores principales: Smanthong, Nitis, Tavichakorntrakool, Ratree, Tippayawat, Patcharaporn, Lulitanond, Aroonlug, Pinlaor, Porntip, Daduang, Jureerut, Sae-ung, Nattaya, Chaveerach, Arunrat, Phetcharaburanin, Jutarop, Boonsiri, Patcharee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8838957/
https://www.ncbi.nlm.nih.gov/pubmed/35164357
http://dx.doi.org/10.3390/molecules27031092
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author Smanthong, Nitis
Tavichakorntrakool, Ratree
Tippayawat, Patcharaporn
Lulitanond, Aroonlug
Pinlaor, Porntip
Daduang, Jureerut
Sae-ung, Nattaya
Chaveerach, Arunrat
Phetcharaburanin, Jutarop
Boonsiri, Patcharee
author_facet Smanthong, Nitis
Tavichakorntrakool, Ratree
Tippayawat, Patcharaporn
Lulitanond, Aroonlug
Pinlaor, Porntip
Daduang, Jureerut
Sae-ung, Nattaya
Chaveerach, Arunrat
Phetcharaburanin, Jutarop
Boonsiri, Patcharee
author_sort Smanthong, Nitis
collection PubMed
description Proteus mirabilis is a significant cause of urinary tract infection that may contribute to struvite stones. Anti-infection of this bacterium and anti-struvite formation must be considered. Sida acuta Burm. F. (SA) has been used for the treatment of diseases related to kidneys. Therefore, we investigated the effects of the SA leaf ethanolic extract (SAEE) on growth and on virulent factors (swarming motility and urease activity) of Proteus mirabilis isolated from kidney stone formers. We also evaluated anti-struvite crystal formation and phytochemical constituents of SAEE. The minimum inhibitory concentrations (MICs) of SAEE against three clinical P. mirabilis isolates were 8 mg/mL. Intriguingly, the 1/2MIC of SAEE had significant inhibitory effects on the swarming motility and urease activity of clinical P. mirabilis isolates when compared with the condition without SAEE. The SAEE at the various concentrations significantly inhibited the average weights of struvite crystals in a dose-dependent manner, compared with the control. The phytochemical analysis revealed that SAEE contained catechin, chlorogenic acid, rutin, and ferulic acid. This study indicated that SAEE has anti-P. mirabilis and anti-struvite crystal activities via its bioactive compounds. For this reason, SAEE may be developed as a new agent for the treatment of struvite stone induced by P. mirabilis.
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spelling pubmed-88389572022-02-13 Anti-Proteus Activity, Anti-Struvite Crystal, and Phytochemical Analysis of Sida acuta Burm. F. Ethanolic Leaf Extract Smanthong, Nitis Tavichakorntrakool, Ratree Tippayawat, Patcharaporn Lulitanond, Aroonlug Pinlaor, Porntip Daduang, Jureerut Sae-ung, Nattaya Chaveerach, Arunrat Phetcharaburanin, Jutarop Boonsiri, Patcharee Molecules Article Proteus mirabilis is a significant cause of urinary tract infection that may contribute to struvite stones. Anti-infection of this bacterium and anti-struvite formation must be considered. Sida acuta Burm. F. (SA) has been used for the treatment of diseases related to kidneys. Therefore, we investigated the effects of the SA leaf ethanolic extract (SAEE) on growth and on virulent factors (swarming motility and urease activity) of Proteus mirabilis isolated from kidney stone formers. We also evaluated anti-struvite crystal formation and phytochemical constituents of SAEE. The minimum inhibitory concentrations (MICs) of SAEE against three clinical P. mirabilis isolates were 8 mg/mL. Intriguingly, the 1/2MIC of SAEE had significant inhibitory effects on the swarming motility and urease activity of clinical P. mirabilis isolates when compared with the condition without SAEE. The SAEE at the various concentrations significantly inhibited the average weights of struvite crystals in a dose-dependent manner, compared with the control. The phytochemical analysis revealed that SAEE contained catechin, chlorogenic acid, rutin, and ferulic acid. This study indicated that SAEE has anti-P. mirabilis and anti-struvite crystal activities via its bioactive compounds. For this reason, SAEE may be developed as a new agent for the treatment of struvite stone induced by P. mirabilis. MDPI 2022-02-06 /pmc/articles/PMC8838957/ /pubmed/35164357 http://dx.doi.org/10.3390/molecules27031092 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Smanthong, Nitis
Tavichakorntrakool, Ratree
Tippayawat, Patcharaporn
Lulitanond, Aroonlug
Pinlaor, Porntip
Daduang, Jureerut
Sae-ung, Nattaya
Chaveerach, Arunrat
Phetcharaburanin, Jutarop
Boonsiri, Patcharee
Anti-Proteus Activity, Anti-Struvite Crystal, and Phytochemical Analysis of Sida acuta Burm. F. Ethanolic Leaf Extract
title Anti-Proteus Activity, Anti-Struvite Crystal, and Phytochemical Analysis of Sida acuta Burm. F. Ethanolic Leaf Extract
title_full Anti-Proteus Activity, Anti-Struvite Crystal, and Phytochemical Analysis of Sida acuta Burm. F. Ethanolic Leaf Extract
title_fullStr Anti-Proteus Activity, Anti-Struvite Crystal, and Phytochemical Analysis of Sida acuta Burm. F. Ethanolic Leaf Extract
title_full_unstemmed Anti-Proteus Activity, Anti-Struvite Crystal, and Phytochemical Analysis of Sida acuta Burm. F. Ethanolic Leaf Extract
title_short Anti-Proteus Activity, Anti-Struvite Crystal, and Phytochemical Analysis of Sida acuta Burm. F. Ethanolic Leaf Extract
title_sort anti-proteus activity, anti-struvite crystal, and phytochemical analysis of sida acuta burm. f. ethanolic leaf extract
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8838957/
https://www.ncbi.nlm.nih.gov/pubmed/35164357
http://dx.doi.org/10.3390/molecules27031092
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