Activity of propolis from Mexico on the proliferation and virulence factors of Candida albicans.


Journal

BMC microbiology
ISSN: 1471-2180
Titre abrégé: BMC Microbiol
Pays: England
ID NLM: 100966981

Informations de publication

Date de publication:
04 11 2023
Historique:
received: 13 04 2023
accepted: 14 10 2023
medline: 6 11 2023
pubmed: 4 11 2023
entrez: 4 11 2023
Statut: epublish

Résumé

This research evaluated the anti-Candida albicans effect of Mexican propolis from Chihuahua. Chemical composition of the ethanolic extract of propolis was determined by GC-MS, HPLC-DAD, and HPLC-MS. The presence of anthraquinone, aromatic acid, fatty acids, flavonoids, and carbohydrates was revealed. The anti-Candida activity of propolis was determined. The inhibitions halos were between 10.0 to 11.8 mm; 25% minimum inhibitory concentration (0.5 mg/ml) was fungistatic, and 50% minimum inhibitory concentration (1.0 mg/ml) was fungicidal. The effect of propolis on the capability of C. albicans to change its morphology was evaluated. 25% minimum inhibitory concentration inhibited to 50% of germ tube formation. Staining with calcofluor-white and propidium iodide was performed, showing that the propolis affected the integrity of the cell membrane. INT1 gene expression was evaluated by qRT-PCR. Propolis significantly inhibited the expression of the INT1 gene encodes an adhesin (Int1p). Chihuahua propolis extract inhibited the proliferation of Candida albicans, the development of the germ tube, and the synthesis of adhesin INT1. Given the properties demonstrated for Chihuahua propolis, we propose that it is a candidate to be considered as an ideal antifungal agent to help treat this infection since it would not have the toxic effects of conventional antifungals.

Sections du résumé

BACKGROUND
This research evaluated the anti-Candida albicans effect of Mexican propolis from Chihuahua. Chemical composition of the ethanolic extract of propolis was determined by GC-MS, HPLC-DAD, and HPLC-MS. The presence of anthraquinone, aromatic acid, fatty acids, flavonoids, and carbohydrates was revealed.
RESULTS
The anti-Candida activity of propolis was determined. The inhibitions halos were between 10.0 to 11.8 mm; 25% minimum inhibitory concentration (0.5 mg/ml) was fungistatic, and 50% minimum inhibitory concentration (1.0 mg/ml) was fungicidal. The effect of propolis on the capability of C. albicans to change its morphology was evaluated. 25% minimum inhibitory concentration inhibited to 50% of germ tube formation. Staining with calcofluor-white and propidium iodide was performed, showing that the propolis affected the integrity of the cell membrane. INT1 gene expression was evaluated by qRT-PCR. Propolis significantly inhibited the expression of the INT1 gene encodes an adhesin (Int1p). Chihuahua propolis extract inhibited the proliferation of Candida albicans, the development of the germ tube, and the synthesis of adhesin INT1.
CONCLUSIONS
Given the properties demonstrated for Chihuahua propolis, we propose that it is a candidate to be considered as an ideal antifungal agent to help treat this infection since it would not have the toxic effects of conventional antifungals.

Identifiants

pubmed: 37924042
doi: 10.1186/s12866-023-03064-9
pii: 10.1186/s12866-023-03064-9
pmc: PMC10625287
doi:

Substances chimiques

Propolis 9009-62-5
Virulence Factors 0
Antifungal Agents 0
Plant Extracts 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

325

Informations de copyright

© 2023. The Author(s).

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Auteurs

Mario Rodriguez-Canales (M)

Pharmacognosy Laboratory, Biotechnology and Prototypes Unit, Faculty of Higher Studies Iztacala, National Autonomous University of Mexico, Av. de los Barrios No. 1, Los Reyes Iztacala, Tlalnepantla, Edo. de México, C.P. 54090, Mexico. mario.rodcan09@gmail.com.

Yoli Mariana Medina-Romero (YM)

Pharmacognosy Laboratory, Biotechnology and Prototypes Unit, Faculty of Higher Studies Iztacala, National Autonomous University of Mexico, Av. de los Barrios No. 1, Los Reyes Iztacala, Tlalnepantla, Edo. de México, C.P. 54090, Mexico.

Marco Aurelio Rodriguez-Monroy (MA)

Biomedical Research Laboratory in Natural Products, Medicine Career, Faculty of Higher Studies Iztacala, National Autonomous University of Mexico, Avenida de los Barrios Numero 1, Colonia Los Reyes Iztacala, Tlalnepantla, Edo. de Mexico, C.P. 54090, Mexico.

Uriel Nava-Solis (U)

Pharmacognosy Laboratory, Biotechnology and Prototypes Unit, Faculty of Higher Studies Iztacala, National Autonomous University of Mexico, Av. de los Barrios No. 1, Los Reyes Iztacala, Tlalnepantla, Edo. de México, C.P. 54090, Mexico.

Sandra Isabel Bolaños-Cruz (SI)

Pharmacognosy Laboratory, Biotechnology and Prototypes Unit, Faculty of Higher Studies Iztacala, National Autonomous University of Mexico, Av. de los Barrios No. 1, Los Reyes Iztacala, Tlalnepantla, Edo. de México, C.P. 54090, Mexico.

Maria Jimena Mendoza-Romero (MJ)

Pharmacognosy Laboratory, Biotechnology and Prototypes Unit, Faculty of Higher Studies Iztacala, National Autonomous University of Mexico, Av. de los Barrios No. 1, Los Reyes Iztacala, Tlalnepantla, Edo. de México, C.P. 54090, Mexico.

Jorge E Campos (JE)

Molecular Biochemistry Laboratory, Biotechnology and Prototypes Unit, Faculty of Higher Studies Iztacala, National Autonomous University of Mexico, Av. de los Barrios No. 1, Los Reyes Iztacala, Tlalnepantla, Edo. de México, C.P. 54090, México.

Ana Bertha Hernandez-Hernandez (AB)

Pharmacognosy Laboratory, Biotechnology and Prototypes Unit, Faculty of Higher Studies Iztacala, National Autonomous University of Mexico, Av. de los Barrios No. 1, Los Reyes Iztacala, Tlalnepantla, Edo. de México, C.P. 54090, Mexico.

Yolanda I Chirino (YI)

Laboratory 10, Carcinogenesis and Toxicology, Biomedicine Unit, Faculty of Higher Studies Iztacala, National Autonomous University of Mexico, Avenida de los Barrios Numero 1, Colonia Los Reyes Iztacala, Tlalnepantla, Edo. de Mexico, C.P. 54090, Mexico.

Tonatiuh Cruz-Sanchez (T)

Propolis Analysis Service Laboratory, Faculty of Higher Studies Cuautitlan, National Autonomous University of Mexico, Av. Teoloyucan Km 2.5, San Sebastian Xhala, Cuautitlán Izcalli, Edo. de México, C.P. 54714, México.

Carlos Gerardo Garcia-Tovar (CG)

Laboratory of Veterinary Morphology and Cell Biology, Faculty of Higher Studies Cuautitlan, National Autonomous University of Mexico, Av. Teoloyucan Km 2.5, San Sebastian Xhala, Cuautitlán Izcalli, Estado de México, CP 54714, México.

Maria Margarita Canales-Martinez (MM)

Pharmacognosy Laboratory, Biotechnology and Prototypes Unit, Faculty of Higher Studies Iztacala, National Autonomous University of Mexico, Av. de los Barrios No. 1, Los Reyes Iztacala, Tlalnepantla, Edo. de México, C.P. 54090, Mexico. dra.margaritacanales@gmail.com.

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Classifications MeSH