Exposure of Tritrichomonas foetus to sublethal doses of metronidazole induces a specific proinflammatory response in murine macrophages.

Tritrichomonas foetus cytokines macrophages metronidazole pro-inflammatory

Journal

The Journal of eukaryotic microbiology
ISSN: 1550-7408
Titre abrégé: J Eukaryot Microbiol
Pays: United States
ID NLM: 9306405

Informations de publication

Date de publication:
04 Sep 2023
Historique:
revised: 22 08 2023
received: 28 06 2023
accepted: 23 08 2023
medline: 5 9 2023
pubmed: 5 9 2023
entrez: 5 9 2023
Statut: aheadofprint

Résumé

Tritrichomonas foetus is a flagellated parasite that primarily infects the reproductive tissues of livestock, causing bovine trichomoniasis. The cytoplasmic membrane of T. foetus contains various compounds that contribute to adherence, colonization, and pathogenicity. Metronidazole (MTZ) is the main treatment for trichomoniasis, but the emergence of drug-resistant strains is a concern due to improper use and dosing. T. foetus infection induces inflammation, and macrophages are key players in the immune response. However, our understanding of the host's immune response to T. foetus is limited, and the specific mechanisms underlying these responses are not well understood. This study aimed to investigate the impact of T. foetus surface proteins from trophozoites cultured under different sublethal MTZ conditions (MTZ-treated T. foetus MPs) on macrophage activation. By analyzing cytokine levels and gene expression in murine macrophages, we demonstrated that MTZ-treated T. foetus MPs induce a specific proinflammatory response. MTZ-treated T. foetus MPs-exposed macrophages exhibited a higher NO and H

Identifiants

pubmed: 37667470
doi: 10.1111/jeu.13000
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13000

Informations de copyright

© 2023 International Society of Protistologists.

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Auteurs

Emanuel Ceballos-Góngora (E)

Laboratorio de Bioquímica y Genética Molecular, Facultad de Química, Universidad Autónoma de Yucatán, Merida, Mexico.
Laboratorio de Farmacología, Facultad de Química, Universidad Autónoma de Yucatán, Merida, Mexico.

Julio César Torres-Romero (JC)

Laboratorio de Bioquímica y Genética Molecular, Facultad de Química, Universidad Autónoma de Yucatán, Merida, Mexico.

Victor Ermilo Arana-Argáez (VE)

Laboratorio de Farmacología, Facultad de Química, Universidad Autónoma de Yucatán, Merida, Mexico.

María Elizbeth Alvarez-Sánchez (ME)

Posgrado en Ciencias Genómicas, Universidad Autónoma de la Ciudad de México, México City, Mexico.

Karla Acosta-Viana (K)

Laboratorio de Biología Celular, Centro de Investigaciones Regionales "Dr. Hideyo Noguchi", Universidad Autónoma de Yucatán, Merida, Mexico.

Antonio Euan-Canto (A)

Laboratorio de Bioquímica y Genética Molecular, Facultad de Química, Universidad Autónoma de Yucatán, Merida, Mexico.
Laboratorio de Farmacología, Facultad de Química, Universidad Autónoma de Yucatán, Merida, Mexico.

Leidi Cristal Alvarez-Sánchez (LC)

Laboratorio de Bioquímica y Genética Molecular, Facultad de Química, Universidad Autónoma de Yucatán, Merida, Mexico.

Classifications MeSH