Cytokine and goblet cell gene expression in equine cyathostomin infection and larvicidal anthelmintic therapy

Ashley E. Steuer, John C. Stewart, Virginia D. Barker, Amanda A. Adams, Martin K. Nielsen

Producción científica: Articlerevisión exhaustiva

6 Citas (Scopus)

Resumen

Aims: The role of the immune response to cyathostomin infections in horses remains unknown. Intestinal goblet cell hyperplasia has previously been noted as a component in cyathostomin infection; however, the function is unclear. The goal of this study was to evaluate the local and systemic gene expression to cyathostomin infections following larvicidal treatment and explore their relation to goblet cells. Methods and Results: Thirty-six ponies with naturally acquired cyathostomin infections were randomly allocated into three groups: fenbendazole-treated (10 mg/kg PO 5 days), moxidectin-treated (0.4 mg/kg PO once) and untreated control. Whole blood from all horses was collected weekly, and tissue samples from the large intestine collected during necropsy at 2 and 5 weeks post-treatment (WPT). Gene expression of interleukin (IL)-4, IL-5, IL-6, IL-10, IL-13, IL-17A, IL-22, IFN-γ, resistin-like molecule beta (RELM-β), Mucin 2 (MUC2) and tumour necrosis factor (TNF)-α was measured using qRT-PCR. There were statistically significant linear correlations between luminal worm burdens and MUC2 (r = −.2358) and RELM-β (r = −.2261). Conclusion: This suggests an active role of immune system post-treatment in parasite expulsion, specifically in goblet cells, and that the organs respond differently to treatment and the larvae themselves. This may have implications in the disease process and treatment.

Idioma originalEnglish
Número de artículoe12709
PublicaciónParasite Immunology
Volumen42
N.º6
DOI
EstadoPublished - jun 1 2020

Nota bibliográfica

Publisher Copyright:
© 2020 John Wiley & Sons Ltd

Financiación

Funding was provided by Zoetis, LLC, Kalamazoo, MI, United States, grant number 18ERGPAR‐01‐01.

FinanciadoresNúmero del financiador
Zoetis18ERGPAR‐01‐01

    ASJC Scopus subject areas

    • Parasitology
    • Immunology

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