Administration of a Recombinant Fusion Protein of IFN-γ and CD154 Inhibited the Infection of Chicks with <i>Salmonella enterica</i>
The cytokines IFN-γ and CD154 have been well established, and they play pivotal roles in immune protection against <i>Salmonella</i> in mice, but their effects and specific mechanisms in <i>Salmonella</i>-infected chickens are less understood. In this study, we conducted anim...
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| Main Authors: | , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2025-02-01
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| Series: | Veterinary Sciences |
| Subjects: | |
| Online Access: | https://www.mdpi.com/2306-7381/12/2/112 |
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| Summary: | The cytokines IFN-γ and CD154 have been well established, and they play pivotal roles in immune protection against <i>Salmonella</i> in mice, but their effects and specific mechanisms in <i>Salmonella</i>-infected chickens are less understood. In this study, we conducted animal experiments to screen the highly immunoprotective chIFN-γ-chCD154 fusion protein compared with single protein chIFN-γ or chCD154 in white Leghorn chickens. The results showed that compared with separate pretreatments with chIFN-γ and chCD154, the fusion protein, chIFN-γ-chCD154, synergistically increased survival of infected chickens, reduced bacterial load in feces and organs, and attenuated pathological damage to the liver and cecum. Pretreatment with chIFN-γ-chCD154 also increased humoral immune responses, expression of the tight junction proteins zo-1, occludin, and claudin-1, and the relative abundance of <i>Enterococcus_cecorum</i>, <i>Lactobacillus_helveticus</i>, and <i>Lactobacillus_agilis</i>, which protect against intestinal inflammation. Compared with single protein pretreatment, chIFN-γ-chCD154 significantly upregulated STAT1, IRF1, and GBP1 in infected chickens while decreasing mRNA expression of TLR4, MyD88, NF-κB, TNF-α, IL-6, and IL-1β. In summary, damage to the cecal epithelial barrier and the inflammation induced by <i>S. typhimurium</i> infection was alleviated by chIFN-γ-chCD154 pretreatment through a mechanism involving the TLR4/MyD88/NF-κB and IFN-γ/STAT/IRF1/GBP1 pathways. |
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| ISSN: | 2306-7381 |