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反刍动物 I 型干扰素诱导的抗病毒状态对同源副流感病毒 3 攻击的体外时间动态。

Temporal Dynamics of the Ruminant Type I IFN-Induced Antiviral State against Homologous Parainfluenza Virus 3 Challenge In Vitro.

机构信息

Institute of Veterinary Medicine, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, China.

School of Life Sciences, Jiangsu University, Zhenjiang 212013, China.

出版信息

Viruses. 2022 May 11;14(5):1025. doi: 10.3390/v14051025.

DOI:10.3390/v14051025
PMID:35632770
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9146716/
Abstract

Viruses have evolved diverse strategies to evade the antiviral response of interferons (IFNs). Exogenous IFNs were applied to eliminate the counteracting effect and possess antiviral properties. Caprine parainfluenza virus 3 (CPIV3) and bovine parainfluenza virus type 3 (BPIV3) are important pathogens associated with respiratory diseases in goat and cattle, respectively. To explore the feasibility of type I IFNs for control of CPIV3 and BPIV3 infection, the activated effects of IFN-stimulated genes (ISGs) and the immunomodulation responses of goat IFN-α were detected by transcriptomic analysis. Then, the antiviral efficacy of goat IFN-α and IFN-τ against CPIV3 and BPIV3 infection in MDBK cells was evaluated using different treatment routes at different infection times. The results showed that CPIV3 infection inhibited the production of type I IFNs, whereas exogenous goat IFN-α induced various ISGs, the IFN-τ encoding gene, and a negligible inflammatory response. Consequently, goat IFN-α prophylaxis but not treatment was found to effectively modulate CPIV3 and BPIV3 infection; the protective effect lasted for 1 week, and the antiviral activity was maintained at a concentration of 0.1 μg/mL. Furthermore, the antiviral activity of goat IFN-τ in response to CPIV3 and BPIV3 infection is comparable to that of goat IFN-α. These results corroborate that goat IFN-α and IFN-τ exhibit prophylactic activities in response to ruminant respiratory viral infection in vitro, and should be further investigated for a potential use in vivo.

摘要

病毒进化出了多种策略来逃避干扰素(IFN)的抗病毒反应。外源性 IFN 被应用于消除拮抗作用并具有抗病毒特性。山羊副流感病毒 3(CPIV3)和牛副流感病毒 3 型(BPIV3)分别是导致山羊和牛呼吸道疾病的重要病原体。为了探索 I 型 IFNs 控制 CPIV3 和 BPIV3 感染的可行性,通过转录组分析检测了 IFN 刺激基因(ISGs)的激活作用和山羊 IFN-α的免疫调节反应。然后,通过在不同感染时间采用不同的处理途径,评估了山羊 IFN-α和 IFN-τ对 MDBK 细胞中 CPIV3 和 BPIV3 感染的抗病毒功效。结果表明,CPIV3 感染抑制了 I 型 IFN 的产生,而外源性山羊 IFN-α诱导了各种 ISGs、IFN-τ 编码基因和轻微的炎症反应。因此,发现山羊 IFN-α预防而非治疗可有效调节 CPIV3 和 BPIV3 感染;保护作用持续 1 周,抗病毒活性在 0.1μg/mL 的浓度下得以维持。此外,山羊 IFN-τ 对 CPIV3 和 BPIV3 感染的抗病毒活性与山羊 IFN-α相当。这些结果证实了山羊 IFN-α和 IFN-τ在体外对反刍动物呼吸道病毒感染具有预防作用,应进一步在体内进行研究以探索其潜在用途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e902/9146716/bfc8311feafc/viruses-14-01025-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e902/9146716/126d9c51fdda/viruses-14-01025-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e902/9146716/f37476762b51/viruses-14-01025-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e902/9146716/9af62b9ed42a/viruses-14-01025-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e902/9146716/a14dec42fc99/viruses-14-01025-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e902/9146716/4613d707bdd6/viruses-14-01025-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e902/9146716/bfc8311feafc/viruses-14-01025-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e902/9146716/126d9c51fdda/viruses-14-01025-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e902/9146716/f37476762b51/viruses-14-01025-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e902/9146716/9af62b9ed42a/viruses-14-01025-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e902/9146716/a14dec42fc99/viruses-14-01025-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e902/9146716/4613d707bdd6/viruses-14-01025-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e902/9146716/bfc8311feafc/viruses-14-01025-g006.jpg

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