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富含间苯三酚鞣质的海藻提取物可抑制流感感染。

Phlorotannin-Rich Seaweed Extract Inhibits Influenza Infection.

作者信息

Mega Daniele F, Sharma Parul, Kipar Anja, Hetzel Udo, Bramwell Chloe, Merritt Alan, Wright Samuel, Plummer Chris, Urbanowicz Richard A, Stewart James P

机构信息

Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool L3 5RF, UK.

Laboratory for Animal Model Pathology, Institute of Veterinary Pathology, University of Zurich, 8057 Zürich, Switzerland.

出版信息

Viruses. 2024 Dec 15;16(12):1919. doi: 10.3390/v16121919.

Abstract

Seaweed-derived compounds are a renewable resource utilised in the manufacturing and food industry. This study focuses on an enriched seaweed extract (ESE) isolated from The ESE was screened for antiviral activity by plaque reduction assays against influenza A/Puerto Rico/8/1934 H1N1 (PR8), A/X-31 H3N2 (X31) and A/England/195/2009 H1N1 (Eng195), resulting in the complete inhibition of infection. Time of addition assays and FACS analysis were used to help determine the modes of action. The therapeutic potential of ESE was then explored using differentiated human bronchiole epithelial cells at the air-liquid interphase and a murine model challenged with IAV. The data indicates that ESE primarily interacts directly with virions, reducing mean virus-cell binding by 79.3% with 0.01 mg/mL ESE. Interestingly, ESE also inhibits the early and late stages of the influenza A lifecycle when treatment occurs after cell binding. This inhibitory effect appears to reduce the internalisation of the virus and the release of progeny virus by targeting neuraminidase activity, with IC50 values of 0.5 μg/mL for X31, 3.2 μg/mL for Eng195 and 12.8 μg/mL for PR8. The intranasal administration of 5 mg/kg ESE in mice infected with IAV reduced the viral load in lung tissue. ESE may be a promising broad-acting antiviral agent in the treatment of influenza infections.

摘要

海藻衍生化合物是一种可再生资源,用于制造业和食品工业。本研究聚焦于从[具体海藻名称未给出]中分离出的一种富集海藻提取物(ESE)。通过针对甲型流感病毒/波多黎各/8/1934 H1N1(PR8)、甲型流感病毒/ X - 31 H3N2(X31)和甲型流感病毒/英格兰/195/2009 H1N1(Eng195)的蚀斑减少试验,对ESE进行抗病毒活性筛选,结果显示其能完全抑制感染。采用加样时间试验和流式细胞术分析来帮助确定其作用方式。然后利用气液界面分化的人细支气管上皮细胞和感染甲型流感病毒的小鼠模型,探索ESE的治疗潜力。数据表明,ESE主要直接与病毒粒子相互作用,0.01 mg/mL的ESE可使平均病毒 - 细胞结合减少79.3%。有趣的是,当在细胞结合后进行处理时,ESE还能抑制甲型流感病毒生命周期的早期和晚期阶段。这种抑制作用似乎通过靶向神经氨酸酶活性来减少病毒的内化和子代病毒的释放,其对X31的IC50值为0.5 μg/mL,对Eng195为3.2 μg/mL,对PR8为12.8 μg/mL。对感染甲型流感病毒的小鼠鼻内给予5 mg/kg的ESE可降低肺组织中的病毒载量。ESE可能是一种有前景的广谱抗病毒剂,可用于治疗流感感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ed2/11680388/d34ddeee4733/viruses-16-01919-g001.jpg

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