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金黄色葡萄球菌脂肪酶 1 增强甲型流感病毒复制。

Staphylococcus aureus Lipase 1 Enhances Influenza A Virus Replication.

机构信息

The Roslin Institute, University of Edinburgh, Midlothian, United Kingdom.

The Roslin Institute, University of Edinburgh, Midlothian, United Kingdom

出版信息

mBio. 2020 Jul 7;11(4):e00975-20. doi: 10.1128/mBio.00975-20.

DOI:10.1128/mBio.00975-20
PMID:32636247
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7343990/
Abstract

Influenza A virus (IAV) causes annual epidemics of respiratory disease in humans, often complicated by secondary coinfection with bacterial pathogens such as Here, we report that the secreted protein lipase 1 enhances IAV replication in primary cells, including human lung fibroblasts. The proviral activity of lipase 1 is dependent on its enzymatic function, acts late in the viral life cycle, and results in increased infectivity through positive modulation of virus budding. Furthermore, the proviral effect of lipase 1 on IAV is exhibited during infection of embryonated hen's eggs and, importantly, increases the yield of a vaccine strain of IAV by approximately 5-fold. Thus, we have identified the first protein to enhance IAV replication, suggesting a potential role in coinfection. Importantly, this activity may be harnessed to address global shortages of influenza vaccines. Influenza A virus (IAV) causes annual epidemics and sporadic pandemics of respiratory disease. Secondary bacterial coinfection by organisms such as is the most common complication of primary IAV infection and is associated with high levels of morbidity and mortality. Here, we report the first identified factor (lipase 1) that enhances IAV replication during infection via positive modulation of virus budding. The effect is observed in embryonated hen's eggs and greatly enhances the yield of a vaccine strain, a finding that could be applied to address global shortages of influenza vaccines.

摘要

甲型流感病毒(IAV)每年都会引起人类呼吸道疾病的流行,常伴有细菌病原体的继发感染,如 。在这里,我们报告说, 分泌的蛋白脂肪酶 1 增强了 IAV 在原代细胞中的复制,包括人肺成纤维细胞。脂肪酶 1 的前病毒活性依赖于其酶功能,在病毒生命周期的晚期发挥作用,并通过正调控病毒出芽增加感染性。此外,脂肪酶 1 对 IAV 的前病毒作用在鸡胚感染中表现出来,重要的是,它使 IAV 疫苗株的产量增加了约 5 倍。因此,我们已经确定了第一个增强 IAV 复制的 蛋白,这表明它在继发感染中可能具有潜在作用。重要的是,这种活性可能被用来解决全球流感疫苗短缺的问题。甲型流感病毒(IAV)每年都会引起呼吸道疾病的流行和偶发性大流行。由 等生物体引起的继发性细菌继发感染是原发性 IAV 感染最常见的并发症,与高发病率和死亡率有关。在这里,我们报告了第一个被识别的 因子(脂肪酶 1),它通过正调控病毒出芽来增强 IAV 感染期间的复制。这一效应在鸡胚中观察到,并大大提高了疫苗株的产量,这一发现可用于解决全球流感疫苗短缺的问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/645d/7343990/2e266f57768b/mBio.00975-20-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/645d/7343990/7830b6cb750d/mBio.00975-20-f0001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/645d/7343990/bc3f9986ac61/mBio.00975-20-f0003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/645d/7343990/dd9389cb7249/mBio.00975-20-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/645d/7343990/2e266f57768b/mBio.00975-20-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/645d/7343990/7830b6cb750d/mBio.00975-20-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/645d/7343990/2f5327c1c73d/mBio.00975-20-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/645d/7343990/bc3f9986ac61/mBio.00975-20-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/645d/7343990/f4a09ddfa8b8/mBio.00975-20-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/645d/7343990/dd9389cb7249/mBio.00975-20-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/645d/7343990/2e266f57768b/mBio.00975-20-f0006.jpg

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