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Viral Replication and Lung Lesions in BALB/c Mice Experimentally Inoculated with Avian Metapneumovirus Subgroup C Isolated from Chickens

机译:实验从鸡分离出的禽亚肺炎病毒亚组C接种BALB / c小鼠的病毒复制和肺部病变

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摘要

Avian metapneumovirus (aMPV) emerged as an important respiratory pathogen causing acute respiratory tract infection in avian species. Here we used a chicken aMPV subgroup C (aMPV/C) isolate to inoculate experimentally BALB/c mice and found that the aMPV/C can efficiently replicate and persist in the lungs of mice for at least 21 days with a peak viral load at day 6 postinoculation. Lung pathological changes were characterized by increased inflammatory cells. Immunochemical assay showed the presence of viral antigens in the lungs and significant upregulation of pulmonary inflammatory cytokines and chemokines including MCP-1, MIP-1α, RANTES, IL-1β, IFN-γ, and TNF-α were detected following inoculation. These results indicate for the first time that chicken aMPV/C may replicate in the lung of mice. Whether aMPV/C has potential as zoonotic pathogen, further investigation will be required.
机译:禽偏肺病毒(aMPV)作为重要的呼吸道病原体出现,引起禽类急性呼吸道感染。在这里,我们使用鸡aMPV C亚型(aMPV / C)分离株对BALB / c小鼠进行了实验接种,发现aMPV / C可以有效复制并在小鼠的肺中持续至少21天,并且每天病毒载量达到峰值6接种后。肺部病理变化的特征是炎症细胞增多。免疫化学分析显示,接种后肺中存在病毒抗原,并且检测到肺炎性细胞因子和趋化因子(包括MCP-1,MIP-1α,RANTES,IL-1β,IFN-γ和TNF-α)的显着上调。这些结果首次表明,鸡aMPV / C可能在小鼠肺中复制。 aMPV / C是否具有作为人畜共患病原体的潜能,将需要进一步调查。

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