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H9N2禽流感病毒感染BALB/c小鼠过程中IFITM1和IFITM3的表达谱及组织学分布

Expression profile and histological distribution of IFITM1 and IFITM3 during H9N2 avian influenza virus infection in BALB/c mice.

作者信息

Yu Meng, Qi Wenbao, Huang Zhiqiang, Zhang Kaizhao, Ye Jinhui, Liu Rongchang, Wang Heng, Ma Yongjiang, Liao Ming, Ning Zhangyong

机构信息

College of Veterinary Medicine, South China Agricultural University, Guangzhou, 510642, People's Republic of China.

出版信息

Med Microbiol Immunol. 2015 Aug;204(4):505-14. doi: 10.1007/s00430-014-0361-2. Epub 2014 Sep 30.

Abstract

The H9N2 avian influenza virus is a pandemic threat which has repeatedly caused infection in humans and shows enhanced replication and transmission in mice. Previous reports showed that host factors, the interferon-inducible transmembrane (IFITM) protein, can block the replication of pathogens and affect their pathogenesis. BALB/c mice are routine laboratory animals used in influenza virus research, but the effects of H9N2 influenza virus on tissue distribution and expression pattern of IFITM in these mice are unknown. Here, we investigated the expression patterns and tissue distribution of IFITM1 and IFITM3 in BALB/c mice by infection with H9N2 AIV strains with only a PB2 residue 627 difference. The results showed that the expression patterns of ITITM1 and IFITM3 differ in various tissues of BALB/c mice at different time points after infection. IFITM1 and IFITM3 showed cell- and tissue-specific distribution in the lung, heart, liver, spleen, kidney and brain. Notably, the epithelial and neuronal cells all expressed the proteins of IFITM1 and IFITM3. Our results provide the first look at differences in IFITM1 and IFITM3 expression patterns in BALB/c mice infected by H9N2 influenza viruses. This will enhance research on the interaction between AIV and host and further will elucidate the pathogenesis of influenza virus infection based on the interferon-inducible transmembrane (IFITM) protein.

摘要

H9N2禽流感病毒是一种大流行威胁,它多次导致人类感染,并在小鼠中显示出增强的复制和传播能力。先前的报道表明,宿主因子干扰素诱导跨膜(IFITM)蛋白可以阻断病原体的复制并影响其发病机制。BALB/c小鼠是流感病毒研究中常用的常规实验动物,但H9N2流感病毒对这些小鼠中IFITM的组织分布和表达模式的影响尚不清楚。在此,我们通过感染仅PB2残基627存在差异的H9N2禽流感病毒株,研究了BALB/c小鼠中IFITM1和IFITM3的表达模式和组织分布。结果表明,感染后不同时间点,BALB/c小鼠不同组织中ITITM1和IFITM3的表达模式存在差异。IFITM1和IFITM3在肺、心脏、肝脏、脾脏、肾脏和大脑中表现出细胞和组织特异性分布。值得注意的是,上皮细胞和神经元细胞均表达IFITM1和IFITM3蛋白。我们的结果首次揭示了感染H9N2流感病毒的BALB/c小鼠中IFITM1和IFITM3表达模式的差异。这将加强对禽流感病毒与宿主相互作用的研究,并进一步阐明基于干扰素诱导跨膜(IFITM)蛋白的流感病毒感染发病机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcb2/7087031/3a550c17a4e9/430_2014_361_Fig1_HTML.jpg

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