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首页> 外文期刊>Veterinary research >Crosstalk between H9N2 avian influenza virus and crypt-derived intestinal organoids
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Crosstalk between H9N2 avian influenza virus and crypt-derived intestinal organoids

机译:H9N2禽流感病毒与隐窝来源的肠道类器官之间的串扰

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The spread of Avian influenza virus via animal feces makes the virus difficult to prevent, which causes great threat to human health. Therefore, it is imperative to understand the survival and invasion mechanism of H9N2 virus in the intestinal mucosa. In this study, we used mouse threedimensional intestinal organoids that contained intestinal crypts and villi differentiated from intestinal stem cells to explore interactions between H9N2 avian influenza virus and the intestinal mucosa. The HA, NA, NP and PB1 genes of H9N2 viruses could be detected in intestinal organoids at 1 h, and reached peak levels at 48 h post-infection. Moreover, the HA and NP proteins of H9N2 virus could also be detected in organoids via immunofluorescence. Virus invasion caused damage to intestinal organoids with reduced mRNA transcript expression of Wnt3, Dll1 and Dll4. The abnormal growth of intestinal organoids may be attributed to the loss of Paneth cells, as indicated by the low mRNA transcript levels of lyz1 and defcr1. This present study demonstrates that H9N2 virus could invade intestinal organoids and then cause damage, as well as affect intestinal stem cell proliferation and differentiation, promoting the loss of Paneth cells.
机译:禽流感病毒通过动物粪便的传播使该病毒难以预防,对人类健康构成了巨大威胁。因此,必须了解H9N2病毒在肠粘膜中的存活和侵袭机制。在这项研究中,我们使用包含肠道隐窝和从肠道干细胞分化而来的绒毛的小鼠三维肠类器官,来探索H9N2禽流感病毒与肠粘膜之间的相互作用。 H9N2病毒的HA,NA,NP和PB1基因可在1小时的肠道类器官中检测到,并在感染后48小时达到峰值。此外,还可以通过免疫荧光在类器官中检测到H9N2病毒的HA和NP蛋白。病毒入侵导致肠道类器官的破坏,Wnt3,Dll1和Dll4的mRNA转录表达降低。肠类器官异常生长可能归因于Paneth细胞的丢失,如lyz1和defcr1的低mRNA转录水平所表明的。这项研究表明,H9N2病毒可以入侵肠道类器官,然后造成损害,并影响肠道干细胞的增殖和分化,从而促进Paneth细胞的损失。

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