tetano
Editor, Senior Moderator
Vet Res. 2017 Nov 2;48(1):71. doi: 10.1186/s13567-017-0478-6.
[h=1]Crosstalk between H9N2 avian influenza virus and crypt-derived intestinal organoids.[/h] Huang L[SUP]1[/SUP], Hou Q[SUP]1[/SUP], Ye L[SUP]1[/SUP], Yang Q[SUP]1[/SUP], Yu Q[SUP]2[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] 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.
PMID: 29096712 DOI: 10.1186/s13567-017-0478-6
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[h=1]Crosstalk between H9N2 avian influenza virus and crypt-derived intestinal organoids.[/h] Huang L[SUP]1[/SUP], Hou Q[SUP]1[/SUP], Ye L[SUP]1[/SUP], Yang Q[SUP]1[/SUP], Yu Q[SUP]2[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] 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.
PMID: 29096712 DOI: 10.1186/s13567-017-0478-6
Free full text