tetano
Editor, Senior Moderator
J Infect Dis. 2018 Jan 10. doi: 10.1093/infdis/jiy003. [Epub ahead of print]
[h=1]1918 H1N1 influenza virus replicates and induces pro-inflammatory cytokine responses in extra-respiratory tissues of ferrets.[/h] de Wit E[SUP]1[/SUP], Siegers J[SUP]2[/SUP], Cronin JM[SUP]1[/SUP], Weatherman S[SUP]1[/SUP], van den Brand J[SUP]2[/SUP], Leijten LM[SUP]2[/SUP], van Run P[SUP]2[/SUP], Begeman L[SUP]2[/SUP], van den Ham HJ[SUP]2[/SUP], Andeweg AC[SUP]2[/SUP], Bushmaker T[SUP]1[/SUP], Scott DP[SUP]3[/SUP], Saturday G[SUP]3[/SUP], Munster VJ[SUP]1[/SUP], Feldmann H[SUP]1[/SUP], van Riel D[SUP]2[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] [h=4]Background:[/h] The 1918 Spanish H1N1 influenza pandemic was the most severe recorded influenza pandemic with an estimated 20-50 million deaths worldwide. Even though it is known that influenza viruses can cause extra-respiratory tract complications-which are often severe or even fatal- the potential contribution of extra-respiratory tissues to the pathogenesis of 1918 H1N1 virus infection has not been studied comprehensively.
[h=4]Methods:[/h] Here, we performed a time course study in ferrets inoculated intranasally with 1918 H1N1 virus, with special emphasis on the involvement of extra-respiratory tissues. Respiratory and extra-respiratory tissues were collected after inoculation for virological, histological and immunological analysis.
[h=4]Results:[/h] Infectious virus was detected at high titers in respiratory tissues, and-at lower titers-in most extra-respiratory tissues. Evidence for active virus replication, as indicated by the detection of nucleoprotein by immunohistochemistry, was observed in the respiratory tract, peripheral and central nervous system, and liver. Pro-inflammatory cytokines were upregulated in respiratory tissues, olfactory bulb, spinal cord, liver, heart and pancreas.
[h=4]Conclusions:[/h] 1918 H1N1 virus spread to, and induced cytokine responses in tissues outside the respiratory tract, which likely contributed to the severity of infection. Moreover, our data support the suggested link between 1918 H1N1 infection and CNS disease.
[h=4]KEYWORDS:[/h] 1918 H1N1 virus; CNS disease; animal model; cytokine; extra-respiratory; ferret model; inflamma; influenza A virus; pathogenesis
PMID: 29329410 DOI: 10.1093/infdis/jiy003
[h=1]1918 H1N1 influenza virus replicates and induces pro-inflammatory cytokine responses in extra-respiratory tissues of ferrets.[/h] de Wit E[SUP]1[/SUP], Siegers J[SUP]2[/SUP], Cronin JM[SUP]1[/SUP], Weatherman S[SUP]1[/SUP], van den Brand J[SUP]2[/SUP], Leijten LM[SUP]2[/SUP], van Run P[SUP]2[/SUP], Begeman L[SUP]2[/SUP], van den Ham HJ[SUP]2[/SUP], Andeweg AC[SUP]2[/SUP], Bushmaker T[SUP]1[/SUP], Scott DP[SUP]3[/SUP], Saturday G[SUP]3[/SUP], Munster VJ[SUP]1[/SUP], Feldmann H[SUP]1[/SUP], van Riel D[SUP]2[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] [h=4]Background:[/h] The 1918 Spanish H1N1 influenza pandemic was the most severe recorded influenza pandemic with an estimated 20-50 million deaths worldwide. Even though it is known that influenza viruses can cause extra-respiratory tract complications-which are often severe or even fatal- the potential contribution of extra-respiratory tissues to the pathogenesis of 1918 H1N1 virus infection has not been studied comprehensively.
[h=4]Methods:[/h] Here, we performed a time course study in ferrets inoculated intranasally with 1918 H1N1 virus, with special emphasis on the involvement of extra-respiratory tissues. Respiratory and extra-respiratory tissues were collected after inoculation for virological, histological and immunological analysis.
[h=4]Results:[/h] Infectious virus was detected at high titers in respiratory tissues, and-at lower titers-in most extra-respiratory tissues. Evidence for active virus replication, as indicated by the detection of nucleoprotein by immunohistochemistry, was observed in the respiratory tract, peripheral and central nervous system, and liver. Pro-inflammatory cytokines were upregulated in respiratory tissues, olfactory bulb, spinal cord, liver, heart and pancreas.
[h=4]Conclusions:[/h] 1918 H1N1 virus spread to, and induced cytokine responses in tissues outside the respiratory tract, which likely contributed to the severity of infection. Moreover, our data support the suggested link between 1918 H1N1 infection and CNS disease.
[h=4]KEYWORDS:[/h] 1918 H1N1 virus; CNS disease; animal model; cytokine; extra-respiratory; ferret model; inflamma; influenza A virus; pathogenesis
PMID: 29329410 DOI: 10.1093/infdis/jiy003