TY - JOUR
T1 - Powassan Virus Induces Structural Changes in Human Neuronal Cells In Vitro and Murine Neurons In Vivo
AU - Nelson, Jacob
AU - Ochoa, Lorenzo
AU - Villareal, Paula
AU - Dunn, Tiffany
AU - Wu, Ping
AU - Vargas, Gracie
AU - Freiberg, Alexander N.
N1 - Funding Information:
This research was supported in part by grant UL1TR000071 from the National Center for Advancing Translational Sciences, National Institutes of Health, by the Institute for Human Infections and Immunity (G.V. and A.N.F.), through a pilot project grant of the Institute of Human Infections and Immunity (P.W. and A.N.F.), as well as departmental funds (A.N.F.), and by the training fellowship for Lorenzo Ochoa (Funding for LO NIEHS-T32ES007254).
Publisher Copyright:
© 2022 by the authors.
PY - 2022/10
Y1 - 2022/10
N2 - Powassan virus (POWV) is a tick-borne flavivirus (TBFV) that can cause severe encephalitis in humans with a case–fatality rate as high as 11%. Patients who survive severe encephalitic disease can develop long-term neurological sequelae that can be debilitating and life-long. In this study, we have sought to characterize a primary human fetal brain neural stem cell system (hNSC), which can be differentiated into neuron and astrocyte co-cultures, to serve as a translational in vitro system for infection with POWV and a comparative mosquito-borne flavivirus (MBFV), West Nile virus (WNV). We found that both viruses are able to infect both cell types in the co-culture and that WNV elicits a strong inflammatory response characterized by increased cytokines IL-4, IL-6, IL-8, TNF-α and IL-1β and activation of apoptosis pathways. POWV infection resulted in fewer cytokine responses, as well as less detectable apoptosis, while neurons infected with POWV exhibited structural aberrations forming in the dendrites. These anomalies are consistent with previous findings in which tick-borne encephalitis virus (TBEV) infected murine primary neurons formed laminal membrane structures (LMS). Furthermore, these structural aberrations are also recapitulated in brain tissue from infected mice. Our findings indicate that POWV is capable of infecting human primary neurons and astrocytes without causing apparent widespread apoptosis, while forming punctate structures reminiscent with LMS in primary human neurons and in vivo.
AB - Powassan virus (POWV) is a tick-borne flavivirus (TBFV) that can cause severe encephalitis in humans with a case–fatality rate as high as 11%. Patients who survive severe encephalitic disease can develop long-term neurological sequelae that can be debilitating and life-long. In this study, we have sought to characterize a primary human fetal brain neural stem cell system (hNSC), which can be differentiated into neuron and astrocyte co-cultures, to serve as a translational in vitro system for infection with POWV and a comparative mosquito-borne flavivirus (MBFV), West Nile virus (WNV). We found that both viruses are able to infect both cell types in the co-culture and that WNV elicits a strong inflammatory response characterized by increased cytokines IL-4, IL-6, IL-8, TNF-α and IL-1β and activation of apoptosis pathways. POWV infection resulted in fewer cytokine responses, as well as less detectable apoptosis, while neurons infected with POWV exhibited structural aberrations forming in the dendrites. These anomalies are consistent with previous findings in which tick-borne encephalitis virus (TBEV) infected murine primary neurons formed laminal membrane structures (LMS). Furthermore, these structural aberrations are also recapitulated in brain tissue from infected mice. Our findings indicate that POWV is capable of infecting human primary neurons and astrocytes without causing apparent widespread apoptosis, while forming punctate structures reminiscent with LMS in primary human neurons and in vivo.
KW - clarity
KW - human neural stem cell (hNSC)-derived neuron astrocyte co-culture
KW - laminal membrane structures
KW - neuroinflammation
KW - neurovirulence
KW - powassan virus
KW - west nile virus
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U2 - 10.3390/pathogens11101218
DO - 10.3390/pathogens11101218
M3 - Article
C2 - 36297275
AN - SCOPUS:85140458746
SN - 2076-0817
VL - 11
JO - Pathogens
JF - Pathogens
IS - 10
M1 - 1218
ER -