Differential effects of Usutu and West Nile viruses on neuroinflammation, immune cell recruitment and blood-brain barrier integrity.
Orianne ConstantGhizlane MaarifiJonathan BarthelemyMarie-France MartinBachirou TintoGiovanni SaviniPhilippe Van de PerreSébastien NisoleYannick SimoninSara SalinasPublished in: Emerging microbes & infections (2022)
Usutu (USUV) and West Nile (WNV) viruses are two closely related Flavivirus belonging to Japanese encephalitis virus serogroup. Evidence of increased circulation of these two arbovirus now exist in Europe with neurological disorders reported in humans mainly for WNV, despite that the interaction and effects of viral infections on the neurovasculature are poorly described, notably for USUV. Using a human in vitro blood-brain barrier (BBB) and a mouse model, this study characterizes and compares the cerebral endothelial cell permissiveness, innate immunity and inflammatory responses and immune cell recruitment during infection by USUV and WNV. Both viruses are able to infect and cross the human BBB but with different consequences. We observed that WNV infect BBB cells resulting in significant endothelium dysregulation, potent neuroinflammation and immune cell recruitment, in agreement with previous studies. USUV, despite being able to infect BBB cells with higher replication rate than WNV, does not strongly affect endothelium integrity. Importantly, USUV also induces neuroinflammation, immune cell recruitment such as T lymphocytes, monocytes and dendritic cells (DCs) and was able to infect dendritic cells (DCs) more efficiently compared to WNV with greater propensity for BBB recruitment. DCs may have differential roles for neuroinvasion of the two related viruses.
Keyphrases
- blood brain barrier
- cerebral ischemia
- dendritic cells
- endothelial cells
- induced apoptosis
- cell cycle arrest
- mouse model
- lipopolysaccharide induced
- traumatic brain injury
- immune response
- nitric oxide
- lps induced
- cognitive impairment
- sars cov
- induced pluripotent stem cells
- cell death
- oxidative stress
- pluripotent stem cells
- genetic diversity
- inflammatory response
- signaling pathway
- pi k akt
- zika virus
- cell proliferation
- high glucose
- brain injury
- case control
- peripheral blood