Zika virus replicates in adult human brain tissue and impairs synapses and memory in mice.
Claudia P FigueiredoFernanda G Q Barros-AragãoRômulo L S NerisPaula S FrostCarolina SoaresIsis N O SouzaJulianna D ZeidlerDaniele Coradini ZamberlanVirginia L de SousaAmanda S SouzaAndré Luis A GuimarãesMaria BellioJorge Marcondes de SouzaSoniza V Alves-LeonGilda A NevesHeitor A Paula-NetoNewton Gonçalves CastroFernanda G De FeliceIranaia Assunção MirandaJulia R ClarkeAndrea T Da PoianSergio T FerreiraPublished in: Nature communications (2019)
Neurological complications affecting the central nervous system have been reported in adult patients infected by Zika virus (ZIKV) but the underlying mechanisms remain unknown. Here, we report that ZIKV replicates in human and mouse adult brain tissue, targeting mature neurons. ZIKV preferentially targets memory-related brain regions, inhibits hippocampal long-term potentiation and induces memory impairment in adult mice. TNF-α upregulation, microgliosis and upregulation of complement system proteins, C1q and C3, are induced by ZIKV infection. Microglia are found to engulf hippocampal presynaptic terminals during acute infection. Neutralization of TNF-α signaling, blockage of microglial activation or of C1q/C3 prevent synapse and memory impairment in ZIKV-infected mice. Results suggest that ZIKV induces synapse and memory dysfunction via aberrant activation of TNF-α, microglia and complement. Our findings establish a mechanism by which ZIKV affects the adult brain, and point to the need of evaluating cognitive deficits as a potential comorbidity in ZIKV-infected adults.
Keyphrases
- zika virus
- dengue virus
- working memory
- aedes aegypti
- cerebral ischemia
- rheumatoid arthritis
- inflammatory response
- resting state
- white matter
- high fat diet induced
- poor prognosis
- endothelial cells
- cell proliferation
- childhood cancer
- functional connectivity
- oxidative stress
- intensive care unit
- multiple sclerosis
- spinal cord injury
- wild type
- lipopolysaccharide induced
- adipose tissue
- risk factors
- brain injury
- young adults
- respiratory failure
- long non coding rna
- induced pluripotent stem cells
- mechanical ventilation