Impaired Autophagy Flux is Associated with Proinflammatory Microglia Activation Following Japanese Encephalitis Virus Infection

• Published in: Neurochemical research 2020-09, Vol.45 (9), p.2184-2195
• Main Authors: Kumar, Alok, Kalita, J., Sinha, Rohit A., Singh, Gajendra, B, Anjum, Shukla, Mukti, Tiwari, Swasti, Dhole, T. N., Misra, U. K.
• Format: Article
• Language: English
• Subjects: AKT protein; Apoptosis; Autophagy; Biochemistry; Biomarkers; Biomedical and Life Sciences; Biomedicine; Caspase-12; Cathepsin D; Cell activation; Cell Biology; Cell death; Cerebral cortex; Cytokines; DNA damage; Encephalitis; Fluctuations; Flux; Gene expression; Immunohistochemistry; Infections; Inflammation; Inoculation; Interleukin 1; Interleukin 6; Microglia; Mortality; mRNA; Neurochemistry; Neurodegeneration; Neurology; Neurosciences; Original Paper; Phagocytosis; Spectrophotometry; Substrates; Tumor necrosis factor-α; Vector-borne diseases; Viruses; γ-Interferon
• ISSN: 0364-3190; 1573-6903
• DOI: 10.1007/s11064-020-03080-5

Role of autophagy in Japanese encephalitis viral (JEV) infection is not well known. In the present study, we reported the role of autophagy flux in microglia activation, neurobehavioral function and neuronal death using a mouse model of JEV. Markers for autophagy (LC3-II/I, SQSTM1/P62, phos-Akt, phos-AMPK), and neuronal death (cleaved caspase 12, H2Ax, polyubiquitin) were investigated by western blot at 1, 3 and 7 days post inoculation. Cathepsin D was measured in cerebral cotex of JEV infected mice spectrophotometrically. Microglia activation and pro-inflammatory cytokines (IL1β, TNF-α, IFNγ, IL6) were measured by immunohistochemistry, western blot and qPCR analysis. In order to determine the neuroinflammatory changes and autophagy mediated neuronal cell death, BV2-microglia and N2a-neuronal cells were used. Autophagy activation marker LC3-II/I and its substrate SQSTM1/P62 were significantly increased while cathepsin D activity was decreased on day 7 post inoculation in cerebral cortex. Microglia in cortex were activated and showed higher expression of proinflammatory mRNA of IL1β, TNF-α, IFNγ and IL6, with increased DNA damage (H2AX) and neuronal cell death pathways in hippocampus and neurobehavioral dysfunction. Similar observations on JEV infection mediated autophagy flux inhibition and neuronal cell death was found in N2a neuronal cell. Collectively, our study provides evidence on the role of autophagy regulation, microglial activation and neurodegeneration following JEV infection.