Increased IL-6 Levels and the Upregulation of Iron Regulatory Biomarkers Contribute to the Progression of Japanese Encephalitis Virus Infection’s Pathogenesis

• Published in: Neuromolecular medicine Vol. 25; no. 4; pp. 596 - 602
• Main Authors: Singh, Anjali, Ghildiyal, Sneha, Mishra, Prabhaker, Singh, Gajendra, Dandu, Himanshu, Kumar, Alok
• Format: Journal Article
• Language: English
• Published: New York Springer US 01.12.2023; Springer Nature B.V
• Subjects: Biomarkers; Biomedical and Life Sciences; Biomedicine; Disease Progression; Encephalitis; Encephalitis Virus, Japanese - genetics; Encephalitis Virus, Japanese - metabolism; Encephalitis, Japanese - genetics; Encephalitis, Japanese - metabolism; Genetic diversity; Genotypes; Hepcidin; Homeostasis; Humans; Infections; Inflammation; Interleukin 6; Interleukin-6 - genetics; Interleukin-6 - metabolism; Internal Medicine; Iron; Iron - metabolism; Meningoencephalitis; Neurology; Neurosciences; Risk groups; Transferrins; Transferrins - genetics; Transferrins - metabolism; Up-Regulation; Japanese encephalitis virus infection; Transferrin; Hepcidin; Transferrin receptors; IL-6
• ISSN: 1535-1084; 1559-1174
• DOI: 10.1007/s12017-023-08762-1

Integrated analysis of iron regulatory biomarkers and inflammatory response could be an important strategy for Japanese encephalitis viral (JEV) infection disease management. In the present study, the inflammatory response was assessed by measuring serum Interleukin-6 (IL-6) levels using ELISA, and the transcription levels of iron homeostasis regulators were analyzed via RT-PCR. Furthermore, inter-individual variation in the transferrin gene was analyzed by PCR–RFLP and their association with clinical symptoms, susceptibility, severity, and outcomes was assessed through binary logistic regression and classification and regression tree (CART) analysis. Our findings revealed elevated levels of IL-6 in serum as well as increased expression of hepcidin (HAMP), transferrin (TF), and transferrin receptor-1 (TFR1) mRNA in JEV infection cases. Moreover, we found a genetic variation in TF (rs4481157) associated with clinical symptoms of meningoencephalitis. CART analysis indicates that individuals with the wild-type TF genotype are more susceptible to moderate JEV infection, while those with the homozygous type are in the high-risk group to develop a severe JEV condition. In summary, the study highlights that JEV infection induces alteration in both IL-6 levels and iron regulatory processes, which play pivotal roles in the development of JEV disease pathologies.