Systems Analysis of Subjects Acutely Infected with Chikungunya Virus
A. Soares-Schanoski, N. Baptista-Cruz, L. A. Castro-Jorge, R. V. Carvalho, C. A. Santos, N. Ros, U. Oliveira, D. D. Costa, C. L. Santos, M. P. Cunha, M. L. Oliveira, J. C. Alves, R. A. Ocea, D. R. Ribeiro, A. N. Goncalves, P. Gonzalez, A. Suhrbier, P. M. Zanotto, I. J. Azevedo, D. S. Zamboni, R. P. Almeida, P. L. Ho, J. Kalil, M. Y. Nishiyama-Jr, H. I. Nakaya
Abstract
The largest ever recorded epidemic of the chikungunya virus (CHIKV) began in 2004 and affected four continents. Acute symptomatic infections are typically associated with the onset of fever and often debilitating polyarthralgia/polyarthritis. In this study, a systems biology approach was used to analyze the blood transcriptomes of adults acutely infected with CHIKV. Gene signatures that were associated with viral RNA amounts and to the onset of symptoms were identified. Among those genes, the putative role of Eukaryotic Initiation Factor (eIF) family genes and apolipoprotein B mRNA editing catalytic polypeptide-like (APOBEC3A) in the CHIKV replication process were displayed. We further compared these signatures with those induced by dengue virus infection and rheumatoid arthritis. Finally, we demonstrated that CHIKV infection in mice induced IL-1 beta production in a mechanism highly dependent on the inflammasome NLRP3 activation. The findings provided valuable insights into the virus-host interactions during the acute phase and could be useful in the investigation of new and effective therapeutic interventions.
02 /Specification & Classification
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