摘要：SummaryEnteroviruses, particularly the group B coxsackieviruses (CVBs), have been associated with the development of type 1 diabetes. Several CVB serotypes establish chronic infections in human cellsin vivoandin vitro. However, the mechanisms leading to enterovirus persistency and, possibly, beta cell autoimmunity are not fully understood. We established a carrier-state-type persistent infection model in human pancreatic cell line PANC-1 using two distinct CVB1 strains and profiled the infection-induced changes in cellular transcriptome. In the current study, we observed clear changes in the gene expression of factors associated with the pancreatic microenvironment, the secretory pathway, and lysosomal biogenesis during persistent CVB1 infections. Moreover, we found that the antiviral response pathways were activated differently by the two CVB1 strains. Overall, our study reveals extensive transcriptional responses in persistently CVB1-infected pancreatic cells with strong opposite but also common changes between the two strains.Graphical abstractDisplay OmittedHighlights•Establishment of persistent CVB1 infection in PANC-1 cells using two CVB1 strains•Extensive transcriptional responses in persistently CVB1-infected pancreatic cells•Changes in pancreatic microenvironment, secretory pathway, and lysosomes•Antiviral immune response was activated differently by the two CVB1 strainsVirology; Cell biology; Transcriptomics
