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Article Abstract

Long-term persistent viral infections cause substantial morbidity and associated economic losses in human and veterinary contexts. Yet, the mechanisms associated with establishment of persistent infections are poorly elucidated. We investigated immunomodulatory mechanisms associated with clearance versus persistence of foot-and-mouth disease virus (FMDV) in micro-dissected compartments of the bovine nasopharynx by microarray. The use of laser-capture microdissection allowed elucidation of differential gene regulation within distinct anatomic compartments critical to FMDV infection. Analysis of samples from transitional and persistent phases of infection demonstrated significant differences in transcriptome profiles of animals that cleared infection versus those that became persistently infected carriers. Specifically, it was demonstrated that clearance of FMDV from the nasopharyngeal mucosa was associated with upregulation of targets associated with activation of T cell-mediated immunity. Contrastingly, gene regulation in FMDV carriers suggested inhibition of T cell activation and promotion of Th2 polarization. These findings were corroborated by immunofluorescence microscopy which demonstrated relative abundance of CD8 T cells in the nasopharyngeal mucosa in association with clearance of FMDV. The findings presented herein emphasize that a critical balance between Th1 and Th2 -mediated immunity is essential for successful clearance of FMDV infection and should be considered for development of next-generation vaccines and antiviral products.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736604PMC
http://dx.doi.org/10.1038/s41598-017-18112-4DOI Listing

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Article Synopsis
  • The study explores the persistent infection of foot-and-mouth disease virus (FMDV) in ruminants, focusing on differentially expressed genes (DEG) in epithelial cells of FMDV carriers compared to non-carriers.
  • Pathway analysis reveals that changes in these DEGs can impact immune cell trafficking, potentially reducing the recruitment of certain immune cells like neutrophils while increasing macrophage migration, which may contribute to the virus's persistence.
  • The research suggests that under-expression of specific chemokines and the inhibition of immune responses could hinder the ability of the body to clear the virus, providing insights for future studies on FMDV infections.
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