Fundamental properties of the mammalian innate immune system revealed by multispecies comparison of type I interferon responses.

• Main Authors: Andrew E Shaw, Joseph Hughes, Quan Gu, Abdelkader Behdenna, Joshua B Singer, Tristan Dennis, Richard J Orton, Mariana Varela, Robert J Gifford, Sam J Wilson, Massimo Palmarini
• Format: Article
• Language: English
• Published: Public Library of Science (PLoS) 2017-12-01
• Series: PLoS Biology
• Online Access: https://doi.org/10.1371/journal.pbio.2004086
• ISSN: 1544-9173; 1545-7885

The host innate immune response mediated by type I interferon (IFN) and the resulting up-regulation of hundreds of interferon-stimulated genes (ISGs) provide an immediate barrier to virus infection. Studies of the type I 'interferome' have mainly been carried out at a single species level, often lacking the power necessary to understand key evolutionary features of this pathway. Here, using a single experimental platform, we determined the properties of the interferomes of multiple vertebrate species and developed a webserver to mine the dataset. This approach revealed a conserved 'core' of 62 ISGs, including genes not previously associated with IFN, underscoring the ancestral functions associated with this antiviral host response. We show that gene expansion contributes to the evolution of the IFN system and that interferomes are shaped by lineage-specific pressures. Consequently, each mammal possesses a unique repertoire of ISGs, including genes common to all mammals and others unique to their specific species or phylogenetic lineages. An analysis of genes commonly down-regulated by IFN suggests that epigenetic regulation of transcription is a fundamental aspect of the IFN response. Our study provides a resource for the scientific community highlighting key paradigms of the type I IFN response.