Journal
FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY
Volume 7, Issue -, Pages -Publisher
FRONTIERS MEDIA SA
DOI: 10.3389/fcimb.2017.00169
Keywords
IFI204; IFN-beta; M. bovis; autophagy; DNA sensor
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Funding
- MoSTRCUK international cooperation project [2013DFG32500]
- National Natural Science Foundation of China [31572487]
- State Key Lab of Agrobiotechnology [2012SKLAB06-14]
- CAU Foreign Experts Major Projects [2012z018]
- High-end Foreign Experts Recruitment Program [GDW20151100036]
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Mycobacterium bovis (M. bovis) is the pathogen of animals and humans that can replicate in the phagosomes of myeloid cells. Cytosolic detection of bacterial products plays a crucial role in initiating the innate immune response, including autophagy activation and interferon-beta (IFN-beta) release. Although IFN-beta release and autophagy activation have been reported during mycobacterium infection, the mechanisms underlying remains poorly defined. Here, we demonstrated that IFN-beta release increases in macrophages exposed to M. bovis and this requires the activation of the DNA sensor of interferon-gamma inducible protein 204 (IFI204). Knockdown of the IFI204 in immortalized and primary murine macrophages blocked IFN-beta production and autophagy marker LC3 expression. Thus, our results indicate that the IFI204 is an important sensor for innate immune responses of M. bovis infection.
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