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The Central Role of IFI204 in IFN-β Release and Autophagy Activation during Mycobacterium bovis Infection

Journal

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fcimb.2017.00169

Keywords

IFI204; IFN-beta; M. bovis; autophagy; DNA sensor

Funding

  1. MoSTRCUK international cooperation project [2013DFG32500]
  2. National Natural Science Foundation of China [31572487]
  3. State Key Lab of Agrobiotechnology [2012SKLAB06-14]
  4. CAU Foreign Experts Major Projects [2012z018]
  5. 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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