Login / Signup

Oxidization of TGFβ-activated kinase by MPT53 is required for immunity to Mycobacterium tuberculosis.

Lin WangZhonghua LiuJie WangTiansheng ZhengJuehui WuTianqi TangHaohao LiHua YangLianhua QinDapeng MaJianxia ChenFeng LiuPeng WangRuijuan ZhengPeng SongYilong ZhouZhenling CuiXiangyang WuXiaochen HuangHaijiao LiangShanshan ZhangJingjing CaoChunyan WuYiping ChenDan SuXinchun ChenGucheng ZengBaoxue Ge
Published in: Nature microbiology (2019)
Mycobacterium tuberculosis (Mtb)-derived components are usually recognized by pattern recognition receptors to initiate a cascade of innate immune responses. One striking characteristic of Mtb is their utilization of different type VII secretion systems to secrete numerous proteins across their hydrophobic and highly impermeable cell walls, but whether and how these Mtb-secreted proteins are sensed by host immune system remains largely unknown. Here, we report that MPT53 (Rv2878c), a secreted disulfide-bond-forming-like protein of Mtb, directly interacts with TGF-β-activated kinase 1 (TAK1) and activates TAK1 in a TLR2- or MyD88-independent manner. MPT53 induces disulfide bond formation at C210 on TAK1 to facilitate its interaction with TRAFs and TAB1, thus activating TAK1 to induce the expression of pro-inflammatory cytokines. Furthermore, MPT53 and its disulfide oxidoreductase activity is required for Mtb to induce the host inflammatory responses via TAK1. Our findings provide an alternative pathway for host signalling proteins to sense Mtb infection and may favour the improvement of current vaccination strategies.
Keyphrases