A mycobacterial Sec61 inhibitor disrupts lysosome function by blocking Vacuolar-ATPase biosynthesis.

Abstract

Mycolactone is the virulence toxin of Mycobacterium ulcerans, causative agent of Buruli ulcer. Mycolactone inhibits the Sec61-dependent co-translational translocation of signal peptide-bearing secreted and membrane proteins into the endoplasmic reticulum. Sec61 inhibition leads to accumulation of mislocalised proteins in the cytosol and initially triggers an integrated stress response-dependent activation of autophagy that contributes to cell survival. Here we show that sustained exposure of cells to mycolactone causes a block in late-stage autophagy and induces nuclear translocation of the lysosomal stress marker TFEB. This coincides with loss of ATP6AP1 and ATP6AP2, Sec61-substrates required for assembly of the Vacuolar-ATPase, leading to reduced lysosomal biogenesis and acidification. This compromises the cells capacity to withstand the proteostatic stress caused by Sec61 inhibition and impairs the ability of phagocytes to combat infection with M. ulcerans. Loss of lysosomal function could contribute to both the tissue necrosis and immunosuppression seen in Buruli ulcer. Furthermore, since Sec61 inhibition is being pursued as a therapeutic target in several diseases, potential drugs should be screened against this activity to avoid unwanted side-effects.