Innate host defense mechanisms SAC bacteria by regulating phosphoinositide kinases and phosphatases

Autophagy. 2022 Feb;18(2):452-454. doi: 10.1080/15548627.2021.2002102. Epub 2021 Nov 23.

Abstract

Human genetics and loss-of-function studies revealed a critical role for macroautophagy/autophagy in host defense. The autophagic delivery of intracellular pathogens to lysosomes is a central mechanism of innate immunity; thus, augmentation of host xenophagy represents a promising and powerful approach to combat infections. The precise mechanisms required for autophagosome biogenesis and maturation, however, remain unclear. Using a targeted genetic screen against phosphoinositide kinases and phosphatases, our recent work identified an essential role for the phosphoinositide phosphatase SACM1L/SAC1 in xenophagy. Re-expression of wild-type or catalytically-dead SACM1L in CRISPR knockout cells confirmed that SACM1L enzymatic activity is required to suppress replication of intracellular Salmonella. Time-dependent, quantitative and live confocal imaging demonstrated that SACM1L-deficient cells accumulate phosphatidylinositol-4-phosphate (PtdIns4P) on bacteria-containing autophagosomes, resulting in delayed fusion with degradative lysosomes and reduced bacterial killing. We further discovered that the secreted Salmonella effector protein SteA, which specifically binds PtdIns4P, exacerbates the SACM1L-dependent delay in autophagosomal maturation. These findings reveal a relationship in which the balance between host defense and bacterial survival depends upon autophagosomal membrane composition.

Keywords: Autophagosome; PtdIns4P; SAC1; SACM1L; Salmonella; SteA; phosphatidylinositol-4-phosphate; phosphoinositide phosphatase; selective autophagy; xenophagy.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • 1-Phosphatidylinositol 4-Kinase* / metabolism
  • Autophagosomes / metabolism
  • Autophagy / genetics
  • Bacteria / metabolism
  • Defense Mechanisms
  • Humans
  • Lysosomes / metabolism
  • Phosphoric Monoester Hydrolases* / genetics
  • Phosphoric Monoester Hydrolases* / metabolism
  • Salmonella / metabolism

Substances

  • 1-Phosphatidylinositol 4-Kinase
  • Phosphoric Monoester Hydrolases