Polyphosphate uses mTOR, pyrophosphate, and Rho GTPase components to potentiate bacterial survival in Dictyostelium

• Published in: mBio Vol. 14; no. 5; p. e0193923
• Main Authors: Rahman, Ryan J, Rijal, Ramesh, Jing, Shiyu, Chen, Te-An, Ismail, Issam, Gomer, Richard H
• Format: Journal Article
• Language: English
• Published: United States American Society for Microbiology 31.10.2023
• Subjects: bacterial survival; Dictyostelium; Host-Microbial Interactions; phagocytosis; polyphosphate; Research Article; polyphosphate; phagocytosis; Dictyostelium; bacterial survival
• ISSN: 2150-7511; 2150-7511
• DOI: 10.1128/mbio.01939-23

Although most bacteria are quickly killed after phagocytosis by a eukaryotic cell, some pathogenic bacteria escape death after phagocytosis. Pathogenic species secrete polyP, and the polyP is necessary for the bacteria to prevent their killing after phagocytosis. Conversely, exogenous polyP prevents the killing of ingested bacteria that are normally killed after phagocytosis by human macrophages and the eukaryotic microbe . This suggests the possibility that in these cells, a signal transduction pathway is used to sense polyP and prevent killing of ingested bacteria. In this report, we identify key components of the polyP signal transduction pathway in . In cells lacking these components, polyP is unable to inhibit killing of ingested bacteria. The pathway components have orthologs in human cells, and an exciting possibility is that pharmacologically blocking this pathway in human macrophages would cause them to kill ingested pathogens such as .