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Abstract
Orientia tsutsugamushi (Ot) is an obligate intracellular bacterium in the family Rickettsiaceae that causes scrub typhus, a severe mite-borne human disease. Its mechanism of cell exit is unusual amongst Rickettsiaceae, as Ot buds off the surface of infected cells enveloped in plasma membrane. Here, we show that Ot bacteria that have budded out of host cells are in a distinct developmental stage compared with intracellular bacteria. We refer to these two stages as intracellular and extracellular bacteria (IB and EB, respectively). These two forms differ in physical properties: IB is both round and elongated, and EB is round. Additionally, IB has higher levels of peptidoglycan and is physically robust compared with EB. The two bacterial forms differentially express proteins involved in bacterial physiology and host-pathogen interactions, specifically those involved in bacterial dormancy and stress response, and outer membrane autotransporter proteins ScaA and ScaC. Whilst both populations are infectious, entry of IB Ot is sensitive to inhibitors of both clathrin-mediated endocytosis and macropinocytosis, whereas entry of EB Ot is only sensitive to a macropinocytosis inhibitor. Our identification and detailed characterization of two developmental forms of Ot significantly advances our understanding of the intracellular lifecycle of an important human pathogen.
Orientia tsutsugamushi (Ot) the causing agent of scrub typhus exits infected cells using a unique mechanism that involves budding off the surface of infected cells. Here, Atwal et al. report that Ots that have budded from their host cells are in a distinct developmental stage than intracellular bacteria and provide the first characterization of this extracellular stage. Both forms are infectious but differ in their physical properties, proteome, and entry mechanism into host cells.
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1 Rutgers the State University of New Jersey, Public Health Research Institute, Newark, USA (GRID:grid.430387.b) (ISNI:0000 0004 1936 8796)
2 Mahidol University, Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Bangkok, Thailand (GRID:grid.10223.32) (ISNI:0000 0004 1937 0490)
3 Rutgers the State University of New Jersey, Public Health Research Institute, Newark, USA (GRID:grid.430387.b) (ISNI:0000 0004 1936 8796); Mahidol University, Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Bangkok, Thailand (GRID:grid.10223.32) (ISNI:0000 0004 1937 0490)
4 Technology and Research (A*STAR), Functional Proteomics Laboratory, Institute of Molecular and Cell Biology, Agency for Science, Singapore, Singapore (GRID:grid.185448.4) (ISNI:0000 0004 0637 0221); Technology and Research (A*STAR), SingMass—National Mass Spectrometry Laboratory, Institute of Molecular and Cell Biology, Agency for Science, Singapore, Singapore (GRID:grid.185448.4) (ISNI:0000 0004 0637 0221)
5 Rutgers University, Institute for Quantitative Biomedicine, Piscataway, USA (GRID:grid.430387.b) (ISNI:0000 0004 1936 8796)
6 Rutgers University, Institute for Quantitative Biomedicine, Piscataway, USA (GRID:grid.430387.b) (ISNI:0000 0004 1936 8796); Rutgers University, Department of Physics and Astronomy, Piscataway, USA (GRID:grid.430387.b) (ISNI:0000 0004 1936 8796)
7 Rutgers the State University of New Jersey, Public Health Research Institute, Newark, USA (GRID:grid.430387.b) (ISNI:0000 0004 1936 8796); Mahidol University, Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Bangkok, Thailand (GRID:grid.10223.32) (ISNI:0000 0004 1937 0490); University of Oxford, Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, Oxford, UK (GRID:grid.4991.5) (ISNI:0000 0004 1936 8948)