TY - JOUR
T1 - The obligate intracellular bacterium Orientia tsutsugamushi differentiates into a developmentally distinct extracellular state
AU - Atwal, Sharanjeet
AU - Wongsantichon, Jantana
AU - Giengkam, Suparat
AU - Saharat, Kittirat
AU - Pittayasathornthun, Yanin Jaiyen
AU - Chuenklin, Suthida
AU - Wang, Loo Chien
AU - Chung, Taerin
AU - Huh, Hyun
AU - Lee, Sang Hyuk
AU - Sobota, Radoslaw M.
AU - Salje, Jeanne
N1 - Funding Information:
We thank each laboratory member for valuable discussions and support. We are grateful to the following people for providing helpful feedback and insightful comments related to the project and the paper: Jonathan Dworkin from Columbia University, Dave Dubnau from PHRI, and Diana Stafforini from Life Science Editors. We also appreciate the support from Patricia Greenberg and Tracy Andrews at the Rutgers University Biostatistics and Epidemiology Services (RUBIES). This work was funded by a Royal Society Dorothy Hodgkin Research Fellowship (J.S.) (DH140154), a Newton Fund MRC-NSTDA grant (Y.J./J.S.) (MR/N012380/1), and National Institute of Health/National Institute of Allergy and Infectious Diseases grants (R21AI144385 and R56AI148645) (J.S.), A*STAR core funding and Singapore National Research Foundation under its NRF-SIS “SingMass” scheme (R.M.S.), and a US Department of Energy grant (DE-SC0019313) (H.H., T.C.).
Funding Information:
We thank each laboratory member for valuable discussions and support. We are grateful to the following people for providing helpful feedback and insightful comments related to the project and the paper: Jonathan Dworkin from Columbia University, Dave Dubnau from PHRI, and Diana Stafforini from Life Science Editors. We also appreciate the support from Patricia Greenberg and Tracy Andrews at the Rutgers University Biostatistics and Epidemiology Services (RUBIES). This work was funded by a Royal Society Dorothy Hodgkin Research Fellowship (J.S.) (DH140154), a Newton Fund MRC-NSTDA grant (Y.J./J.S.) (MR/N012380/1), and National Institute of Health/National Institute of Allergy and Infectious Diseases grants (R21AI144385 and R56AI148645) (J.S.), A*STAR core funding and Singapore National Research Foundation under its NRF-SIS “SingMass” scheme (R.M.S.), and a US Department of Energy grant (DE-SC0019313) (H.H., T.C.).
Publisher Copyright:
© 2022, The Author(s).
PY - 2022/12
Y1 - 2022/12
N2 - 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.
AB - 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.
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UR - http://www.scopus.com/inward/citedby.url?scp=85132682856&partnerID=8YFLogxK
U2 - 10.1038/s41467-022-31176-9
DO - 10.1038/s41467-022-31176-9
M3 - Article
C2 - 35739103
AN - SCOPUS:85132682856
SN - 2041-1723
VL - 13
JO - Nature communications
JF - Nature communications
IS - 1
M1 - 3603
ER -