The obligate intracellular bacterium Orientia tsutsugamushi differentiates into a developmentally distinct extracellular state.
Journal
Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555
Informations de publication
Date de publication:
23 06 2022
23 06 2022
Historique:
received:
22
04
2021
accepted:
03
06
2022
entrez:
23
6
2022
pubmed:
24
6
2022
medline:
28
6
2022
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 35739103
doi: 10.1038/s41467-022-31176-9
pii: 10.1038/s41467-022-31176-9
pmc: PMC9226355
doi:
Substances chimiques
Membrane Proteins
0
Peptidoglycan
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S.
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
3603Subventions
Organisme : Medical Research Council
ID : MR/N012380/1
Pays : United Kingdom
Organisme : NIAID NIH HHS
ID : R56 AI148645
Pays : United States
Organisme : NIAID NIH HHS
ID : R21 AI144385
Pays : United States
Informations de copyright
© 2022. The Author(s).
Références
Nat Rev Microbiol. 2017 Sep;15(9):544-558
pubmed: 28626230
Nat Rev Microbiol. 2016 Jun;14(6):385-400
pubmed: 27108705
J Microbiol Methods. 2020 Feb;169:105812
pubmed: 31862457
Mol Microbiol. 2018 Jan;107(2):142-163
pubmed: 29178391
Nat Commun. 2020 Jul 3;11(1):3363
pubmed: 32620750
Comp Funct Genomics. 2008;:623145
pubmed: 18528528
Opt Express. 2014 Jun 30;22(13):15982-91
pubmed: 24977854
Nat Rev Microbiol. 2010 May;8(5):328-39
pubmed: 20372158
PLoS Negl Trop Dis. 2018 Jun 6;12(6):e0006566
pubmed: 29874223
Microb Pathog. 2004 Apr;36(4):219-25
pubmed: 15001228
Annu Rev Genet. 2016 Nov 23;50:423-445
pubmed: 27893963
Nat Commun. 2014 Apr 08;5:3578
pubmed: 24709914
Infect Immun. 2006 Jul;74(7):4246-53
pubmed: 16790799
Science. 2008 Feb 8;319(5864):810-3
pubmed: 18174397
J Infect Dis. 2008 Jul 15;198(2):250-7
pubmed: 18500929
PLoS Negl Trop Dis. 2015 Mar 13;9(3):e0003585
pubmed: 25768004
Nat Rev Microbiol. 2021 Jun;19(6):375-390
pubmed: 33564174
PLoS Negl Trop Dis. 2015 Aug 14;9(8):e0003971
pubmed: 26274584
Infect Immun. 1980 Oct;30(1):231-43
pubmed: 6777300
PLoS Negl Trop Dis. 2015 Aug 28;9(8):e0004009
pubmed: 26317517
Infect Immun. 2011 Apr;79(4):1718-27
pubmed: 21282412
Mol Microbiol. 2017 Aug;105(3):440-452
pubmed: 28513097
Opt Express. 2018 Apr 2;26(7):8049-8058
pubmed: 29715778
Cell. 2016 Oct 20;167(3):670-683.e10
pubmed: 27768890
Infect Immun. 1985 Dec;50(3):603-9
pubmed: 2415453
Infect Immun. 2010 May;78(5):1915-23
pubmed: 20160019
Nucleic Acids Res. 2017 Jan 4;45(D1):D1107-D1111
pubmed: 27899654
Trop Med Infect Dis. 2018 Jan 17;3(1):
pubmed: 30274407
Nat Rev Microbiol. 2021 Apr;19(4):256-271
pubmed: 33149273