Cargando…

A unique bacterial secretion machinery with multiple secretion centers

The Porphyromonas gingivalis type IX secretion system (T9SS) promotes periodontal disease by secreting gingipains and other virulence factors. By in situ cryoelectron tomography, we report that the P. gingivalis T9SS consists of 18 PorM dimers arranged as a large, caged ring in the periplasm. Near t...

Descripción completa

Detalles Bibliográficos
Autores principales: Song, Liqiang, Perpich, John D., Wu, Chenggang, Doan, Thierry, Nowakowska, Zuzanna, Potempa, Jan, Christie, Peter J., Cascales, Eric, Lamont, Richard J., Hu, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9170169/
https://www.ncbi.nlm.nih.gov/pubmed/35471908
http://dx.doi.org/10.1073/pnas.2119907119
_version_ 1784721356234948608
author Song, Liqiang
Perpich, John D.
Wu, Chenggang
Doan, Thierry
Nowakowska, Zuzanna
Potempa, Jan
Christie, Peter J.
Cascales, Eric
Lamont, Richard J.
Hu, Bo
author_facet Song, Liqiang
Perpich, John D.
Wu, Chenggang
Doan, Thierry
Nowakowska, Zuzanna
Potempa, Jan
Christie, Peter J.
Cascales, Eric
Lamont, Richard J.
Hu, Bo
author_sort Song, Liqiang
collection PubMed
description The Porphyromonas gingivalis type IX secretion system (T9SS) promotes periodontal disease by secreting gingipains and other virulence factors. By in situ cryoelectron tomography, we report that the P. gingivalis T9SS consists of 18 PorM dimers arranged as a large, caged ring in the periplasm. Near the outer membrane, PorM dimers interact with a PorKN ring complex of ∼52 nm in diameter. PorMKN translocation complexes of a given T9SS adopt distinct conformations energized by the proton motive force, suggestive of different activation states. At the inner membrane, PorM associates with a cytoplasmic complex that exhibits 12-fold symmetry and requires both PorM and PorL for assembly. Activated motors deliver substrates across the outer membrane via one of eight Sov translocons arranged in a ring. The T9SSs are unique among known secretion systems in bacteria and eukaryotes in their assembly as supramolecular machines composed of apparently independently functioning translocation motors and export pores.
format Online
Article
Text
id pubmed-9170169
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher National Academy of Sciences
record_format MEDLINE/PubMed
spelling pubmed-91701692022-10-26 A unique bacterial secretion machinery with multiple secretion centers Song, Liqiang Perpich, John D. Wu, Chenggang Doan, Thierry Nowakowska, Zuzanna Potempa, Jan Christie, Peter J. Cascales, Eric Lamont, Richard J. Hu, Bo Proc Natl Acad Sci U S A Biological Sciences The Porphyromonas gingivalis type IX secretion system (T9SS) promotes periodontal disease by secreting gingipains and other virulence factors. By in situ cryoelectron tomography, we report that the P. gingivalis T9SS consists of 18 PorM dimers arranged as a large, caged ring in the periplasm. Near the outer membrane, PorM dimers interact with a PorKN ring complex of ∼52 nm in diameter. PorMKN translocation complexes of a given T9SS adopt distinct conformations energized by the proton motive force, suggestive of different activation states. At the inner membrane, PorM associates with a cytoplasmic complex that exhibits 12-fold symmetry and requires both PorM and PorL for assembly. Activated motors deliver substrates across the outer membrane via one of eight Sov translocons arranged in a ring. The T9SSs are unique among known secretion systems in bacteria and eukaryotes in their assembly as supramolecular machines composed of apparently independently functioning translocation motors and export pores. National Academy of Sciences 2022-04-26 2022-05-03 /pmc/articles/PMC9170169/ /pubmed/35471908 http://dx.doi.org/10.1073/pnas.2119907119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Song, Liqiang
Perpich, John D.
Wu, Chenggang
Doan, Thierry
Nowakowska, Zuzanna
Potempa, Jan
Christie, Peter J.
Cascales, Eric
Lamont, Richard J.
Hu, Bo
A unique bacterial secretion machinery with multiple secretion centers
title A unique bacterial secretion machinery with multiple secretion centers
title_full A unique bacterial secretion machinery with multiple secretion centers
title_fullStr A unique bacterial secretion machinery with multiple secretion centers
title_full_unstemmed A unique bacterial secretion machinery with multiple secretion centers
title_short A unique bacterial secretion machinery with multiple secretion centers
title_sort unique bacterial secretion machinery with multiple secretion centers
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9170169/
https://www.ncbi.nlm.nih.gov/pubmed/35471908
http://dx.doi.org/10.1073/pnas.2119907119
work_keys_str_mv AT songliqiang auniquebacterialsecretionmachinerywithmultiplesecretioncenters
AT perpichjohnd auniquebacterialsecretionmachinerywithmultiplesecretioncenters
AT wuchenggang auniquebacterialsecretionmachinerywithmultiplesecretioncenters
AT doanthierry auniquebacterialsecretionmachinerywithmultiplesecretioncenters
AT nowakowskazuzanna auniquebacterialsecretionmachinerywithmultiplesecretioncenters
AT potempajan auniquebacterialsecretionmachinerywithmultiplesecretioncenters
AT christiepeterj auniquebacterialsecretionmachinerywithmultiplesecretioncenters
AT cascaleseric auniquebacterialsecretionmachinerywithmultiplesecretioncenters
AT lamontrichardj auniquebacterialsecretionmachinerywithmultiplesecretioncenters
AT hubo auniquebacterialsecretionmachinerywithmultiplesecretioncenters
AT songliqiang uniquebacterialsecretionmachinerywithmultiplesecretioncenters
AT perpichjohnd uniquebacterialsecretionmachinerywithmultiplesecretioncenters
AT wuchenggang uniquebacterialsecretionmachinerywithmultiplesecretioncenters
AT doanthierry uniquebacterialsecretionmachinerywithmultiplesecretioncenters
AT nowakowskazuzanna uniquebacterialsecretionmachinerywithmultiplesecretioncenters
AT potempajan uniquebacterialsecretionmachinerywithmultiplesecretioncenters
AT christiepeterj uniquebacterialsecretionmachinerywithmultiplesecretioncenters
AT cascaleseric uniquebacterialsecretionmachinerywithmultiplesecretioncenters
AT lamontrichardj uniquebacterialsecretionmachinerywithmultiplesecretioncenters
AT hubo uniquebacterialsecretionmachinerywithmultiplesecretioncenters