Staphylococcus aureus Lpl protein triggers human host cell invasion via activation of Hsp90 receptor.


Journal

Cellular microbiology
ISSN: 1462-5822
Titre abrégé: Cell Microbiol
Pays: India
ID NLM: 100883691

Informations de publication

Date de publication:
01 2020
Historique:
received: 11 06 2019
revised: 02 08 2019
accepted: 26 08 2019
pubmed: 14 9 2019
medline: 10 4 2021
entrez: 14 9 2019
Statut: ppublish

Résumé

Staphylococcus aureus is a facultative intracellular pathogen. Recently, it has been shown that the protein part of the lipoprotein-like lipoproteins (Lpls), encoded by the lpl cluster comprising of 10 lpls paralogue genes, increases pathogenicity, delays the G2/M phase transition, and also triggers host cell invasion. Here, we show that a recombinant Lpl1 protein without the lipid moiety binds directly to the isoforms of the human heat shock proteins Hsp90α and Hsp90ß. Synthetic peptides covering the Lpl1 sequence caused a twofold to fivefold increase of S. aureus invasion in HaCaT cells. Antibodies against Hsp90 decrease S. aureus invasion in HaCaT cells and in primary human keratinocytes. Additionally, inhibition of ATPase function of Hsp90 or silencing Hsp90α expression by siRNA also decreased the S. aureus invasion in HaCaT cells. Although the Hsp90ß is constitutively expressed, the Hsp90α isoform is heat-inducible and appears to play a major role in Lpl1 interaction. Pre-incubation of HaCaT cells at 39°C increased both the Hsp90α expression and S. aureus invasion. Lpl1-Hsp90 interaction induces F-actin formation, thus, triggering an endocytosis-like internalisation. Here, we uncovered a new host cell invasion principle on the basis of Lpl-Hsp90 interaction.

Identifiants

pubmed: 31515903
doi: 10.1111/cmi.13111
doi:

Substances chimiques

Actins 0
Bacterial Proteins 0
HSP90 Heat-Shock Proteins 0
HSP90AA2P protein, human 0
HSP90AB1 protein, human 0
Lipoproteins 0
Recombinant Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13111

Informations de copyright

© 2019 The Authors. Cellular Microbiology published by John Wiley & Sons Ltd.

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Auteurs

Paula M Tribelli (PM)

Microbial Genetics, Interfaculty Institute of Microbiology and Infection Medicine Tübingen (IMIT), University of Tübingen, Tübingen, Germany.
Departamento de Química Biológica, FCEyN-UBA, Buenos Aires, Argentina.
IQUIBICEN-CONICET, Buenos Aires, Argentina.

Arif Luqman (A)

Microbial Genetics, Interfaculty Institute of Microbiology and Infection Medicine Tübingen (IMIT), University of Tübingen, Tübingen, Germany.
Institut Teknologi Sepuluh Nopember, Biology Department, Surabaya, Indonesia.

Minh-Thu Nguyen (MT)

Microbial Genetics, Interfaculty Institute of Microbiology and Infection Medicine Tübingen (IMIT), University of Tübingen, Tübingen, Germany.
Division of Microbiology, Paul-Ehrlich Institute, Langen, Germany.

Johannes Madlung (J)

Proteome Center Tübingen, University of Tübingen, Tübingen, Germany.

Sook-Ha Fan (SH)

Microbial Genetics, Interfaculty Institute of Microbiology and Infection Medicine Tübingen (IMIT), University of Tübingen, Tübingen, Germany.

Boris Macek (B)

Proteome Center Tübingen, University of Tübingen, Tübingen, Germany.

Peter Sass (P)

Microbial Bioactive Compounds, Interfaculty Institute of Microbiology and Infection Medicine Tübingen (IMIT), University of Tübingen, Tübingen, Germany.

Katharina Bitschar (K)

Department of Dermatology, University of Tübingen, Tübingen, Germany.

Birgit Schittek (B)

Department of Dermatology, University of Tübingen, Tübingen, Germany.

Dorothee Kretschmer (D)

Department of Infection Biology, Interfaculty Institute for Microbiology and Infection Medicine Tübingen (IMIT), University of Tübingen, Tübingen, Germany.

Friedrich Götz (F)

Microbial Genetics, Interfaculty Institute of Microbiology and Infection Medicine Tübingen (IMIT), University of Tübingen, Tübingen, Germany.

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