MprF-mediated immune evasion is necessary for Lactiplantibacillus plantarum resilience in the Drosophila gut during inflammation.


Journal

PLoS pathogens
ISSN: 1553-7374
Titre abrégé: PLoS Pathog
Pays: United States
ID NLM: 101238921

Informations de publication

Date de publication:
19 Aug 2024
Historique:
received: 07 03 2024
accepted: 30 07 2024
medline: 19 8 2024
pubmed: 19 8 2024
entrez: 19 8 2024
Statut: aheadofprint

Résumé

Multiple peptide resistance factor (MprF) confers resistance to cationic antimicrobial peptides (AMPs) in several pathogens, thereby enabling evasion of the host immune response. The role of MprF in commensals remains, however, uncharacterized. To close this knowledge gap, we used a common gut commensal of animals, Lactiplantibacillus plantarum, and its natural host, the fruit fly Drosophila melanogaster, as an experimental model to investigate the role of MprF in commensal-host interactions. The L. plantarum ΔmprF mutant that we generated exhibited deficiency in the synthesis of lysyl-phosphatidylglycerol (Lys-PG), resulting in increased negative cell surface charge and increased susceptibility to AMPs. Susceptibility to AMPs had no effect on ΔmprF mutant's ability to colonize guts of uninfected flies. However, we observed significantly reduced abundance of the ΔmprF mutant after infection-induced inflammation in the guts of wild-type flies but not flies lacking AMPs. Additionally, we found that the ΔmprF mutant compared to wild-type L. plantarum induces a stronger intestinal immune response in flies due to the increased release of immunostimulatory peptidoglycan fragments, indicating an important role of MprF in promoting host tolerance to commensals. Our further analysis suggests that MprF-mediated lipoteichoic acid modifications are involved in host immunomodulation. Overall, our results demonstrate that MprF, besides its well-characterized role in pathogen immune evasion and virulence, is also an important commensal resilience factor.

Identifiants

pubmed: 39159259
doi: 10.1371/journal.ppat.1012462
pii: PPATHOGENS-D-24-00512
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1012462

Informations de copyright

Copyright: © 2024 Arias-Rojas et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Auteurs

Aranzazu Arias-Rojas (A)

Research group Genetics of host-microbe interactions, Max Planck Institute for Infection Biology, Berlin, Germany.
Department of Biology, Chemistry, and Pharmacy, Freie Universität Berlin, Berlin, Germany.

Adini Q Arifah (AQ)

Helmholtz Institute for RNA-based Infection Research (HIRI), Helmholtz Centre for Infection Research (HZI), Würzburg, Germany.

Georgia Angelidou (G)

Core facility for metabolomics and small molecules mass spectrometry, Max Planck Institute for Terrestrial Microbiology, Marburg, Germany.

Belal Alshaar (B)

Division of Bioanalytical Chemistry, Priority Area Infections, Research Center Borstel, Leibniz Lung Center, Borstel, Germany.

Ursula Schombel (U)

Division of Bioanalytical Chemistry, Priority Area Infections, Research Center Borstel, Leibniz Lung Center, Borstel, Germany.

Emma Forest (E)

Research group Genetics of host-microbe interactions, Max Planck Institute for Infection Biology, Berlin, Germany.
CNRS, Aix-Marseille Univ, LISM UMR7255, IMM FR3479, Marseille, France.
Aix Marseille Université, INSERM, SSA, MCT, Marseille, France.

Dagmar Frahm (D)

Research group Genetics of host-microbe interactions, Max Planck Institute for Infection Biology, Berlin, Germany.

Volker Brinkmann (V)

Microscopy Core Facility, Max Planck Institute for Infection Biology, Berlin, Germany.

Nicole Paczia (N)

Core facility for metabolomics and small molecules mass spectrometry, Max Planck Institute for Terrestrial Microbiology, Marburg, Germany.

Chase L Beisel (CL)

Helmholtz Institute for RNA-based Infection Research (HIRI), Helmholtz Centre for Infection Research (HZI), Würzburg, Germany.
Medical Faculty, University of Würzburg, Würzburg, Germany.

Nicolas Gisch (N)

Division of Bioanalytical Chemistry, Priority Area Infections, Research Center Borstel, Leibniz Lung Center, Borstel, Germany.

Igor Iatsenko (I)

Research group Genetics of host-microbe interactions, Max Planck Institute for Infection Biology, Berlin, Germany.

Classifications MeSH