tRNA epitranscriptome determines pathogenicity of the opportunistic pathogen Pseudomonas aeruginosa

Author:

Krueger Jonas12,Preusse Matthias3ORCID,Oswaldo Gomez Nicolas3ORCID,Frommeyer Yannick Noah1ORCID,Doberenz Sebastian1ORCID,Lorenz Anne13,Kordes Adrian14,Grobe Svenja15,Müsken Mathias6ORCID,Depledge Daniel P.478ORCID,Svensson Sarah L.9,Weiss Siegfried10,Kaever Volkhard5,Pich Andreas2,Sharma Cynthia M.9ORCID,Ignatova Zoya11ORCID,Häussler Susanne13412ORCID

Affiliation:

1. Institute for Molecular Bacteriology, Center of Clinical and Experimental Infection Research (TWINCORE), a joint venture of the Hannover Medical School and the Helmholtz Center for Infection Research, Hannover 30625, Germany

2. Research Core Unit Proteomics and Institute for Toxicology, Hannover Medical School, Hannover 30625, Germany

3. Department of Molecular Bacteriology, Helmholtz Center for Infection Research, 38124 Braunschweig, Germany

4. Cluster of Excellence “Resolving Infection susceptibility” (RESIST), Hannover Medical School, Hannover 30625, Germany

5. Research Core Unit Metabolomics and Institute of Pharmacology, Hannover Medical School, Hannover 30625, Germany

6. Central Facility for Microscopy, Helmholtz Centre for Infection Research, Braunschweig 38124, Germany

7. Institute of Virology, Hannover Medical School, Hannover 30625, Germany

8. German Center for Infection Research, Partner Site Hannover-Braunschweig, Hannover 30625, Germany

9. Department of Molecular Infection Biology II, Institute of Molecular Infection Biology, University of Würzburg, Würzburg 97080, Germany

10. Institute of Immunology, Medical School Hannover, Hannover 30625, Germany

11. Institute for Biochemistry and Molecular Biology, University Hamburg, 20146, Germany

12. Department of Clinical Microbiology, Copenhagen University Hospital—Rigshospitalet, Copenhagen 2100, Denmark

Abstract

The success of bacterial pathogens depends on the coordinated expression of virulence determinants. Regulatory circuits that drive pathogenesis are complex, multilayered, and incompletely understood. Here, we reveal that alterations in tRNA modifications define pathogenic phenotypes in the opportunistic pathogen Pseudomonas aeruginosa . We demonstrate that the enzymatic activity of GidA leads to the introduction of a carboxymethylaminomethyl modification in selected tRNAs. Modifications at the wobble uridine base (cmnm 5 U 34 ) of the anticodon drives translation of transcripts containing rare codons. Specifically, in P. aeruginosa the presence of GidA-dependent tRNA modifications modulates expression of genes encoding virulence regulators, leading to a cellular proteomic shift toward pathogenic and well-adapted physiological states. Our approach of profiling the consequences of chemical tRNA modifications is general in concept. It provides a paradigm of how environmentally driven tRNA modifications govern gene expression programs and regulate phenotypic outcomes responsible for bacterial adaption to challenging habitats prevailing in the host niche.

Funder

EC | ERC | HORIZON EUROPE European Research Council

Bayerisches Staatsministerium für Wirtschaft und Medien, Energie und Technologie

Deutsche Forschungsgemeinschaft

Hamburg Innovation Grant

Lower Saxony Ministry for Science and Culture

Novo Nordisk Fonden

Publisher

Proceedings of the National Academy of Sciences

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