tRNA epitranscriptome determines pathogenicity of the opportunistic pathogen Pseudomonas aeruginosa .
Jonas KruegerMatthias PreusseNicolas Oswaldo GomezYannick Noah FrommeyerSebastian DoberenzAnne LorenzAdrian KordesSvenja GrobeMathias MüskenDaniel P DepledgeSarah L SvenssonSiegfried WeissVolkhard KaeverAndreas PichCynthia Mira SharmaZoya IgnatovaSusanne HäußlerPublished in: Proceedings of the National Academy of Sciences of the United States of America (2024)
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.
Keyphrases
- pseudomonas aeruginosa
- biofilm formation
- gene expression
- cystic fibrosis
- poor prognosis
- candida albicans
- escherichia coli
- antimicrobial resistance
- genome wide
- staphylococcus aureus
- acinetobacter baumannii
- transcription factor
- dna methylation
- single cell
- public health
- binding protein
- type diabetes
- adipose tissue
- metabolic syndrome
- multidrug resistant
- hydrogen peroxide
- nitric oxide
- skeletal muscle
- genome wide analysis
- genome wide identification
- label free