TY - JOUR
T1 - tRNA epitranscriptome determines pathogenicity of the opportunistic pathogen Pseudomonas aeruginosa
AU - Krueger, Jonas
AU - Preusse, Matthias
AU - Oswaldo Gomez, Nicolas
AU - Frommeyer, Yannick Noah
AU - Doberenz, Sebastian
AU - Lorenz, Anne
AU - Kordes, Adrian
AU - Grobe, Svenja
AU - Müsken, Mathias
AU - Depledge, Daniel P
AU - Svensson, Sarah L
AU - Weiss, Siegfried
AU - Kaever, Volkhard
AU - Pich, Andreas
AU - Sharma, Cynthia M
AU - Ignatova, Zoya
AU - Häussler, Susanne
PY - 2024/3/12
Y1 - 2024/3/12
N2 - 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 (cmnm5U34) 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.
AB - 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 (cmnm5U34) 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.
UR - http://www.scopus.com/inward/record.url?scp=85187171255&partnerID=8YFLogxK
U2 - 10.1073/pnas.2312874121
DO - 10.1073/pnas.2312874121
M3 - Journal article
C2 - 38451943
SN - 0027-8424
VL - 121
SP - e2312874121
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 11
M1 - e2312874121
ER -