Bacteriophage Infection of the Marine Bacterium Shewanella glacialimarina Induces Dynamic Changes in tRNA Modifications

• Published in: Microorganisms (Basel) Vol. 11; no. 2; p. 355
• Main Authors: Lampi, Mirka, Gregorova, Pavlina, Qasim, M Suleman, Ahlblad, Niklas C V, Sarin, L Peter
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 31.01.2023; MDPI
• Subjects: Adsorption; Anticodons; Bacteria; Genomes; HIV; host–pathogen interaction; Human immunodeficiency virus; Immune response; Infections; Machinery; Parasites; Phages; Polyethylene glycol; Post-transcription; post-transcriptional nucleoside modification; Queuosine; Regulatory mechanisms (biology); Shewanella; Shewanella glacialimarina; Shewanella phage 1/4; Transfer RNA; Translation; tRNA; tRNA Ala; Viruses; translation; Shewanella glacialimarina; Shewanella phage 1/4; transfer RNA; post-transcriptional nucleoside modification; host–pathogen interaction
• ISSN: 2076-2607; 2076-2607
• DOI: 10.3390/microorganisms11020355

Viruses are obligate intracellular parasites that, throughout evolution, have adapted numerous strategies to control the translation machinery, including the modulation of post-transcriptional modifications (PTMs) on transfer RNA (tRNA). PTMs are critical translation regulators used to further host immune responses as well as the expression of viral proteins. Yet, we lack critical insight into the temporal dynamics of infection-induced changes to the tRNA modification landscape (i.e., 'modificome'). In this study, we provide the first comprehensive quantitative characterization of the tRNA modificome in the marine bacterium during Shewanella phage 1/4 infection. Specifically, we show that PTMs can be grouped into distinct categories based on modification level changes at various infection stages. Furthermore, we observe a preference for the UAC codon in viral transcripts expressed at the late stage of infection, which coincides with an increase in queuosine modification. Queuosine appears exclusively on tRNAs with GUN anticodons, suggesting a correlation between phage codon usage and PTM modification. Importantly, this work provides the basis for further studies into RNA-based regulatory mechanisms employed by bacteriophages to control the prokaryotic translation machinery.