Establishing Host-Virus Link Through Host Metabolism: Viral DNA SIP Validation Using T4 Bacteriophage and E. coli.
Autor: | Ngo VQH; Université Paris-Saclay, INRAE, PROSE, 92761, Antony, France., Sotomski M; Université Paris-Saclay, INRAE, PROSE, 92761, Antony, France., Guenne A; Université Paris-Saclay, INRAE, PROSE, 92761, Antony, France., Mariadassou M; Université Paris-Saclay, INRAE, MaIAGE, 78350, Jouy-en-Josas, France.; BioinfOmics, MIGALE Bioinformatics Facility, Université Paris-Saclay, INRAE, 78350, Jouy-en-Josas, France., Krupovic M; CNRS UMR6047, Archaeal Virology Unit, Institut Pasteur, Université de Paris, 75015, Paris, France., Enault F; Université Clermont Auvergne, CNRS, LMGE, 63000, Clermont-Ferrand, France., Bize A; Université Paris-Saclay, INRAE, PROSE, 92761, Antony, France. ariane.bize@inrae.fr. |
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Jazyk: | angličtina |
Zdroj: | Current microbiology [Curr Microbiol] 2024 Jul 14; Vol. 81 (9), pp. 266. Date of Electronic Publication: 2024 Jul 14. |
DOI: | 10.1007/s00284-024-03774-x |
Abstrakt: | DNA Stable Isotope Probing is emerging as a potent methodology for investigating host-virus interactions, based on the essential reliance of viruses on host organisms for the production of virions. Despite the anticipated link between host isotopic compositions and the generated virions, the application of stable isotope probing to viral DNA has never been evaluated on simple biological models. In this study, we assessed the efficacy of this method on the bacteriophage T4 and its host, Escherichia coli. Through the cultivation of E. coli cells on a 13 C-enriched substrate and subsequent propagation of T4 bacteriophage, we examine the degree of isotopic enrichment in viral DNA. Our investigation reveals a strong correlation between the proportion of 13 C (© 2024. The Author(s).) |
Databáze: | MEDLINE |
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