Virion content unpacked by long-read sequencing: Stress-induced changes in transmitted staphylococcal mobilome due to phage-satellite interactions

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Publikace nespadá pod Ústav výpočetní techniky, ale pod Přírodovědeckou fakultu. Oficiální stránka publikace je na webu muni.cz.
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BOTKA Tibor SMETANOVÁ Soňa VINCO Adam KUČEROVÁ Eliška ROVŇÁKOVÁ Kristína SIVÁKOVÁ Alena MAŠLAŇOVÁ Ivana PANTŮČEK Roman

Rok publikování 2025
Druh Článek v odborném periodiku
Časopis / Zdroj NUCLEIC ACIDS RESEARCH
Fakulta / Pracoviště MU

Přírodovědecká fakulta

Citace
www https://doi.org/10.1093/nar/gkaf1165
Doi https://doi.org/10.1093/nar/gkaf1165
Klíčová slova Mobile Genetic Elements; Nanopore Sequencing; Horizontal Gene Transfer; Phage Therapy; DNA packaging; Bacteriophage Satellites
Přiložené soubory
Popis The evolution of the virulence and antibiotic resistance of staphylococci, important opportunistic pathogens, is strongly determined by their mobilome, which can spread by phage virions or small-headed particles resulting from the hijacking of helper phage machinery by phage satellites named phage-inducible chromosomal islands (PICIs). Despite known mechanisms of the formation of transducing particles, it has not yet been possible to analyze their DNA content at the single-virion level. Using the Staphylococcus epidermidis model and long-read nanopore sequencing, we determined the sequence structure and ratio of phage and PICI genophores, plasmid, and bacterial DNA packaged in normal and small-headed virions. It was shown that the ratios vary mainly depending on the helper phage and the antimicrobial used for induction. When the effect of a strictly lytic phage and its combination with ciprofloxacin on a packaged mobilome was analyzed, no significant increase in mobilome dissemination was observed compared to antibiotics alone. Here, we demonstrate a novel approach for the analysis of transduced bacterial mobilome and show in vitro that lytic phage-based therapeutic strategies do not increase the risk of mobile genetic element transfer.
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