KUNTOVÁ, Lucie, Ivana MAŠLAŇOVÁ, Radka OBOŘILOVÁ, Hana ŠIMEČKOVÁ, Adéla FINSTRLOVÁ, Pavol BÁRDY, Tibor BOTKA, Zdeněk FARKA, Jiří DOŠKAŘ and Roman PANTŮČEK. Rather die than be taken by the phage: Staphylococcus aureus prophage immunity protein protects population against kayviruses. In NIVB Meeting 2022. 2022. ISSN 2336-7210.
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Basic information
Original name Rather die than be taken by the phage: Staphylococcus aureus prophage immunity protein protects population against kayviruses
Authors KUNTOVÁ, Lucie, Ivana MAŠLAŇOVÁ, Radka OBOŘILOVÁ, Hana ŠIMEČKOVÁ, Adéla FINSTRLOVÁ, Pavol BÁRDY, Tibor BOTKA, Zdeněk FARKA, Jiří DOŠKAŘ and Roman PANTŮČEK.
Edition NIVB Meeting 2022, 2022.
Other information
Original language English
Type of outcome Konferenční abstrakta
Country of publisher Czech Republic
Confidentiality degree is not subject to a state or trade secret
WWW URL
Organization Přírodovědecká fakulta – Repository – Repository
ISSN 2336-7210
Keywords in English non-traditional antibacterials; phage therapy; bacteriophage; phage resistance; cell death; abortive infection
Links LX22NPO5103, research and development project.
Changed by Changed by: RNDr. Daniel Jakubík, učo 139797. Changed: 14/3/2023 03:37.
Abstract
Bacteriophages are crucial in shaping population of pathogens, such as Staphylococcus aureus. Prophages play an important role in the virulence, pathogenesis or host preference, as well as in horizontal gene transfer. On the other hand, broad host range staphylococcal bacteriophages of the genus Kayvirus are promising agents for therapeutic applications. The lysogens become immune to infection by closely related phages, but the interactions between temperate and lytic staphylococcal phages are not understood. We describe a resistance mechanism towards lytic phages of the genus Kayvirus, mediated by S. aureus prophage accessory gene. The responsible membrane-anchored protein shows the presence of a putative membrane-binding α-helix in its N-terminal part and a cytoplasmic positively charged C-terminus. We demonstrated that the mechanism of action does not prevent the infecting Kayvirus to adsorb onto the host cell, deliver its genome into the cell but, phage replication is halted. Changes in the cell membrane polarity and permeability, which lead to prophage-activated cell death were observed from 10 min after the infection. Furthermore, we describe a mechanism of overcoming resistance in a spontaneous host-range Kayvirus mutant in which a gene fusion has emerged, and which was selected on S. aureus strain harbouring a prophage encoding the immunity protein.
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  • a concrete person Mgr. Lucie Vařechová, uco 106253
  • a concrete person RNDr. Daniel Jakubík, uco 139797
  • a concrete person Mgr. Jolana Surýnková, uco 220973
  • a concrete person Mgr. Michal Maňas, uco 2481
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