a 2022

Rather die than be taken by the phage: Staphylococcus aureus prophage immunity protein protects population against kayviruses

KUNTOVÁ, Lucie, Ivana MAŠLAŇOVÁ, Radka OBOŘILOVÁ, Hana ŠIMEČKOVÁ, Adéla FINSTRLOVÁ et. al.

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

Language

English

Type of outcome

Konferenční abstrakta

Country of publisher

Czech Republic

Confidentiality degree

is not subject to a state or trade secret

References:

Organization

Přírodovědecká fakulta – Repository – Repository

ISSN

Keywords in English

non-traditional antibacterials; phage therapy; bacteriophage; phage resistance; cell death; abortive infection

Links

LX22NPO5103, research and development project.
Changed: 14/3/2023 03:37, RNDr. Daniel Jakubík

Abstract

V originále

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.

Files attached