Detailed Information on Publication Record
2019
Lytic and genomic properties of spontaneous host-range Kayvirus mutants prove their suitability for upgrading phage therapeutics against staphylococci
BOTKA, Tibor, Roman PANTŮČEK, Ivana MAŠLAŇOVÁ, Martin BENEŠÍK, Petr PETRÁŠ et. al.Basic information
Original name
Lytic and genomic properties of spontaneous host-range Kayvirus mutants prove their suitability for upgrading phage therapeutics against staphylococci
Authors
BOTKA, Tibor (203 Czech Republic, belonging to the institution), Roman PANTŮČEK (203 Czech Republic, guarantor, belonging to the institution), Ivana MAŠLAŇOVÁ (203 Czech Republic, belonging to the institution), Martin BENEŠÍK (203 Czech Republic, belonging to the institution), Petr PETRÁŠ (203 Czech Republic), Vladislava RŮŽIČKOVÁ (203 Czech Republic, belonging to the institution), Pavla HAVLÍČKOVÁ (203 Czech Republic, belonging to the institution), Marian VARGA (203 Czech Republic, belonging to the institution), Helena ŽEMLIČKOVÁ (203 Czech Republic), Ivana KOLÁČKOVÁ (203 Czech Republic), Martina FLORIANOVÁ (203 Czech Republic), Vladislav JAKUBŮ (203 Czech Republic), Renata KARPÍŠKOVÁ (203 Czech Republic) and Jiří DOŠKAŘ (203 Czech Republic, belonging to the institution)
Edition
Scientific Reports, London, Nature Publishing Group, 2019, 2045-2322
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10603 Genetics and heredity
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 3.998
RIV identification code
RIV/00216224:14310/19:00107363
Organization unit
Faculty of Science
UT WoS
000462990000017
Keywords in English
Kayvirus; Viral genetics; Phage Therapy; Methicillin-Resistant Staphylococcus aureus; Host Range; Genetic Polymorphisms
Tags
Tags
International impact, Reviewed
Změněno: 6/2/2023 13:06, Mgr. Tibor Botka, Ph.D.
Abstract
V originále
Lytic bacteriophages are valuable therapeutic agents against bacterial infections. There is continual effort to obtain new phages to increase the effectivity of phage preparations against emerging phage-resistant strains. Here we described the genomic diversity of spontaneous host-range mutants of kayvirus 812. Five mutant phages were isolated as rare plaques on phage-resistant Staphylococcus aureus strains. The host range of phage 812-derived mutants was 42% higher than the wild type, determined on a set of 186 methicillin-resistant S. aureus strains representing the globally circulating human and livestock-associated clones. Comparative genomics revealed that single-nucleotide polymorphisms from the parental phage 812 population were fixed in next-step mutants, mostly in genes for tail and baseplate components, and the acquired point mutations led to diverse receptor binding proteins in the phage mutants. Numerous genome changes associated with rearrangements between direct repeat motifs or intron loss were found. Alterations occurred in host-takeover and terminal genomic regions or the endolysin gene of mutants that exhibited the highest lytic activity, which implied various mechanisms of overcoming bacterial resistance. The genomic data revealed that Kayvirus spontaneous mutants are free from undesirable genes and their lytic properties proved their suitability for rapidly updating phage therapeutics.
Links
GA18-13064S, research and development project |
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NV16-29916A, research and development project |
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QJ1510216, research and development project |
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