a 2016

Complete genomes of ETA-converting bacteriophages isolated from impetigo strains of Staphylococcus aureus

BOTKA, Tibor; Vladislava RŮŽIČKOVÁ; Hana KONEČNÁ; Roman PANTŮČEK; Ivan RYCHLÍK et al.

Základní údaje

Originální název

Complete genomes of ETA-converting bacteriophages isolated from impetigo strains of Staphylococcus aureus

Vydání

Viruses of Microbes 2016 - EMBO Conference Series, Liverpool, United Kingdom, 2016

Další údaje

Jazyk

angličtina

Typ výsledku

Konferenční abstrakt

Obor

Genetika a molekulární biologie

Stát vydavatele

Velká Británie a Severní Irsko

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Označené pro přenos do RIV

Ne

Organizační jednotka

Přírodovědecká fakulta

Klíčová slova anglicky

Staphylococcus; bacteriophage; Exfoliative toxin A; structure proteins; genome analysis,

Příznaky

Mezinárodní význam, Recenzováno
Změněno: 25. 7. 2016 10:23, Mgr. Tibor Botka, Ph.D.

Anotace

V originále

Exfoliative toxin A (ETA)-coding temperate bacteriophages are the main contributors to the toxic phenotype of impetigo strains of Staphylococcus aureus. Two eta gene-positive phages were isolated from S. aureus strains which were implicated in massive outbreaks of neonatal vesiculate infections in several Czech maternity hospitals. Phages designated phiB166 and phiB236 were characterized in detail to elucidate their genome diversity. Both the phages were able to incorporate their genomes into the chromosome of a prophageless S. aureus strain which afterwards converted into an exfoliative toxin A producer. Complete phage genome sequences were determined and annotated. Besides identification of all coding ORFs, promoters and intrinsic terminators were predicted. With respect to the functional genomic architecture, the genomes were divided into five regions. The comparative analysis revealed major variances between the phages. They differed in the genome size, number of open reading frames (ORFs) and genome architecture. Many non-homologous and unique sequences located in the genomes were identified. High mutual sequence similarity was detected only in the terminal region. In addition, proteomic analysis, based on the SDS-PAGE, showed major differences between capsid compounds. Conclusive sequence analyses revealed that phiB166 and phiB236 are not closely related to each other or to other previously reported eta or non eta phages. Sequences gained by possible recombination were identified in genomes of both phages. Thus, these phages represent the recent new lineages of as yet undescribed ETA-converting bacteriophages. Their genomic mosaicism reveals them as a fluid gene pool to confer new properties to co-replicating phages and also as mediators of the S. aureus pathogenicity.

Návaznosti

ED1.1.00/02.0068, projekt VaV
Název: CEITEC - central european institute of technology
GBP206/12/G151, projekt VaV
Název: Centrum nových přístupů k bioanalýze a molekulární diagnostice
NT12395, projekt VaV
Název: Molekulární průkaz a analýza invazivních kmenů small colony variants (SCV) a rezistentních kmenů S. aureus od pacientů s cystickou fibrózou