Další formáty:
BibTeX
LaTeX
RIS
@inproceedings{560097,
author = {Doškař, Jiří and Pantůček, Roman and Růžičková, Vladislava and Kašpárek, Petr and Eyer, Luděk and Konečná, Hana and Zdráhal, Zbyněk and Preisler, Jan},
address = {Charleston, South Carolina, USA},
booktitle = {11th International Symposium on Staphylococci & Staphylococcal Infections. Plenary Summaries & Poster Abstracts},
keywords = {staphylococcus; bacteriophage},
language = {eng},
location = {Charleston, South Carolina, USA},
pages = {201-201},
publisher = {Medical University of South Carolina},
title = {Genomic and proteomic characterization of the polyvalent staphylophage 812},
url = {http://www.isssi.org/},
year = {2004}
}
TY - JOUR
ID - 560097
AU - Doškař, Jiří - Pantůček, Roman - Růžičková, Vladislava - Kašpárek, Petr - Eyer, Luděk - Konečná, Hana - Zdráhal, Zbyněk - Preisler, Jan
PY - 2004
TI - Genomic and proteomic characterization of the polyvalent staphylophage 812
PB - Medical University of South Carolina
CY - Charleston, South Carolina, USA
KW - staphylococcus
KW - bacteriophage
UR - http://www.isssi.org/
N2 - Virulent and polyvalent staphylophage 812, a member of Myoviridae family, exhibits strong lytic activity on a broad host range of Staphylococcus species, thus being a suitable candidate for treatment of staphylococcal infections. Genome of this phage is represented by linear 145 kb dsDNA. Our study was focused on genome and proteome comparison of 812 wild-type phage, its host-range mutants and related phages U16, 131 and SK311 with the aim to explain molecular basis of differences in their host-range. The genomes of phages under study were compared by DNA restriction analysis, and the genomic regions showing differences in individual phages were characterized in details. The proteome analysis included separation of phage protein lysates by 1D SDS-PAGE with subsequent identification of proteins by peptide mapping using MALDI-TOF mass spectrometry. Comparison of the phage genomes revealed several rearrangements of DNA sequences as well as single nucleotide substitutions in different parts of the genomes. Nucleotide insertions and deletions of various size (~1 to 3 kb) were most frequently found in non-coding terminal genomic regions in phages with different host range. We tried to find possible correlations between mutational changes on DNA and proteome composition of the phages. After SDS-PAGE separation of phage virions digests 15 protein bands with the mass ranging from 15 to 80 kDa were identified. Twelve bands were excised for further analysis by in-gel digestion with consecutive MALDI-TOF MS. Three of the proteins designated 812_mtsp (64.4 kDa), 812_mcp (51.2 kDa) and 812_ORF8 (15.9 kDa) were identified by peptide mapping. Two of them were determined as the major capsid protein and the major tail sheath protein, respectively. Both the proteins show high similarity with the corresponding proteins of the staphylococcal polyvalent phages TWORT and K as well as those of Listeria monocytogenes phage A511. SDS-PAGE revealed size differences of the tail sheat proteins in phages 812, SK311 and U16 which substantially differ in their host range. Thus, the structural changes of tail sheat proteins should be considered as a factor influencing the host range of polyvalent staphylophages.
ER -
DOŠKAŘ, Jiří, Roman PANTŮČEK, Vladislava RŮŽIČKOVÁ, Petr KAŠPÁREK, Luděk EYER, Hana KONEČNÁ, Zbyněk ZDRÁHAL a Jan PREISLER. Genomic and proteomic characterization of the polyvalent staphylophage 812. In \textit{11th International Symposium on Staphylococci \&{} Staphylococcal Infections. Plenary Summaries \&{} Poster Abstracts}. Charleston, South Carolina, USA: Medical University of South Carolina, 2004, s.~201.
|
