Detailed Information on Publication Record
2002
Multiplex PCR for detection of Staphylococcus aureus prophages
PANTŮČEK, Roman, Eva ORÁČOVÁ, Veronika KVARDOVÁ, Vladislava RŮŽIČKOVÁ, Petr PETRÁŠ et. al.Basic information
Original name
Multiplex PCR for detection of Staphylococcus aureus prophages
Authors
PANTŮČEK, Roman (203 Czech Republic, guarantor), Eva ORÁČOVÁ (203 Czech Republic), Veronika KVARDOVÁ (203 Czech Republic), Vladislava RŮŽIČKOVÁ (203 Czech Republic), Petr PETRÁŠ (203 Czech Republic) and Jiří DOŠKAŘ (203 Czech Republic)
Edition
Tsukuba, Japan, 10th International Symposium on Staphylococci and Staphylococcal Infections, p. 66-66, 2002
Publisher
Juntendo University
Other information
Language
English
Type of outcome
Stať ve sborníku
Field of Study
Genetics and molecular biology
Country of publisher
Japan
Confidentiality degree
není předmětem státního či obchodního tajemství
RIV identification code
RIV/00216224:14310/02:00006633
Organization unit
Faculty of Science
Keywords in English
Bacterial Typing Techniques; DNA; Bacteriophages; Staphylococcus aureus; Lysogeny; Multiplex PCR; Prophage detection
Tags
Tags
International impact, Reviewed
Změněno: 31/10/2008 15:02, prof. RNDr. Roman Pantůček, Ph.D.
Abstract
V originále
Background.Bacteriophages play an important part in gene transfer and gene expression in S.aureus strains and thus also in their virulence and antibiotic resistance.A set of primers for multiplex PCR was designed for identification of prophages of serogroups A,B,F and L in lysogenic and polylysogenic S.aureus strains. Methods.In the genomes of International Typing Set bacteriophages,the sequences specific for both the phage species and serogroups A (ö 3A),B (ö 53),F (ö 77)and L (ö 187)were estimated.The designed primers amplify specific genomic sequences of sizes characteristic of each of the phage species. The multiplex PCR specificity was verified on DNAs of 26 bacteriophages,9 lysogenized and 2 prophageless S.aureus strains. Results.One to three prophages of different serogroups were identified unambiguously in each of 40 clinical strains including 25 MRSA strains.Detectability of prophages by multiplex PCR is comparable with that by phage-specific probes prepared in our laboratory (Doskar et al.,2000,Can.J.Microbiol.46:1066-1076). Conclusions.In view of significant differences in the prophage content between S.aureus closely related isolates,prophage profiling is recommended as a highly sensitive method for strain discrimination.
Links
GA301/02/1505, research and development project |
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MSM 143100008, plan (intention) |
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