PANTŮČEK, Roman, Eva ORÁČOVÁ, Veronika KVARDOVÁ, Vladislava RŮŽIČKOVÁ, Petr PETRÁŠ and Jiří DOŠKAŘ. Multiplex PCR for detection of Staphylococcus aureus prophages. In 10th International Symposium on Staphylococci and Staphylococcal Infections. Tsukuba, Japan: Juntendo University, 2002, p. 66.
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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
Original language English
Type of outcome Proceedings paper
Field of Study Genetics and molecular biology
Country of publisher Japan
Confidentiality degree is not subject to a state or trade secret
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 Bacterial Typing Techniques, bacteriophages, DNA, Lysogeny, Multiplex PCR, Prophage detection, Staphylococcus aureus
Tags International impact, Reviewed
Changed by Changed by: prof. RNDr. Roman Pantůček, Ph.D., učo 842. Changed: 31/10/2008 15:02.
Abstract
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 projectName: Molekulární diagnostika, epidemiologie a klasifikace klinicky významných grampozitivních koků
Investor: Czech Science Foundation, Molecular diagnostic, epidemiology and classification of pathogenic Gram positive cocci
MSM 143100008, plan (intention)Name: Genomy a jejich funkce
Investor: Ministry of Education, Youth and Sports of the CR, Genomes and their functions
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