HOLOCHOVÁ, Pavla, Vladislava RŮŽIČKOVÁ, Roman PANTŮČEK and Jiří DOŠKAŘ. Genome analysis of staphylococcal exfoliative toxin A converting bacteriophages. In XII. Setkání biochemiků a molekulárních biologů. Sborník příspěvků. Brno: Masarykova univerzita, 2008, p. 33. ISBN 978-80-210-4526-2.
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Basic information
Original name Genome analysis of staphylococcal exfoliative toxin A converting bacteriophages
Name in Czech Analýza genomu exfoliatin A konvertujících stafylokokových bakteriofágů
Authors HOLOCHOVÁ, Pavla (203 Czech Republic), Vladislava RŮŽIČKOVÁ (203 Czech Republic, guarantor), Roman PANTŮČEK (203 Czech Republic) and Jiří DOŠKAŘ (203 Czech Republic).
Edition Sborník příspěvků. Brno, XII. Setkání biochemiků a molekulárních biologů, p. 33-33, 2008.
Publisher Masarykova univerzita
Other information
Original language English
Type of outcome Proceedings paper
Field of Study Genetics and molecular biology
Country of publisher Czech Republic
Confidentiality degree is not subject to a state or trade secret
WWW URL
RIV identification code RIV/00216224:14310/08:00025766
Organization unit Faculty of Science
ISBN 978-80-210-4526-2
Keywords in English Staphylococcus aureus; exfoliative toxin A; converting phage
Tags converting phage, exfoliative toxin A, Staphylococcus aureus
Tags International impact
Changed by Changed by: prof. RNDr. Roman Pantůček, Ph.D., učo 842. Changed: 11/6/2010 09:27.
Abstract
Introduction: The exfoliative toxin A (ETA) is coded by the eta gene of S. aureus prophage. We isolated three eta-positive phages from the clinical S. aureus strains. ETA-negative strain SAU1039 was lysogenized by these phages and was converted into a producer of ETA. Our results indicate that ETA-converting B phages that morphologically resemble the phages of the family Siphoviridae seem to be the major mediators of the eta gene horizontal transfer among the S. aureus strains. We also found that the eta-positive A phage transposed the eta gene into recipient strain, but the lysogens were not able to produce the ETA. On the basis of genomic sequence analysis and alignments both the converting B phages were found to be equal but they differed from the eta-positive A phage in some characteristics. Methods: PCR detection of integrase types and DNA regions: integrase (int), terminase (ter), portal protein (por), holin (hol) amidase (ami), and exfoliative toxin A (eta) genes. Sequencing of target genes, genomic regions or two conservative segments (H3 and H4).Comparative genomics of A and B phages based on sequence studies. Comparison with known sequences of Staphylococcus phages accessible from bioinformatics sources. Results: We carried out the molecular analysis of three ETA-converting phages, i.e. serotype A like phi435 and two serotype B like phages designated phi531 and phi557. We focused our attention on the int, ter, por, hol, ami and eta genes, and two conservative segments H3 and H4 located on two HindIII restriction fragments. On the basis of analyses of target sequences we found out the high sequence similarity between the eta-positive B phages from our region and the Japanese phage phiETA (GenBank acc. no. AP001553). The A phage showed the gene sequence similarities with B phages but differed from them in two genomic regions, the por gene and H4 segment. Conclusions: We found the high sequence similarity in studied genome regions between our ETA-converting B phages and the reference ETA-converting phage phiETA (GenBank acc. no. AP001553) but they showed some genomic differences from the eta-positive A phage. The manner how the A phage has acquired the eta gene remains to be elucidated.
Abstract (in Czech)
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MSM0021622415, plan (intention)Name: Molekulární podstata buněčných a tkáňových regulací
Investor: Ministry of Education, Youth and Sports of the CR, Molecular basis of cell and tissue regulations
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