Vorobey E. S., Voronkova O. S., Vinnikov A. I.

AN INFLUENCE OF STAPHYLOCOCCAL BACTERIOPHAGE ON BIOFILM OF STAPHYLOCOCCUS AUREUS STRAINS SENSITIVE AND RESISTANT TO CEFOTAXIME AND AZITHROMYCIN, DEPENDING ON CHEMICAL COMPOSITION OF MATRIX


About the author:

Vorobey E. S., Voronkova O. S., Vinnikov A. I.

Heading:

MICROBIOLOGY

Type of article:

Scentific article

Annotation:

Removal of mature biofilms is the main task of therapy, because biofilms are the basement of the pathogenic process. The ability of active matrix to bind antibiotics or reduce the diffusion through the biofilm leads to incomplete removal of microorganisms, which attend to their survival and formation of chronic processes. An influence on staphylococcal biofilms can be done by destruction of extracellular polysaccharide matrix. This treatment, which may influence on the structure of the biofilm, is more effective than standard antibiotic therapy. It was established that the phage progeny spread radially through the biofilm, infecting neighboring cells and destroying the biofilm matrix. For this purposes phages producing the depolimerase, which may destroy biofilms matrix that is significantly depends on the structure of the polymer matrix. It was showed that the effect of the drug «Bacteriophage staphylococcal liquid» on 72-hour biofilms of investigated strains, sensitive to cefotaxime and azithromycin, characterized by decreasing of absorbance level of eluted dye on 19.1%, while the number of cells in the biofilm decreased in 253.0 times. More significant effect of staphylococcal bacteriophage was determined for biofilms of strains, resistant to cefotaxime and azithromycin. This effect characterized as a decrease of optical density on 33.9%, while the number of cells decreased in 393.6 times. An important step of our research was to study the biochemical composition of the polymer matrix of staphylococcal biofilms. Study the composition of biofilms matrix based on the specific destruction of it components. The percent of exopolysaccharides in the composition of biofilms matrix, formed by 72-hour, was determine by treatment of sodium periodate. It was found that after treatment the decreasing of optical density of eluted dye at 47.00 ± 2.87% for antibiotic sensitive strain and 59.02 ± 2.10% — for resistant took place. The presence of proteins was determine by using of proteinase K and trypsin. After treatment of the 72-hour biofilm by proteinase K absorbance of eluted dye, delayed by biofilm, decreased on 8.52 ± 1.72% compare to 72-hour control biofilm without enzyme adding for sensitive to antibiotic strain and on 3.52 ± 1.11% — for resistant strain. After trypsin adding decrease of absorbance of eluted dye was less — 12.16 ± 1.49% for sensitive to antibiotic strain and 7.20 ± 2.12% — for resistant. The content of the extracellular matrix DNA was determined with use of DNAase. The decrease of biofilms absorbance on 15.72 ± 2.55% compare to control biofilm for strain sensitive to antibiotic and 14.50 ± 1.33% — for resistant. This indicate that the main component of the biofilm matrix of studied strains are exopolysaccharides, and their number are on 12.02% higher in the antibioticresistant strain. The results demonstrate the effectiveness of the phages drugs use to control the growth of biofilms formed by Staphylococcus aureus strains, the matrix of that consisting of a large number of exopolysaccharide. For inhibition of the biofilmformation the study of the relation of matrix structure and sensitivity to antibiotics is necessary and the search of therapeutic drugs capable to inhibit the production of exopolysaccharides is main task of microbiology.

Tags:

staphylococci, biofilm, matrix, exopolysaccharides, polysacchariddepolimerase

Bibliography:

  • 1. Биопленки патогенных бактерий и их роль в хронизации инфекционного процесса. Поиск средств борьбы с биопленками / Ю. М. Романова, Л. В. Диденко, Э. Р. Толордава [и др.] // Вестник РАМН. – 2011. – № 10. – С. 31-39.
  • 2. Современные технологии исследования бактериальных биопленок / И. В. Чеботарь, А. Г. Погорелов, В. А. Яшин [и др.] // Современные технологии в медицине. – 2013. – Т. 5, № 1. – С. 14-20.
  • 3. Abedon S. T. Ecology of anti-biofilm agents II: bacteriophage exploitation and biocontrol of biofilm bacteria / S. T. Abedon // Pharmaceuticals. – 2015. – Vol. 8, № 3. – P. 559-589.
  • 4. Adams M. H. An enzyme produced by a phage-host cell system II. The properties of the polysaccharide depolymerase / M. H. Adams, B. H. Park // Virology. – 1956. – Vol. 2, № 6. – P. 719-736.
  • 5. Bacterial extracellular polysaccharides involved in biofilm formation / B. Vu, M. Chen, R. J. Crawford [et al.] // Molecules. – 2009. – Vol. 14, № 7. – P. 2535-2554.
  • 6. Bacteriophage and associated polysaccharide depolymerases – novel tools for study of bacterial biofilms / K. A. Hughes, I. W. Sutherland, J. Clark [et al.] // Journal of Applied Microbiology. – 1998. – Vol. 85, № 3. – P. 583-590.
  • 7. Chan B. K. Bacteriophages and their enzymes in biofilm control / B. K. Chan, S. T. Abedon // Current Pharmaceutical Design. – 2015. – Vol. 21, № 1. – P. 85-99.
  • 8. Differential roles of Poly-N-acetylglucosamine surface polysaccharide and extracellular DNA in Staphylococcus aureus and Staphylococcus epidermidis biofilms / E. A. Izano, M. A. Amarante, W. B. Kher [et al.] // Applied and Environmental Microbiology. – 2008. – Vol. 74, № 2. – P. 470-476.
  • 9. Doolittle M. M. Tracing the interaction of bacteriophage with bacterial biofilms using fluorescent and chromogenic probes / M. M. Doolittle, J. J. Cooney, D. E. Caldwell // Journal of Industrial Microbiology. – 1996. – Vol. 16. – P. 331-341.
  • 10. Extracellular DNA in biofilms / L. Montanaro, A. Poggi, L. Visai [et al.] // The International Journal of Artificial Organs. – 2011. – Vol. 34, № 9. – P. 824-831.
  • 11. Flemming H.-C. The biofilm matrix / H.-C. Flemming, J. Wingender // Nature Reviews Microbiology. – 2010. – Vol. 8, № 9. – P. 623-633.
  • 12. Frank K. L. Poly-N-Acetylglucosamine is not a major component of the extracellular matrix in biofilms formed by icaADBC-positive Staphylococcus lugdunensis isolates / K. L. Frank, R. Patel // Infection and Immunity. – 2007. – Vol. 75, № 10. – P. 4728-4742.
  • 13. How Staphylococcus aureus biofilms develop their characteristic structure / S. Periasamy, H.-S. Joo, A. C. Duong [et al.] // Proceedings of the National Academy of Sciences of the United States of America. – 2012. – Vol. 109, № 4. – P. 1281-1286.
  • 14. Kutateladze M. Bacteriophages as potential new therapeutics to replace or supplement antibiotics / M. Kutateladze, R. Adamia // Trends in Biotechnology. – 2010. –Vol. 28, № 12. – P. 591-595.
  • 15. Lindberg A. A. Bacterial surface carbohydrates and bacteriophage adsorption / A. A. Lindberg // Surface Carbohydrates of the Prokaryotic Cell / ed. I. W. Sutherland. – London: Academic Press, 1977. – P. 289-356.
  • 16. Protein A-mediated multicellular behavior in Staphylococcus aureus / N. Merino, A. Toledo-Arana, M. Vergara-Irigaray [et al.] // Journal of Bacteriology. – 2009. – Vol. 191, № 3. – P. 832-843.
  • 17. Scholl D. Polysaccharide-degrading phages / D. School, C. Merril // Phages: their role in bacterial pathogenesis and biotechnology / eds. M. K. Waldor, D. I. Friedman, S. L. Adhya. – Washington DC: ASM Press, 2005. – P. 400-414.
  • 18. Susceptibility of staphylococcal biofilms to enzymatic treatments depends on their chemical composition / P. Chaignon, I. Sadovskaya, Ch. Ragunah [et al.] // Applied Microbiology and Biotechnology. – 2007. – Vol. 75, № 1. – P. 125-132.
  • 19. The anchorless adhesin Eap (extracellular adherence protein) from Staphylococcus aureus selectively recognizes extracellular matrix aggregates but binds promiscuously to monomeric matrix macromolecules / U. Hansen, M. Hussain, D. Villone [et al.] // Matrix Biology. – 2006. – Vol. 25, № 4. – P. 252-260.
  • 20. The interaction of phage and biofilms / I. W. Sutherland, K. A. Hughes, L. C. Skillman [et al.] // FEMS Microbiology Letters. – 2004. – Vol. 232, № 1. – P. 1-6. – Mode of access: www.fems-microbiology.org.
  • 21. Wall teichoic acids are dispensable for anchoring the PNAG exopolysaccharide to the Staphylococcus aureus cell surface / M. Vergara-Irigaray, T. Maira-Litran, N. Merino [et al.] // Microbiology. – 2008. – № 154, № 3. – P. 865-877.

Publication of the article:

«Bulletin of problems biology and medicine» Issue 1 part 1 (126), 2016 year, 249-253 pages, index UDK 579.61: 616-095