- PII
- 10.31857/S0026365624030144-1
- DOI
- 10.31857/S0026365624030144
- Publication type
- Status
- Published
- Authors
- Volume/ Edition
- Volume 93 / Issue number 3
- Pages
- 362-367
- Abstract
- Recently acquired data suggest that many infections are associated with formation of multispecies biofilms, in which both antibiotic sensitivity and the permeability of the extracellular matrix differ from those of monocultures. In this work, we show that addition of cell-free culture liquid of Staphylococcus aureus to the biofilms of Klebsiella pneumoniae and Pseudomonas aeruginosa increased the content of α- and β-polysaccharides in the matrix up to twofold, which in turn probably affected the biofilm structure. Increased content of the polysaccharide component was also confirmed by a significantly increased expression of the K. pneumoniae pgaA gene and of the P. aeruginosa pelA and pslA genes in the presence of S. aureus culture liquid.
- Keywords
- бактериальные биопленки Staphylococcus aureus Klebsiella pneumoniae Pseudomonas aeruginosa внеклеточный матрикс биохимический состав экспрессия генов
- Date of publication
- 15.05.2024
- Year of publication
- 2024
- Number of purchasers
- 0
- Views
- 34
References
- 1. Baidamshina D., Trizna E., Holyavka M. Targeting microbial biofilms using Ficin, a nonspecific plant protease // Sci. Rep. 2017. V. 7. Art. 46068.
- 2. Bogachev M., Volkov V., Markelov O., Trizna E., Baydamshina D., Melnikov V., Zelenikhin P., Murtazina R., Sharafutdinov I., Kayumov A. Fast and simple tool for the quantification of biofilm-embedded cells sub-populations from fluorescent microscopic images // PLoS One. 2018. V. 13. Art. e0193267.
- 3. Bottery M. J., Pitchford J. W., Friman V. P. Ecology and evolution of antimicrobial resistance in bacterial communities // ISME J. 2021. V. 15. P. 939‒948.
- 4. Chen K. M., Chiang M. K., Wang M., Ho H. C., Lu M. C., Lai Y. C. The role of pgaC in Klebsiella pneumoniae virulence and biofilm formation // Microb. Pathog. 2014. V. 10. P. 89‒99.
- 5. Chew S. C., Kundukad B., Seviour T., Van der Maarel J. R.C., Yang L., Rice S. A., Doyle P., Kjelleberg S. Dynamic remodeling of microbial biofilms by functionally distinct exopolysaccharides // mBio. 2014. V. 5. Art. e01536–14.
- 6. Ciofu O., Moser C., Jensen P. Ø., Høiby N. Tolerance and resistance of microbial biofilms // Nature Rev. Microbiol. 2022. V. 20. P. 621‒635.
- 7. Colvin K. M., Gordon V. D., Murakami K., Borlee B. R., Wozniak D. J., Wong G. C. L. The pel polysaccharide can serve a structural and protective role in the biofilm matrix of Pseudomonas aeruginosa // PLoS Pathog. 2011. V. 7. Art. e1001264.
- 8. Dalton T., Dowd S. E., Wolcott R. D., Sun Y., Watters C., Griswold J. A., Rumbaugh K. P. An in vivo polymicrobial biofilm wound infection model to study interspecies interactions // PLoS One. 2011. V. 6. Art. e27317.
- 9. Eick S. Biofilms. Oral Biofilms, 2020. 232 p. https://doi.org/10.1159/000510184
- 10. Fedorova M. S., Mironova A. V., Kayumov A. R. Cell-free supernatant of Staphylococcus aureus culture increases antimicrobials susceptibility of Pseudomonas aeruginosa // Opera Medica et Physiologica. 2022. V. 9. P. 113‒120.
- 11. Hobley L., Harkins C., MacPhee C., Stanley-Wall N. R. Giving structure to the biofilm matrix: an overview of individual strategies and emerging common themes // FEMS Microbiol. Revs. 2015. V. 39. P. 649‒669.
- 12. Itoh Y., Rice J. D., Goller C., Pannuri A., Taylor J., Meisner J., Beveridge T. J., Preston J. F., Romeo T. Roles of pgaABCD genes in synthesis, modification, and export of the Escherichia coli biofilm adhesin poly-β-1,6-N-acetyl-D-glucosamine // J. Bacteriol. 2008. V. 190. P. 3670‒3680.
- 13. Kayumov A., Khakimullina E., Sharafutdinov I., Trizna E., Latypova L., Lien H., Margulis A., Bogachev M., Kurbangalieva A. Inhibition of biofilm formation in Bacillus subtilis by new halogenated furanones // J. Antibiot. (Tokyo). 2015. V. 68. P. 297‒301.
- 14. Kot B., Sytykiewicz H., Sprawka I. Expression of the biofilm-associated genes in methicillin-resistant Staphylococcus aureus in biofilm and planktonic conditions // Int. J. Mol. Sci. 2018. V. 19. Art. 3487.
- 15. Kranjec C., Morales Angeles D., Torrissen Mårli M., Fernández L., García P., Kjos M., Diep D. B. Staphylococcal biofilms: Challenges and novel therapeutic perspectives // Antibiotics. 2021. V. 10. Art. 131.
- 16. Mironova A. V., Karimova A. V., Bogachev M. I., Kayumov A. R., Trizna E. Y. Alterations in antibiotic susceptibility of Staphylococcus aureus and Klebsiella pneumoniae in dual species biofilms // Int. J. Mol. Sci. 2023. V. 24. Art. 8475.
- 17. Orazi G., O’Toole G.A. “It takes a village”: mechanisms underlying antimicrobial recalcitrance of polymicrobial biofilms // J. Bacteriol. 2019. V. 202. Art. e00530–19.
- 18. Otto M. Staphylococcal biofilms // Microbiol. Spectr. 2018. V. 6. P. 1–26. https://doi.org/10.1128/microbiolspec.GPP3-0023-2018
- 19. Radlinski L. C., Rowe S. E., Brzozowski R., Wilkinson A. D., Huang R., Eswara P., Conlon B. P. Chemical induction of aminoglycoside uptake overcomes antibiotic tolerance and resistance in Staphylococcus aureus // Cell. Chem. Biol. 2019. V. 26. P. 1355‒1364.
- 20. Ryder C., Byrd M., Wozniak D. J. Role of polysaccharides in Pseudomonas aeruginosa biofilm development // Curr. Opin. Microbiol. 2007. V. 10. P. 644‒648.
- 21. Sambrook J., Fritsch E. F., Maniatis T. Molecular cloning: a laboratory manual. Cold Spring Habor Laboratory press, 1989.
- 22. Sharma D., Misba L., Khan A. U. Antibiotics versus biofilm: an emerging battleground in microbial communities // Antimicrob. Resist. Infect. Control. 2019. V. 8. P. 1‒10. https://doi.org/10.1186/s13756-019-0533-3
- 23. Trizna E. Y., Yarullina M. N., Baidamshina D. R., Mironova A. V., Akhatova F. S., Rozhina E., Fakhrullin R. F., Khabibrakhmanova A. M., Kurbangalieva A. R., Bogachev M. I., Kayumo, A. R. Bidirectional alterations in antibiotics susceptibility in Staphylococcus aureus‒Pseudomonas aeruginosa dual-species biofilm // Sci. Rep. 2018. V. 10. Art. 14849.