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2017 | 28 |

Tytuł artykułu

Adhesive and hydrophobic properties of Pseudomonas aeruginosa and Pseudomonas cedrina associated with cosmetics

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
The presence of bacteria in the cosmetic production environment is often connected with non-sterile raw materials, inappropriate production lines disinfection or cross contamination. Among bacteria isolated from the environment, opportunistic pathogens can be also found, posing a risk to patients with lowered immunity. Moreover, their susceptibility to antibiotics and disinfectants is frequently decreased as they develop more complex forms - biofilms. As hydrophobicity and adhesive properties play a vital role in the colonization process the aim of this research was to determine hydrophobic, aggregative and adhesive properties of bacteria isolated from the cosmetics.Bacteria used in the research were isolated from the body balm and the cosmetic preservative (three strains of Pseudomonas aeruginosa and four strains of Pseudomonas cedrina) and identified using 16S rRNA gene sequencing. For those strains and also two reference strains (P. aeruginosa ATCC15442 and P. cedrina DSM17516) an aggregation test, hydrophobicity by two different methods (SAT and MATH) and adhesion to polystyrene by crystal violet binding assay were performed. According to the SAT method more than half of the tested strains were strongly hydrophobic. Using MATH test, it was proved that four strains (P. cedrina DSM17516 and three isolates of P. aeruginosa) were strong hydrophobes, however, the rest of the strains expressed moderate hydrophobicity. Moreover, self-aggregation was also observed and for P. aeruginosa CFII was more than 20%. All of the strains were able to adhere to polystyrene after 30 minutes contact, almost all of them (excluding P. cedrina DSM17516) indicated a moderate adhesion already after four hours of incubation. These results indicate that environmental Pseudomonas strains possess strong hydrophobic and adhesive properties, that may results in a colonization of abiotic surfaces.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

28

Opis fizyczny

p.41-46,fig.,ref.

Twórcy

autor
  • Institute of Fermentation Technology and Microbiology, Faculty of Biotechnology and Food Sciences, Lodz University of Technology, Wolczanska 171/173 St, 90-924 Lodz, Poland
  • Institute of Fermentation Technology and Microbiology, Faculty of Biotechnology and Food Sciences, Lodz University of Technology, Wolczanska 171/173 St, 90-924 Lodz, Poland
autor
  • Institute of Fermentation Technology and Microbiology, Faculty of Biotechnology and Food Sciences, Lodz University of Technology, Wolczanska 171/173 St, 90-924 Lodz, Poland

Bibliografia

  • Birteksoz A.R., Tuysuz M. & Otuk G., 2013, Investigation of preservative efficacy and microbiological content of some cosmetics found on the market. Pakistan Journal of Pharmaceutical Sciences 26: 153–157.
  • Briedenstein E.B.M., De la Fuente-Nunez C. & Hancock R.E.W., 2011, Pseudomonas aeruginosa: all roads lead to resistance. Trends in Microbiology 19: 419–426.
  • Campana R., Scesa C., Patrone V., Vittoria E. & Baffone W., 2006, Microbiological study of cosmetics product during their use by consumers: health risk and efficacy of preservative systems. Letters in Applied Microbiology 43: 301–306.
  • Del Re B., Sgorbati B., Miglioli M. & Palenzona D., 2000, Adhesion, autoaggregation and hydrophobicity of 13 strains of Bifidobacterium longum. Letters in Applied Microbiology 31: 438–442.
  • Garbolińska M., 2010, Microbiological control in the cosmetic industry. Świat Przemysłu Kosmetycznego 2: 26–29.
  • Kadam T.A., Rupa L., Balhal D.K., Totewad N.D. & Gyananath G., 2009, Determination of the degree of hydrophobicity – A technique to assess bacterial colonization on leaf surface and root region of lotus plant. Asian Journal of Experimental Sciences 23(1): 135–139.
  • Kręgiel D., Otlewska A. & Antolak H., 2014, Attachment of Asaia bogorensis originating in fruit-flavored water to packaging materials. BioMed Research International. (http://dx.doi.org/10.1155/2014/514190).
  • Kumar S., Stecher G. & Tamura K., 2016, MEGA7: Molecular Evolutionary Genetics Analysis version 7.0 for bigger datasets. Molecular Biology and Evolution 33: 1870–1874.
  • Matusiak D.M., 2014, Zakażenia układu moczowego z udziałem Proteus mirabilis – rola biofilmu i inkrustacji cewnika urologicznego [Urinary tract infections caused by Proteus mirabilis – role of the biofilm and the encrustation of the urological catheter]. Postępy Mikrobiologii 53(2): 173–181.
  • Nwanyanwu C. & Abu G., 2013, Influence of growth media on hydrophobicity of phenol-utilizing bacteria found in petroleum refinery effluent. International Research Journal of Biological Sciences 2: 6–10.
  • Norouzi F., Mansouri S., Moradi M. & Razavi M., 2010, Comparison of cell surface hydrophobicity and biofilm formation among ESBLand non-ESBL-producing Pseudomonas aeruginosa clinical isolates. African Journal of Microbiology Research 4(11): 1143–1147.
  • PN-EN ISO 17516: 2014-11 Cosmetics-Microbiology-Microbiological limits.
  • Rosenberg M., 1984, Bacterial adherence to hydrocarbons: a useful technique for studying cell surface hydrophobicity. FEMS Microbiology Letters 22: 289-295.
  • Saitou N. & Nei M., 1987, The neighbor-joining method: A new method for reconstructing phylogenetic trees. Molecular Biology and Evolution 4: 406–425.
  • Sedlaćkova P., Cefovsky M., Horsakova I. & Voldfich M., 2011, Cell surface characteristic of Asaia bogorensis – spoilage microorganism of bottled water. Czech Journal of Food Sciences 29(4): 457-461.
  • Stepanovic S., Vukovic D., Dakic I., Savic B. & Svabic- Vlahovic M., 2000, A modified microtiter-plate test for quantification of staphylococcal biofilm formation. Journal of Microbiological Methods 40(2): 175–179.
  • Tamura K., Nei M. & Kumar S., 2004, Prospects for inferring very large phylogenies by using the neighborjoining method. Proceedings of the National Academy of Sciences (USA) 101:11030–11035.
  • Tyfa A., Kunicka-Styczyńska A. & Zabielska J., 2015, Evaluation of hydrophobicity of quantitative analysis of biofilm formation by Alicyclobacillus sp. Acta Biochimica Polonica 62(4): 785–790.
  • Xu H., Zou Y., Lee H.-Y. & Ahn J., 2010, Effect of NaCl on the biofilm formation by foodborne pathogens. Journal of Food Science 75(9): 581-585.
  • Wolska K., Pogorzelska S., Fijoł E., Jakubczak A. & Bukowski K., 2002, Influence on growth conditions on cell surface hydrophobicity of Pseudomonas aeruginosa, Medycyna Doświadczalna i Mikrobiologia 54: 61–66.
  • Zabielska J., Kunicka-Styczyńska A., Rajkowska K. & Tyfa A., 2015, Opportunistic Gram-negative rods’ capability of creating biofilm structures on polivynyl chloride and styrene-acronitrile copolymer surfaces. Acta Biochimica Polonica 62(4): 733–737.
  • Zhang Z., Schwartz S., Wagner L. & Miller W., 2000, A greedy algorithm for aligning DNA sequences. Journal of Computational Biology 7: 203–214.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

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