Inhibitory effects of polysorbate 80 on MRSA biofilm formed on different substrates including dermal tissue

Yutaka Ueda1, Kota Mashima1, Motoyasu Miyazaki2

  • 1Department of Pharmacy, Fukuoka University Hospital, Fukuoka, Japan.

Scientific Reports
|March 1, 2019
PubMed

Insights

Polysorbate 80 (PS80) effectively prevents methicillin-resistant Staphylococcus aureus (MRSA) biofilms by inhibiting bacterial adhesion, not disrupting existing biofilms. This surfactant shows low cytotoxicity, making it suitable for wound care and medical devices.

Area of Science:

  • Microbiology
  • Biomaterials Science
  • Medical Chemistry

Background:

  • Methicillin-resistant Staphylococcus aureus (MRSA) forms persistent biofilms on necrotic tissues and medical devices.
  • Surfactants are known to affect biofilms, but their mechanisms and clinical applicability require further investigation.
  • Minimizing cytotoxicity is crucial for clinical use of surfactants in treating MRSA infections.

Purpose of the Study:

  • To investigate the inhibitory effects of four surfactants on MRSA biofilm formation.
  • To identify the most suitable surfactant with minimal cytotoxicity for clinical applications.
  • To elucidate the mechanism of action and substrate-dependency of effective surfactants.

Main Methods:

  • Screening of four different surfactants for their impact on MRSA biofilm formation.
  • Assessment of bacterial adhesion inhibition versus biofilm disruption.
  • Evaluation of cytotoxicity of effective surfactants on 3T3 fibroblasts.
  • Testing the substrate-dependent efficacy of surfactants on plastic, silicon, dermal tissues, and stainless-steel.

Main Results:

  • Polysorbate 80 (PS80), a nonionic surfactant, demonstrated the most significant MRSA biofilm inhibitory effect.
  • PS80 inhibited bacterial adhesion to substrates rather than disrupting pre-formed biofilms.
  • The effective concentration of PS80 exhibited low cytotoxicity towards 3T3 fibroblasts.
  • PS80's efficacy was substrate-dependent, showing positive effects on plastic, silicon, and dermal tissues, but not on stainless-steel.

Conclusions:

  • PS80 is effective in preventing MRSA biofilm formation on various substrates, including tissues and foreign bodies.
  • The mechanism involves inhibition of bacterial adhesion, with minimal cytotoxicity.
  • PS80 holds potential for clinical use as a wound washing solution or for pretreatment of indwelling catheters to prevent MRSA biofilms.

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