Affiliations 

  • 1 Faculty of Science, University of Nottingham Malaysia Campus, Jalan Broga, Semenyih, Selangor 43500, Malaysia. Carolina.Santiago@nottingham.edu.my
  • 2 Faculty of Science, University of Nottingham Malaysia Campus, Jalan Broga, Semenyih, Selangor 43500, Malaysia. kuanhon.lim@nottingham.edu.my
  • 3 Faculty of Science, University of Nottingham Malaysia Campus, Jalan Broga, Semenyih, Selangor 43500, Malaysia. Sandy.Loh@nottingham.edu.my
  • 4 Faculty of Science, University of Nottingham Malaysia Campus, Jalan Broga, Semenyih, Selangor 43500, Malaysia. Kang-Nee.Ting@nottingham.edu.my
Molecules, 2015 Mar 10;20(3):4473-82.
PMID: 25764489 DOI: 10.3390/molecules20034473

Abstract

Formation of biofilms is a major factor for nosocomial infections associated with methicillin-resistance Staphylococcus aureus (MRSA). This study was carried out to determine the ability of a fraction, F-10, derived from the plant Duabanga grandiflora to inhibit MRSA biofilm formation. Inhibition of biofilm production and microtiter attachment assays were employed to study the anti-biofilm activity of F-10, while latex agglutination test was performed to study the influence of F-10 on penicillin-binding protein 2a (PBP2a) level in MRSA biofilm. PBP2a is a protein that confers resistance to beta-lactam antibiotics. The results showed that, F-10 at minimum inhibitory concentration (MIC, 0.75 mg/mL) inhibited biofilm production by 66.10%; inhibited cell-surface attachment by more than 95%; and a reduced PBP2a level in the MRSA biofilm was observed. Although ampicilin was more effective in inhibiting biofilm production (MIC of 0.05 mg/mL, 84.49%) compared to F-10, the antibiotic was less effective in preventing cell-surface attachment. A higher level of PBP2a was detected in ampicillin-treated MRSA showing the development of further resistance in these colonies. This study has shown that F-10 possesses anti-biofilm activity, which can be attributed to its ability to reduce cell-surface attachment and attenuate the level of PBP2a that we postulated to play a crucial role in mediating biofilm formation.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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