Murraya koenigii methanolic extract inhibits bacterial growth and biofilm of Staphylococcus aureus and Enterococcus

Shashank Kashyap1, Yashkumar Rathod1, Sumit Biswas2

  • 1ViStA lab, Department of Biological Sciences, BITS-Pilani, KK Birla Goa Campus, Goa, 403726, India.

Scientific Reports
|October 1, 2025
PubMed

Insights

Murraya koenigii leaf extract effectively combats Staphylococcus aureus and Enterococcus faecalis infections by inhibiting growth and disrupting biofilms. This plant-derived compound shows promise as a novel phytotherapeutic agent against antibiotic-resistant bacteria.

Area of Science:

  • Microbiology
  • Pharmacology
  • Natural Products Chemistry

Background:

  • Hospital-acquired infections caused by Staphylococcus aureus and Enterococcus faecalis are major global health concerns.
  • These pathogens' ability to form biofilms contributes to antibiotic resistance and environmental persistence.
  • There is an urgent need for novel therapeutic strategies to combat these resilient infections.

Purpose of the Study:

  • To investigate the in vitro efficacy of Murraya koenigii methanolic leaf extract (MKM) against Staphylococcus aureus and Enterococcus faecalis.
  • To evaluate the extract's impact on bacterial growth, biofilm formation, and membrane integrity.
  • To identify bioactive compounds in MKM and assess their potential therapeutic applications through in silico analyses.

Main Methods:

  • In vitro antimicrobial activity testing, including Minimum Inhibitory Concentration (MIC) determination.
  • Flow cytometry and confocal imaging to assess membrane damage.
  • Scanning electron microscopy (SEM) for biofilm architecture visualization.
  • High-Resolution Liquid Chromatography-Mass Spectrometry (HR-LC/MS) for compound identification and ADME analysis.
  • In silico molecular docking studies against bacterial biofilm-related proteins.

Main Results:

  • MKM extract demonstrated significant inhibition of both S. aureus and E. faecalis growth at their respective MICs.
  • The extract caused substantial membrane damage in treated bacterial cells.
  • MKM extract effectively disrupted biofilm formation and reduced extracellular polymeric substance (EPS) production.
  • SEM confirmed the disruption of biofilm architecture.
  • In silico analyses revealed strong binding affinities of identified compounds with key biofilm proteins (SpA and Esp).

Conclusions:

  • Murraya koenigii methanolic leaf extract possesses significant antimicrobial and anti-biofilm properties against S. aureus and E. faecalis.
  • The extract's mechanism involves membrane damage and disruption of biofilm matrix.
  • Identified bioactive compounds show potential for developing new phytotherapeutic strategies against biofilm-associated infections.
  • MKM extract represents a promising natural resource for combating antibiotic-resistant pathogens.

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