Abstract

Multiple drug resistant (MDR) and methicillin-resistant Staphylococcus aureus (MRSA) have become increasingly prevalent as a community acquired infection. As a result limited treatment options are available with conventional synthetic antibiotics. Bioprospecting natural products with potent antimicrobial activity show promise for developing new drugs against this pathogen. In this study, we have investigated the antimicrobial activity of a purple violet pigment (PVP) from an Antarctic bacterium, Janthinobacterium sp. Ant5-2 on 15 clinical MDR and MRSA strains. The colorimetric resazurin assay was employed to determine the minimum inhibitory concentration (MIC90) of PVP against MDR and MRSA. The MIC90 ranged between 1.57 µg/mL and 3.13 µg/mL, which are significantly lower than many antimicrobials tested from natural sources against this pathogen. The spectrophotometrically determined growth analysis and total microscopic counts using Live/dead® BacLight™ fluorescent stain exhibited a steady decrease in viability of both MDR and MRSA cultures following treatment with PVP at the MIC levels. In silico predictive molecular docking study revealed that PVP could be a DNA-targeting minor groove binding antimicrobial compound. The continued development of novel antimicrobials derived from natural sources with the combination of a suite of conventional antibiotics could stem the rising pandemic of MDR and MRSA along with other deadly microbial pathogens.

Highlights

  • Staphylococcus aureus is an opportunistic human pathogen and recognized as the leading overall cause of hospitalacquired infections worldwide

  • In this study we describe the efficacy of purple violet pigment (PVP) as an antimicrobial for multiple drug resistant (MDR) and methicillin-resistant Staphylococcus aureus (MRSA) strains of S. aureus and a comparison of the minimum inhibitory concentration (MIC) of PVP with previously reported other antimicrobials from natural sources as well the synthetic antibiotics

  • An increasing trend of the MDR and MRSA-related infections and mortality in humans with limited options of treatment using conventional antibiotics led to the identification of novel antimicrobial compounds that are

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Summary

Introduction

Staphylococcus aureus is an opportunistic human pathogen and recognized as the leading overall cause of hospitalacquired infections worldwide. Ant[] on virulent and avirulent strains of Mycobacterium tuberculosis.[20] In this study we describe the efficacy of PVP as an antimicrobial for MDR and MRSA strains of S. aureus and a comparison of the MICs of PVP with previously reported other antimicrobials from natural sources as well the synthetic antibiotics.

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