AI Article Synopsis

  • The text discusses a Gram-positive bacterium commonly found in the gastrointestinal tract that poses serious health risks as an opportunistic pathogen, particularly due to its multidrug resistance and ability to form biofilms.
  • The study evaluates the effectiveness of two juglone derivatives (2-methoxy-6-acetyl-7-methyljuglone and 2-ethoxy-6-acetyl-7-methyljuglone) against multidrug-resistant strains using various antibacterial tests and biofilm assessments.
  • Results indicate that the 2-ethoxy-6-acetyl-7-methyljuglone has superior antibacterial and antibiofilm properties compared to the other compound, showing promise for treating infections caused by this bacter

Article Abstract

is a Gram-positive bacterium that is normally found in the gastrointestinal tract of humans and animals. is an opportunistic pathogen that causes a number of invasive and noninvasive infections. The emergence of multidrug resistance and biofilm formation by the bacterium have rendered the treatment of infections very difficult. Due its high rate of resistance and biofilm formation, there are very few options of treatment. Therefore, the current study was designed to evaluate the antibacterial and biofilm activities of juglone derivatives such as 2-methoxy-6-acetyl-7-methyljuglone and 2-ethoxy-6-acetyl-7-methyljuglone against multidrug-resistant (MDR) and biofilm-producing strains of . Agar well diffusion and broth microdilution methods were used to determine the antibacterial activities. Biofilm attachment and preformed biofilm inhibition were determined using crystal violet staining assay. Both juglone derivatives displayed promising antibacterial and antibiofilm activities against . Among these compounds, 2-ethoxy-6-acetyl-7-methyljuglone possessed better inhibitory activity with minimum inhibitory concentration (MIC) of 9.7 ± 3 M as compared to 2-methoxy-6-acetyl-7-methyljuglone (MIC, 19.5 ± 2 M). Additionally, 2-ethoxy-6-acetyl-7-methyljuglone also showed stronger antibiofilm activity than 2-methoxy-6-acetyl-7-methyljuglone. Furthermore, both the ligand molecules were docked into the binding site of the enterococcal surface protein, and the results revealed that both the molecules are actively binding in the target site. Based on these findings, juglone derivatives may be considered useful for the treatment of infections; however, further studies are required to elucidate the mechanism of action.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9671725PMC
http://dx.doi.org/10.1155/2022/6197375DOI Listing

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