# Selective in vitro Synergistic Evaluation of Probiotic Tolerant morpholinyl- and 4-ethylpiperazinyl-Imidazole-chalcone Derivatives on Gastrointestinal System Pathogens

**Authors:** Tuncay Söylemez, Zafer Asım Kaplancıklı, Derya Osmaniye, Yusuf Özkay, Fatih Demirci

PMC · DOI: 10.1007/s00284-024-03788-5 · Current Microbiology · 2024-07-03

## TL;DR

This study identifies imidazole-chalcone compounds that are safe for probiotics and show antimicrobial effects against gut pathogens.

## Contribution

The study is the first to report the fractional inhibitory concentration of imidazole-chalcone combinations against pathogens.

## Key findings

- Four imidazole-chalcone derivatives were probiotic-tolerant and showed antibacterial and antifungal activity.
- Morpholinyl- and 4-ethylpiperazinyl derivatives had low MIC values against E. coli and B. subtilis.
- The combination of derivatives showed additive effects against B. subtilis but indifferent effects against E. coli.

## Abstract

Imidazole-chalcone compounds are recognised for their broad-spectrum antimicrobial properties. Probiotic-friendly, selective new-generation antimicrobials prove to be more efficient in combating gastrointestinal system pathogens. The aim of this study is to identify imidazole-chalcone derivatives that probiotics tolerate and evaluate their in vitro synergistic antimicrobial effects on pathogens. In this study, fifteen previously identified imidazole-chalcone derivatives were analyzed for their in vitro antimicrobial properties against gastrointestinal microorganisms. Initially, the antimicrobial activity of pathogens was measured using the agar well diffusion method, while the susceptibility of probiotics was determined by microdilution. The chosen imidazole-chalcone derivatives were assessed for synergistic effects using the checkerboard method. Four imidazole-chalcone derivatives to which probiotic bacteria were tolerant exhibited antibacterial and antifungal activity against the human pathogens tested. To our knowledge, this study is the first to reveal the fractional inhibitory concentration (FIC) of combinations of imidazole-chalcone derivatives. Indeed, the minimum inhibitory concentrations (MIC) for morpholinyl- (ZDO-3f) and 4-ethylpiperazinyl- (ZDO-3 m) imidazole-chalcones were notably low when tested against E. coli and B. subtilis, with values of 31.25 μg/mL and 125 μg/mL, respectively. The combination of morpholinyl- and 4-ethylpiperazinyl derivatives demonstrated an indifferent effect against E. coli, but an additive effect was observed for B. subtilis. Additionally, it was observed that imidazole-chalcone derivatives did not exhibit any inhibitory effects on probiotic organisms like Lactobacillus fermentum (CECT-5716), Lactobacillus rhamnosus (GG), and Lactobacillus casei (RSSK-591). This study demonstrates that imidazole-chalcone derivatives that are well tolerated by probiotics can potentially exert a synergistic effect against gastrointestinal system pathogens.

The online version contains supplementary material available at 10.1007/s00284-024-03788-5.

## Full-text entities

- **Species:** Lacticaseibacillus rhamnosus (species) [taxon 47715], Limosilactobacillus fermentum (species) [taxon 1613], Homo sapiens (human, species) [taxon 9606], Escherichia coli (E. coli, species) [taxon 562], Geobacillus sp. g (species) [taxon 422286], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Lacticaseibacillus casei (species) [taxon 1582], Bacillus subtilis (species) [taxon 1423]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC11222229