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Extracts as a Potential Antibacterial Inhibitors against Clinical Isolates of : An In-Silico-Supported In-Vitro Study. | LitMetric

Extracts as a Potential Antibacterial Inhibitors against Clinical Isolates of : An In-Silico-Supported In-Vitro Study.

Antibiotics (Basel)

Department of Pathology, College of Medicine, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia.

Published: September 2021

AI Article Synopsis

  • Imipenem is a highly effective antibiotic, but bacteria have developed resistance, prompting researchers to explore alternatives through molecular studies and antibacterial activity assessments.
  • A total of 110 clinical isolates were analyzed, revealing multidrug-resistance and promising results for the ethanolic extract of guanosine against the resistant strains.
  • In silico studies demonstrated that guanosine and other compounds showed favorable interactions and higher binding affinity to Penicillin-binding proteins, suggesting potential as effective treatments compared to imipenem.

Article Abstract

Imipenem is the most efficient antibiotic against infection, but new research has shown that the organism has also developed resistance to this agent. isolates from a total of 110 clinical samples were identified by multiplex PCR. The antibacterial activity of multiple extracts was assessed following the GC-Mass spectra analysis. The molecular docking study was performed to investigate the binding mode of interactions of guanosine (Ethanolic extract compound) against Penicillin- binding proteins 1 and 3 of . Ten isolates of were confirmed to carry A and A genes. Isolates were multidrug-resistant containing and . The concentrations (0.04 to 0.125 mg mL) of ethanolic extract were very promising against isolates. Even though imipenem (0.02 mg mL) individually showed a great bactericidal efficacy against all isolates, the in-silico study of guanosine, apioline, eugenol, and elemicin showed acceptable fitting to the binding site of the PBP1 and/or PBP3 with highest binding energy for guanosine between -7.1 and -8.1 kcal/mol respectively. Moreover, it formed π-stacked interactions with the residue ARG76 at 4.14 and 5.6, Å respectively. These findings might support the in vitro study and show a substantial increase in binding affinity and enhanced physicochemical characteristics compared to imipenem.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8472170PMC
http://dx.doi.org/10.3390/antibiotics10091062DOI Listing

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