Frontiers in Bioinformatics (Jul 2024)

Predictive identification and design of potent inhibitors targeting resistance-inducing candidate genes from E. coli whole-genome sequences

  • Abdullahi Tunde Aborode,
  • Neeraj Kumar,
  • Christopher Busayo Olowosoke,
  • Christopher Busayo Olowosoke,
  • Tope Abraham Ibisanmi,
  • Islamiyyah Ayoade,
  • Islamiyyah Ayoade,
  • Haruna Isiyaku Umar,
  • Haruna Isiyaku Umar,
  • Abdullahi Temitope Jamiu,
  • Basit Bolarinwa,
  • Zainab Olapade,
  • Abidemi Ruth Idowu,
  • Ibrahim O. Adelakun,
  • Isreal Ayobami Onifade,
  • Benjamin Akangbe,
  • Modesta Abacheng,
  • Odion O. Ikhimiukor,
  • Aeshah A. Awaji,
  • Ridwan Olamilekan Adesola

DOI
https://doi.org/10.3389/fbinf.2024.1411935
Journal volume & issue
Vol. 4

Abstract

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Introduction: This work utilizes predictive modeling in drug discovery to unravel potential candidate genes from Escherichia coli that are implicated in antimicrobial resistance; we subsequently target the gidB, MacB, and KatG genes with some compounds from plants with reported antibacterial potentials.Method: The resistance genes and plasmids were identified from 10 whole-genome sequence datasets of E. coli; forty two plant compounds were selected, and their 3D structures were retrieved and optimized for docking. The 3D crystal structures of KatG, MacB, and gidB were retrieved and prepared for molecular docking, molecular dynamics simulations, and ADMET profiling.Result: Hesperidin showed the least binding energy (kcal/mol) against KatG (−9.3), MacB (−10.7), and gidB (−6.7); additionally, good pharmacokinetic profiles and structure–dynamics integrity with their respective protein complexes were observed.Conclusion: Although these findings suggest hesperidin as a potential inhibitor against MacB, gidB, and KatG in E. coli, further validations through in vitro and in vivo experiments are needed. This research is expected to provide an alternative avenue for addressing existing antimicrobial resistances associated with E. coli’s MacB, gidB, and KatG.

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