G-quadruplex motifs in Neisseria gonorrhoeae as anti-gonococcal targets.
Neha JainUma ShankarAakriti SinghTarun Kumar SharmaAmit KumarPublished in: Applied microbiology and biotechnology (2023)
Neisseria gonorrhoeae is an obligate human pathogen that causes gonorrhea and has shown a vast emergence of multidrug resistance in recent times. It is necessary to develop novel therapeutic strategies to combat this multidrug-resistant pathogen. The non-canonical stable secondary structures of nucleic acids, G-quadruplexes (GQs), are reported to regulate gene expressions in viruses, prokaryotes, and eukaryotes. Herein, we explored the whole genome of N. gonorrhoeae to mine evolutionary conserved GQ motifs. The Ng-GQs were highly enriched in the genes involved in various important biological and molecular processes of N. gonorrhoeae. Five of these GQ motifs were characterized using biophysical and biomolecular techniques. The GQ-specific ligand, BRACO-19, showed a high affinity towards these GQ motifs and stabilized them in both in vitro and in vivo conditions. The ligand showed potent anti-gonococcal activity and modulated the gene expression of the GQ-harboring genes. Strikingly, BRACO-19 also altered the biofilm formation in N. gonorrhoeae and its adhesion and invasion of the human cervical epithelial cells. In summary, the present study showed a significant role of GQ motifs in N. gonorrhoeae biology and put forward a step closer towards the search for therapeutic measures in combating the emerging antimicrobial resistance in the pathogen. KEY POINTS: •Neisseria gonorrhoeae genome is enriched in non-canonical nucleic acid structures-G-quadruplexes. •These G-quadruplexes might regulate bacterial growth, virulence, and pathogenesis. •G-quadruplex ligands inhibit biofilm formation, adhesion, and invasion of the gonococcus bacterium.
Keyphrases
- biofilm formation
- candida albicans
- pseudomonas aeruginosa
- staphylococcus aureus
- antimicrobial resistance
- escherichia coli
- gene expression
- genome wide
- endothelial cells
- multidrug resistant
- nucleic acid
- dna methylation
- induced pluripotent stem cells
- high resolution
- cell migration
- cystic fibrosis
- acinetobacter baumannii
- pluripotent stem cells
- genome wide identification
- drug resistant
- transcription factor
- mass spectrometry
- genome wide analysis
- genetic diversity