Targeting Iron - Respiratory Reciprocity Promotes Bacterial Death.
Mohammad Sharifian GhFatemeh NorouziMirco SorciTanweer S ZaidGerald B PierAlecia AchimovichGeorge M OngwaeBinyong LiangMargaret RyanMichael LemkeGeorges BelfortMihaela GadjevaAndreas GahlmannMarcos M PiresHenrietta VenterThurl E HarrisGordon W LauriePublished in: bioRxiv : the preprint server for biology (2024)
Discovering new bacterial signaling pathways offers unique antibiotic strategies. Here, through an unbiased resistance screen of 3,884 gene knockout strains, we uncovered a previously unknown non-lytic bactericidal mechanism that sequentially couples three transporters and downstream transcription to lethally suppress respiration of the highly virulent P. aeruginosa strain PA14 - one of three species on the WHO's 'Priority 1: Critical' list. By targeting outer membrane YaiW, cationic lacritin peptide 'N-104' translocates into the periplasm where it ligates outer loops 4 and 2 of the inner membrane transporters FeoB and PotH, respectively, to suppress both ferrous iron and polyamine uptake. This broadly shuts down transcription of many biofilm-associated genes, including ferrous iron-dependent TauD and ExbB1. The mechanism is innate to the surface of the eye and is enhanced by synergistic coupling with thrombin peptide GKY20. This is the first example of an inhibitor of multiple bacterial transporters.
Keyphrases
- genome wide
- iron deficiency
- immune response
- transcription factor
- signaling pathway
- cancer therapy
- pseudomonas aeruginosa
- genome wide identification
- staphylococcus aureus
- escherichia coli
- high throughput
- dna methylation
- drug delivery
- epithelial mesenchymal transition
- cell proliferation
- cystic fibrosis
- biofilm formation
- bioinformatics analysis
- genome wide analysis
- induced apoptosis