Table 1.
Major types of antimicrobial compounds with their mechanisms of action.
Future therapy | Mechanism | Contemporary strategies to improve activity |
---|---|---|
Antimicrobial peptides | Attach and insert into membrane bilayers to form pores by “barrel-stave,” “carpet,” or “toroidal-pore” mechanisms. DNA and macromolecule synthesis inhibitors. | Optimization of peptide length and content of their sequences. |
Conversion into peptidomimetics. | ||
Generation of targeted antimicrobial peptides (Peptide antibiotic conjugation). | ||
Generation of antimicrobial peptides as prodrug candidates. | ||
Antimicrobial peptides loaded into nanoparticle or micelles for sustained release. | ||
Phage therapy | Bacteriophages are viruses that act as pathogens against bacteria and completely lyse the bacteria. | Genetically engineered phages. |
Genetically engineered phase as antibiotic delivery. | ||
Engineered bacteriophage for phage targeted drug delivery. | ||
Scale up of endolysin production. | ||
Phytochemicals | Multiple actions. | Search for novel compounds and cost-effective methods of extraction and purification of phytochemical. |
Transgenic production in plant and microbial system to enhance number of novel compounds. | ||
Search for endophytic fungal metabolomics for the production of novel compound of host. | ||
Synthesis and modification of natural structure and analogs. | ||
Metalloantibiotic | Increased spectrum of conventional antibiotic action. | Synthetic or semi-synthetic antimicrobial compound development attaching metal to its structure. |
In situ reducing and capping of metal nanoparticle with enhanced antimicrobial activity. | ||
Efflux pump inhibitor | Molecules to inhibit the active protein pump in the bacterial cell. | Chemical synthesis of effective efflux pumps inhibitor. |
Screening of efflux pump inhibitors from natural origin and modifying this compound synthetically. | ||
Rationally designed transmembrane peptide mimics. |