1. The cell division protein FtsZ as a cellular target to hit cystic fibrosis pathogens.
- Author
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Buroni S, Makarov V, Scoffone VC, Trespidi G, Riccardi G, and Chiarelli LR
- Subjects
- Anti-Bacterial Agents chemistry, Anti-Bacterial Agents therapeutic use, Cystic Fibrosis microbiology, Enzyme Inhibitors chemistry, Enzyme Inhibitors pharmacology, GTP Phosphohydrolases antagonists & inhibitors, Gram-Negative Bacteria drug effects, Humans, Staphylococcal Infections drug therapy, Staphylococcus aureus drug effects, Anti-Bacterial Agents pharmacology, Bacterial Proteins antagonists & inhibitors, Cytoskeletal Proteins antagonists & inhibitors
- Abstract
Cystic fibrosis is a rare genetic disease characterized by the production of dehydrated mucus in the lung able to trap bacteria and rendering their proliferation particularly dangerous, thus leading to chronic infections. Among these bacteria, Staphylococcus aureus and Pseudomonas aeruginosa play a major role while, within emerging pathogens, Stenotrophomonas maltophilia, Achromobacter xylosoxidans, Burkholderia cepacia complex species, as well as non-tuberculous mycobacteria are listed. Since a common feature of these bacteria is the high level of drug resistance, cell division, and in particular FtsZ, has been explored as a novel therapeutic target for the design of new molecules with antibacterial properties. This review summarizes and provides insight into recent advances in the discovery of compounds targeting FtsZ: the majority of them exhibit anti-staphylococcal activity, while a few were directed against the cystic fibrosis Gram negative pathogens., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier Masson SAS. All rights reserved.)
- Published
- 2020
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