Preventative treatment with Fluorothiazinon suppressed Acinetobacter baumannii-associated septicemia in mice.
Nataliya E BondarevaAnna V SolovevaAnna B SheremetEkaterina A KorolevaLidiya N KapotinaElena Y MorgunovaSergei I LuyksaarEgor S ZayakinNailya A ZigangirovaPublished in: The Journal of antibiotics (2022)
The high prevalence of multidrug-resistant Acinetobacter baumannii has emerged as a serious problem in the treatment of nosocomial infections in the past three decades. Recently, we developed a new small-molecule inhibitor belonging to a class of 2,4-disubstituted-4H-[1,3,4]-thiadiazine-5-ones, Fluorothiazinon (FT, previously called CL-55). FT effectively suppressed the T3SS of Chlamydia spp., Pseudomonas aeruginosa, and Salmonella sp. without affecting bacterial growth in vitro. In this study, we describe that prophylactic use of FT for 4 days prior to challenge with resistant clinical isolates of A. baumannii (ABT-897-17 and 52TS19) suppressed septic infection in mice, resulting in improved survival, limited bacteraemia and decreased bacterial load in the organs of the mice. We show that FT had an inhibitory effect on A. baumannii biofilm formation in vitro and, to a greater extent, on biofilm maturation. In addition, FT inhibited Acinetobacter isolate-induced death of HeLa cells, which morphologically manifested as apoptosis. The mechanism of FT action on A. baumannii is currently being studied. FT may be a promising candidate for the development of a broad-spectrum anti-virulence drug to use in the prevention of nosocomial infections.
Keyphrases
- acinetobacter baumannii
- pseudomonas aeruginosa
- biofilm formation
- multidrug resistant
- cystic fibrosis
- drug resistant
- small molecule
- cell cycle arrest
- escherichia coli
- gram negative
- staphylococcus aureus
- acute kidney injury
- induced apoptosis
- type diabetes
- oxidative stress
- endoplasmic reticulum stress
- cell death
- replacement therapy