figshare
Browse
DOCUMENT
S1_Fig.pdf (45.07 kB)
DOCUMENT
S2_Fig.pdf (45.51 kB)
DOCUMENT
S3_Fig.pdf (231.13 kB)
DOCUMENT
S4_Fig.pdf (275.58 kB)
DOCUMENT
S1_Supporting_Information.pdf (115.35 kB)
DOCUMENT
S2_Supporting_Information.pdf (563.12 kB)
DOCUMENT
S3_Supporting_Information.pdf (103.8 kB)
DOCUMENT
S4_Supporting_Information.pdf (472.41 kB)
DOCUMENT
S1_Table.pdf (31.65 kB)
DOCUMENT
S2_Table.pdf (34.65 kB)
1/0
10 files

Insights into the Mechanism of Action of Bactericidal Lipophosphonoxins

dataset
posted on 2016-01-05, 14:53 authored by Natalya Panova, Eva Zborníková, Ondřej Šimák, Radek Pohl, Milan Kolar, Katerina Bogdanova, Renata Vecerova, Gabriela Seydlová, Radovan Fiser, Romana Hadravová, Hana Šanderová, Dragana Vítovská, Michaela Šiková, Tomáš Látal, Petra Lovecká, Ivan Barvík, Libor Krásný, Dominik Rejman

The advantages offered by established antibiotics in the treatment of infectious diseases are endangered due to the increase in the number of antibiotic-resistant bacterial strains. This leads to a need for new antibacterial compounds. Recently, we discovered a series of compounds termed lipophosphonoxins (LPPOs) that exhibit selective cytotoxicity towards Gram-positive bacteria that include pathogens and resistant strains. For further development of these compounds, it was necessary to identify the mechanism of their action and characterize their interaction with eukaryotic cells/organisms in more detail. Here, we show that at their bactericidal concentrations LPPOs localize to the plasmatic membrane in bacteria but not in eukaryotes. In an in vitro system we demonstrate that LPPOs create pores in the membrane. This provides an explanation of their action in vivo where they cause serious damage of the cellular membrane, efflux of the cytosol, and cell disintegration. Further, we show that (i) LPPOs are not genotoxic as determined by the Ames test, (ii) do not cross a monolayer of Caco-2 cells, suggesting they are unable of transepithelial transport, (iii) are well tolerated by living mice when administered orally but not peritoneally, and (iv) are stable at low pH, indicating they could survive the acidic environment in the stomach. Finally, using one of the most potent LPPOs, we attempted and failed to select resistant strains against this compound while we were able to readily select resistant strains against a known antibiotic, rifampicin. In summary, LPPOs represent a new class of compounds with a potential for development as antibacterial agents for topical applications and perhaps also for treatment of gastrointestinal infections.

History

Usage metrics

    PLOS ONE

    Licence

    Exports

    RefWorks
    BibTeX
    Ref. manager
    Endnote
    DataCite
    NLM
    DC