Lipophilic prodrugs of FR900098 are antimicrobial against Francisella novicida in vivo and in vitro and show GlpT independent efficacy

• Published in: PloS one 2012-10, Vol.7 (10), p.e38167
• Main Authors: McKenney, Elizabeth S, Sargent, Michelle, Khan, Hameed, Uh, Eugene, Jackson, Emily R, San Jose, Géraldine, Couch, Robin D, Dowd, Cynthia S, van Hoek, Monique L
• Format: Article
• Language: English
• Subjects: Algae; Analysis; Animals; Anti-Bacterial Agents - pharmacology; Anti-infective agents; Antibiotics; Antiinfectives and antibacterials; Antimicrobial activity; Antimicrobial agents; Bacteria; Bacterial Proteins - metabolism; Biochemistry; Biology; Burkholderia; Catalysis; Cell Line; Cell lines; Cell walls; Cells (Biology); Chemical compounds; Chemistry; D-Xylulose 5-phosphate; Dosage and administration; Drug development; Drug resistance; Drug therapy; Drugs; E coli; Escherichia coli; Eukaryotes; Evaluation; Fosfomycin - analogs & derivatives; Fosfomycin - pharmacology; Fosmidomycin; Francisella - drug effects; Francisella tularensis; Genes; Genetic aspects; Glycerol; Health aspects; Homology; Humans; Infections; Infectious diseases; Inhibitory Concentration 50; Lipophilic; Medicine; Mice; Microbial Sensitivity Tests; Mutants; Mutation; Phosphates; Plants (botany); Prodrugs; Prodrugs - pharmacology; Prokaryotes; Reductoisomerase; Signal transduction; Terpenes; Transposons; Tuberculosis; Veterinary Science; Xylulose
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0038167

Bacteria, plants, and algae produce isoprenoids through the methylerythritol phosphate (MEP) pathway, an attractive pathway for antimicrobial drug development as it is present in prokaryotes and some lower eukaryotes but absent from human cells. The first committed step of the MEP pathway is catalyzed by 1-deoxy-D-xylulose 5-phosphate reductoisomerase (DXR/MEP synthase). MEP pathway genes have been identified in many biothreat agents, including Francisella, Brucella, Bacillus, Burkholderia, and Yersinia. The importance of the MEP pathway to Francisella is demonstrated by the fact that MEP pathway mutations are lethal. We have previously established that fosmidomycin inhibits purified MEP synthase (DXR) from F. tularensis LVS. FR900098, the acetyl derivative of fosmidomycin, was found to inhibit the activity of purified DXR from F. tularensis LVS (IC(50)=230 nM). Fosmidomycin and FR900098 are effective against purified DXR from Mycobacterium tuberculosis as well, but have no effect on whole cells because the compounds are too polar to penetrate the thick cell wall. Fosmidomycin requires the GlpT transporter to enter cells, and this is absent in some pathogens, including M. tuberculosis. In this study, we have identified the GlpT homologs in F. novicida and tested transposon insertion mutants of glpT. We showed that FR900098 also requires GlpT for full activity against F. novicida. Thus, we synthesized several FR900098 prodrugs that have lipophilic groups to facilitate their passage through the bacterial cell wall and bypass the requirement for the GlpT transporter. One compound, that we termed "compound 1," was found to have GlpT-independent antimicrobial activity. We tested the ability of this best performing prodrug to inhibit F. novicida intracellular infection of eukaryotic cell lines and the caterpillar Galleria mellonella as an in vivo infection model. As a lipophilic GlpT-independent DXR inhibitor, compound 1 has the potential to be a broad-spectrum antibiotic, and should be effective against most MEP-dependent organisms.