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Glucose metabolism in the pathogenic free-living amoebae: Tempting targets for treatment development.
Milanes, Jillian E; Kwain, Samuel; Drawdy, Allyson; Dodson, Laura; Monaghan, Matthew T; Rice, Christopher A; Dominy, Brian N; Whitehead, Daniel C; Morris, James C.
Affiliation
  • Milanes JE; Department of Genetics and Biochemistry, Eukaryotic Pathogens Innovation Center, Clemson University, Clemson, South Carolina, USA.
  • Kwain S; Department of Chemistry, Eukaryotic Pathogens Innovation Center, Clemson University, Clemson, South Carolina, USA.
  • Drawdy A; Department of Genetics and Biochemistry, Eukaryotic Pathogens Innovation Center, Clemson University, Clemson, South Carolina, USA.
  • Dodson L; Department of Genetics and Biochemistry, Eukaryotic Pathogens Innovation Center, Clemson University, Clemson, South Carolina, USA.
  • Monaghan MT; Department of Genetics and Biochemistry, Eukaryotic Pathogens Innovation Center, Clemson University, Clemson, South Carolina, USA.
  • Rice CA; Department of Comparative Pathobiology, College of Veterinary Medicine, Purdue University, West Lafayette, Indiana, USA.
  • Dominy BN; Purdue Institute for Drug Discovery (PIDD), Purdue University, West Lafayette, Indiana, USA.
  • Whitehead DC; Purdue Institute of Inflammation, Immunology and Infectious Disease (PI4D), Purdue University, West Lafayette, Indiana, USA.
  • Morris JC; Department of Chemistry, Clemson University, Clemson, South Carolina, USA.
Chem Biol Drug Des ; 103(1): e14377, 2024 01.
Article in En | MEDLINE | ID: mdl-37864277
Pathogenic free-living amoebae (pFLA) are single-celled eukaryotes responsible for causing intractable infections with high morbidity and mortality in humans and animals. Current therapeutic approaches include cocktails of antibiotic, antifungal, and antimicrobial compounds. Unfortunately, the efficacy of these can be limited, driving the need for the discovery of new treatments. Pan anti-amebic agents would be ideal; however, identifying these agents has been a challenge, likely due to the limited evolutionary relatedness of the different pFLA. Here, we discuss the potential of targeting amoebae glucose metabolic pathways as the differences between pFLA and humans suggest specific inhibitors could be developed as leads for new therapeutics.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Amoeba Limits: Animals / Humans Language: En Journal: Chem Biol Drug Des Journal subject: BIOQUIMICA / FARMACIA / FARMACOLOGIA Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Amoeba Limits: Animals / Humans Language: En Journal: Chem Biol Drug Des Journal subject: BIOQUIMICA / FARMACIA / FARMACOLOGIA Year: 2024 Document type: Article Affiliation country: Country of publication: