Glucose metabolism in the pathogenic free‐living amoebae: Tempting targets for treatment development

Author:

Milanes Jillian E.1,Kwain Samuel2ORCID,Drawdy Allyson1,Dodson Laura1,Monaghan Matthew T.1,Rice Christopher A.345,Dominy Brian N.6,Whitehead Daniel C.2ORCID,Morris James C.1

Affiliation:

1. Department of Genetics and Biochemistry, Eukaryotic Pathogens Innovation Center Clemson University Clemson South Carolina USA

2. Department of Chemistry, Eukaryotic Pathogens Innovation Center Clemson University Clemson South Carolina USA

3. Department of Comparative Pathobiology, College of Veterinary Medicine Purdue University West Lafayette Indiana USA

4. Purdue Institute for Drug Discovery (PIDD), Purdue University West Lafayette Indiana USA

5. Purdue Institute of Inflammation, Immunology and Infectious Disease (PI4D) Purdue University West Lafayette Indiana USA

6. Department of Chemistry Clemson University Clemson South Carolina USA

Abstract

AbstractPathogenic 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.

Funder

Clemson University

National Institutes of Health

Publisher

Wiley

Subject

Molecular Medicine,Biochemistry,Drug Discovery,Pharmacology,Organic Chemistry

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