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Review
. 2017 Feb 17;8(2):143-149.
doi: 10.1080/21505594.2016.1195529. Epub 2016 Jun 1.

Trehalose pathway as an antifungal target

Affiliations
Review

Trehalose pathway as an antifungal target

John R Perfect et al. Virulence. .

Abstract

With an increasing immunocompromised population which is linked to invasive fungal infections, it is clear that our present 3 classes of antifungal agents may not be sufficient to provide optimal management to these fragile patients. Furthermore, with widespread use of antifungal agents, drug-resistant fungal infections are on the rise. Therefore, there is some urgency to develop the antifungal pipeline with the goal of new antifungal agent discovery. In this review, a simple metabolic pathway, which forms the disaccharide, trehalose, will be characterized and its potential as a focus for antifungal target(s) explained. It possesses several important features for development of antifungal agents. First, it appears to have fungicidal characteristics and second, it is broad spectrum with importance across both ascomycete and basidiomycete species. Finally, this pathway is not found in mammals so theoretically specific inhibitors of the trehalose pathway and its enzymes in fungi should be relatively non-toxic for mammals. The trehalose pathway and its critical enzymes are now in a position to have directed antifungal discovery initiated in order to find a new class of antifungal drugs.

Keywords: antifungal; drug development; trehalose.

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Figures

Figure 1.
Figure 1.
The putative trehalose pathway in cryptococcus.

Comment in

  • Trehalose as antifungal target: The picture is still incomplete.
    Argüelles JC. Argüelles JC. Virulence. 2017 Feb 17;8(2):237-238. doi: 10.1080/21505594.2016.1215797. Epub 2016 Jul 26. Virulence. 2017. PMID: 27459134 Free PMC article. No abstract available.
  • Reply to Argüelles.
    Perfect JR. Perfect JR. Virulence. 2017 Feb 17;8(2):239. doi: 10.1080/21505594.2016.1221249. Epub 2016 Aug 5. Virulence. 2017. PMID: 27494147 Free PMC article. No abstract available.

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