HIV infection and latency induce a unique metabolic signature in human macrophages View Full Text


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Article Info

DATE

2019-12

AUTHORS

Paul Castellano, Lisa Prevedel, Silvana Valdebenito, Eliseo A. Eugenin

ABSTRACT

Currently, a major barrier to curing HIV infection is the generation of tissue-associated, non-replicating, long-lasting viral reservoirs that are refractory to therapy and can be reactivated upon anti-retroviral therapy interruption. One of these reservoirs are latently HIV-infected macrophages. Here, we show that HIV infection of macrophages results in survival of a small population of infected cells that are metabolically altered and characterized by mitochondrial fusion, lipid accumulation, and reduced mitochondrial ATP production. No changes in glycolysis were detected. Metabolic analysis indicated an essential role of succinate and other TCA metabolites in the tricarboxylic acid (TCA) cycle in mediating lipid accumulation and oxidative phosphorylation (OXPHOS) in the mitochondria. Furthermore, we show that while uninfected and HIV infected macrophages use fatty acids and glucose as primary sources of energy, surviving HIV infected macrophages also use glutamine/glutamate as a major energy source, and blocking these new sources of energy resulted in the killing of latent HIV infected macrophages. Together, our data provide a new understanding of the formation, properties, and potential novel ways to eliminate macrophage viral reservoirs. More... »

PAGES

3941

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  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1038/s41598-019-39898-5

    DOI

    http://dx.doi.org/10.1038/s41598-019-39898-5

    DIMENSIONS

    https://app.dimensions.ai/details/publication/pub.1112641491

    PUBMED

    https://www.ncbi.nlm.nih.gov/pubmed/30850623


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    RDF/XML is a standard XML format for linked data.

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