HIV-1 Integrase Inhibition Activity by Spiroketals Derived from Plagius flosculosus, an Endemic Plant of Sardinia (Italy) and Corsica (France)

Author:

Sanna Cinzia1ORCID,D’Abrosca Brigida2ORCID,Fiorentino Antonio2ORCID,Giammarino Federica3,Vicenti Ilaria3ORCID,Corona Angela4ORCID,Caredda Alessia4,Tramontano Enzo4ORCID,Esposito Francesca4ORCID

Affiliation:

1. Department of Life and Environmental Sciences, University of Cagliari, Via Sant’Ignazio da Laconi 13, 09123 Cagliari, Italy

2. Department of Environmental Biological and Pharmaceutical Sciences and Technologies, DiSTABiF University of Campania Luigi Vanvitelli, Via Vivaldi 43, 81100 Caserta, Italy

3. Department of Medical Biotechnologies, University of Siena, Viale Bracci 16, 53100 Siena, Italy

4. Department of Life and Environmental Sciences, University of Cagliari, Cittadella Universitaria di Monserrato, SS554, 09042 Monserrato, Italy

Abstract

In this work we investigated, for the first time, the effect of Plagius flosculosus (L.) Alavi & Heywood, a Sardinian–Corsican endemic plant, on HIV-1 integrase (IN) activity. The phytochemical analysis of the leaves chloroform extract led us to isolate and characterize three compounds (SPK1, SPK2, and SPK3) belonging to the spiroketals, a group of naturally occurring metabolites of phytochemical relevance with interesting biological properties. Due to their structural diversity, these cyclic ketals have attracted the interest of chemists and biologists. SPK1, SPK2, and SPK3 were evaluated here for their ability to inhibit HIV-1 integrase activity in biochemical assays. The results showed that all the compounds inhibited HIV-1 IN activity. In particular, the most active one was SPK3, which interfered in a low molecular range (IC50 of 1.46 ± 0.16 µM) with HIV-1 IN activity in the presence/absence of the LEDGF cellular cofactor. To investigate the mechanism of action, the three spiroketals were also tested on HIV-1 RT-associated Ribonuclease H (RNase H) activity, proving to be active in inhibiting this function. Although SPK3 was unable to inhibit viral replication in cell culture, it promoted the IN multimerization. We hypothesize that SPK3 inhibited HIV-1 IN through an allosteric mechanism of action.

Publisher

MDPI AG

Subject

Drug Discovery,Pharmaceutical Science,Molecular Medicine

Reference48 articles.

1. Fact Sheet—Latest Global and Regional Statistics on the Status of the AIDS Epidemic (2023, April 03). UNAIDS. Available online: https://www.unaids.org/en/resources/documents/2022/UNAIDS_FactSheet.

2. HIV-1 Reverse Transcription;Hu;Cold Spring Harb. Perspect. Med.,2012

3. Recombining the Structures of HIV Integrase, RuvC and RNase H The Recently Reported Crystal Structures of Two Recombination Enzymes, Endonuclease, Are Surprisingly Similar to That of Ribonuclease H Suggesting the Possibility That They Have a Common Enz;Yang;Structure,1995

4. Integrase and Integration: Biochemical Activities of HIV-1 Integrase;Delelis;Retrovirology,2008

5. Allosteric Inhibition of HIV-1 Integrase Activity;Engelman;Curr. Opin. Chem. Biol.,2013

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