Elucidation of Antiviral and Antioxidant Potential of C-Phycocyanin against HIV-1 Infection through <i>In Silico</i> and <i>In Vitro</i> Approaches

Antiretroviral therapy is the single existing therapy for patients infected with HIV; however, it has drawbacks in terms of toxicity and resistance. Thus, there is a continuous need to explore safe and efficacious anti-retroviral agents. C-Phycocyanin (C-PC) is a phycobiliprotein, which has been kno...

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Main Authors: Pratiksha Jadaun (Author), Chandrabhan Seniya (Author), Sudhir Kumar Pal (Author), Sanjit Kumar (Author), Pramod Kumar (Author), Vijay Nema (Author), Smita S Kulkarni (Author), Anupam Mukherjee (Author)
Format: Book
Published: MDPI AG, 2022-09-01T00:00:00Z.
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Summary:Antiretroviral therapy is the single existing therapy for patients infected with HIV; however, it has drawbacks in terms of toxicity and resistance. Thus, there is a continuous need to explore safe and efficacious anti-retroviral agents. C-Phycocyanin (C-PC) is a phycobiliprotein, which has been known for various biological properties; however, its effect on HIV-1 replication needs revelation. This study aimed to identify the inhibitory effects of C-PC on HIV-1 using <i>in vitro</i> and <i>in silico</i> approaches and to assess its role in the generation of mitochondrial reactive oxygen species (ROS) during HIV-1 infection. <i>In vitro</i> anti-HIV-1 activity of C-PC was assessed on TZM-bl cells through luciferase gene assay against four different clades of HIV-1 strains in a dose-dependent manner. Results were confirmed in PBMCs, using the HIV-1 p24 antigen assay. Strong associations between C-PC and HIV-1 proteins were observed through <i>in silico</i> molecular simulation-based interactions, and the <i>in vitro</i> mechanistic study confirmed its target by inhibition of reverse transcriptase and protease enzymes. Additionally, the generation of mitochondrial ROS was detected by the MitoSOX and DCF-DA probe through confocal microscopy. Furthermore, our results confirmed that C-PC treatment notably subdued the fluorescence in the presence of the virus, thus reduction of ROS and the activation of caspase-3/7 in HIV-1-infected cells. Overall, our study suggests C-PC as a potent and broad <i>in vitro</i> antiviral and antioxidant agent against HIV-1 infection.
Item Description:10.3390/antiox11101942
2076-3921