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Friend or Foe? Implication of the Autophagy-lysosome Pathway in SARS-CoV-2 Infection and COVID-19

Overview
Journal Int J Biol Sci
Specialty Biology
Date 2022 Jul 25
PMID 35874956
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Abstract

There is increasing amount of evidence indicating the close interplays between the replication cycle of SARS-CoV-2 and the autophagy-lysosome pathway in the host cells. While autophagy machinery is known to either assist or inhibit the viral replication process, the reciprocal effects of the SARS-CoV-2 on the autophagy-lysosome pathway have also been increasingly appreciated. More importantly, despite the disappointing results from the clinical trials of chloroquine and hydroxychloroquine in treatment of COVID-19, there is still ongoing effort in discovering new therapeutics targeting the autophagy-lysosome pathway. In this review, we provide an update-to-date summary of the interplays between the autophagy-lysosome pathway in the host cells and the pathogen SARS-CoV-2 at the molecular level, to highlight the prognostic value of autophagy markers in COVID-19 patients and to discuss the potential of developing novel therapeutic strategies for COVID-19 by targeting the autophagy-lysosome pathway. Thus, understanding the nature of such interactions between SARS-CoV-2 and the autophagy-lysosome pathway in the host cells is expected to provide novel strategies in battling against this global pandemic.

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References
1.
Molejon M, Ropolo A, Vaccaro M . VMP1 is a new player in the regulation of the autophagy-specific phosphatidylinositol 3-kinase complex activation. Autophagy. 2013; 9(6):933-5. PMC: 3672306. DOI: 10.4161/auto.24390. View

2.
Chen Y, Li M, Lu G, Shen H, Zhou J . Hydroxychloroquine/Chloroquine as Therapeutics for COVID-19: Truth under the Mystery. Int J Biol Sci. 2021; 17(6):1538-1546. PMC: 8071775. DOI: 10.7150/ijbs.59547. View

3.
Booth L, Roberts J, Ecroyd H, Tritsch S, Bavari S, Reid S . AR-12 Inhibits Multiple Chaperones Concomitant With Stimulating Autophagosome Formation Collectively Preventing Virus Replication. J Cell Physiol. 2016; 231(10):2286-302. PMC: 6327852. DOI: 10.1002/jcp.25431. View

4.
Ghosh S, Dellibovi-Ragheb T, Kerviel A, Pak E, Qiu Q, Fisher M . β-Coronaviruses Use Lysosomes for Egress Instead of the Biosynthetic Secretory Pathway. Cell. 2020; 183(6):1520-1535.e14. PMC: 7590812. DOI: 10.1016/j.cell.2020.10.039. View

5.
Gendrot M, Duflot I, Boxberger M, Delandre O, Jardot P, Bideau M . Antimalarial artemisinin-based combination therapies (ACT) and COVID-19 in Africa: In vitro inhibition of SARS-CoV-2 replication by mefloquine-artesunate. Int J Infect Dis. 2020; 99:437-440. PMC: 7426697. DOI: 10.1016/j.ijid.2020.08.032. View