Targeting autophagy with natural products to prevent SARS-CoV-2 infection

被引:23
作者
Vidoni, Chiara [1 ]
Fuzimoto, Andrea [2 ]
Ferraresi, Alessandra [1 ]
Isidoro, Ciro [1 ]
机构
[1] Univ Piemonte Orientale, Dept Hlth Sci, Novara, Italy
[2] Holist Sync, Holist Integrat Med, Washington, DC USA
关键词
COVID-19; Virophagy; Coronavirus; Chloroquine; Pandemic; Phytotherapy; Resveratrol; MOLECULAR-DYNAMICS; ANTIVIRAL ACTION; ARTEMISIA-ANNUA; IN-VITRO; VIRUS; REPLICATION; BAICALIN; CORONAVIRUSES; PROCYANIDIN; INHIBITION;
D O I
10.1016/j.jtcme.2021.10.003
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Autophagy is a catabolic process that maintains internal homeostasis and energy balance through the lysosomal degradation of redundant or damaged cellular components. During virus infection, autophagy is triggered both in parenchymal and in immune cells with different finalistic objectives: in parenchymal cells, the goal is to destroy the virion particle while in macrophages and dendritic cells the goal is to expose virion-derived fragments for priming the lymphocytes and initiate the immune response. However, some viruses have developed a strategy to subvert the autophagy machinery to escape the destructive destiny and instead exploit it for virion assembly and exocytosis. Coronaviruses (like SARS-CoV-2) possess such ability. The autophagy process requires a set of proteins that constitute the core machinery and is controlled by several signaling pathways. Here, we report on natural products capable of interfering with SARS-CoV-2 cellular infection and replication through their action on autophagy. The present study provides support to the use of such natural products as adjuvant therapeutics for the management of COVID-19 pandemic to prevent the virus infection and replication, and so mitigating the progression of the disease. (c) 2021 Center for Food and Biomolecules, National Taiwan University. Production and hosting by Elsevier Taiwan LLC. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/ licenses/by-nc-nd/4.0/).
引用
收藏
页码:55 / 68
页数:14
相关论文
共 122 条
[1]   Antiviral Activity of Resveratrol against Human and Animal Viruses [J].
Abba, Yusuf ;
Hassim, Hasliza ;
Hamzah, Hazilawati ;
Noordin, Mohamed Mustapha .
ADVANCES IN VIROLOGY, 2015, 2015
[2]  
Abe A., 2016, AUTOPHAGY, V12, P1, DOI [DOI 10.1080/15548627.2015.1100356, 10.1080/15548627.2015.1100356]
[3]   Structural stability of SARS-CoV-2 3CLpro and identification of quercetin as an inhibitor by experimental screening [J].
Abian, Olga ;
Ortega-Alarcon, David ;
Jimenez-Alesanco, Ana ;
Ceballos-Laita, Laura ;
Vega, Sonia ;
Reyburn, Hugh T. ;
Rizzuti, Bruno ;
Velazquez-Campoy, Adrian .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2020, 164 :1693-1703
[4]   Inhibition of angiotensin converting enzyme (ACE) activity by flavan-3-ols and procyanidins [J].
Actis-Goretta, L ;
Ottaviani, JI ;
Keen, CL ;
Fraga, CG .
FEBS LETTERS, 2003, 555 (03) :597-600
[5]   Implications of the Novel Mutations in the SARS-CoV-2 Genome for Transmission, Disease Severity, and the Vaccine Development [J].
Akkiz, Hikmet .
FRONTIERS IN MEDICINE, 2021, 8
[6]   Molecular regulation of autophagy machinery by mTOR-dependent and -independent pathways [J].
Al-Bari, Md Abdul Alim ;
Xu, Pingyong .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 2020, 1467 (01) :3-20
[7]   Ethnomedicines of Indian origin for combating COVID-19 infection by hampering the viral replication: using structure-based drug discovery approach [J].
Alagu Lakshmi, Selvaraj ;
Shafreen, Raja Mohamed Beema ;
Priya, Arumugam ;
Shunmugiah, Karutha Pandian .
JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS, 2021, 39 (13) :4594-4609
[8]   Traditional Herbal Medicines, Bioactive Metabolites, and Plant Products Against COVID-19: Update on Clinical Trials and Mechanism of Actions [J].
Alam, Safaet ;
Sarker, Md. Moklesur Rahman ;
Afrin, Sadia ;
Richi, Fahmida Tasnim ;
Zhao, Chao ;
Zhou, Jin-Rong ;
Mohamed, Isa Naina .
FRONTIERS IN PHARMACOLOGY, 2021, 12
[9]   In silicovirtual screening, characterization, docking and molecular dynamics studies of crucial SARS-CoV-2 proteins [J].
Alazmi, Meshari ;
Motwalli, Olaa .
JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS, 2021, 39 (17) :6761-6771
[10]   Severe Acute Respiratory Syndrome Coronavirus Nonstructural Proteins 3, 4, and 6 Induce Double-Membrane Vesicles [J].
Angelini, Megan M. ;
Akhlaghpour, Marzieh ;
Neuman, Benjamin W. ;
Buchmeier, Michael J. .
MBIO, 2013, 4 (04)