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Research Advances on the Role of Lipids in the Life Cycle of Human Coronaviruses.

作者信息

Ding Cuiling, Chen Yibo, Miao Gen, Qi Zhongtian

机构信息

Department of Microbiology, Faculty of Naval Medicine, Naval Medical University, Shanghai 200433, China.

Department of Nutrition and Food Hygiene, Faculty of Naval Medicine, Naval Medical University, Shanghai 200433, China.

出版信息

Microorganisms. 2023 Dec 28;12(1):63. doi: 10.3390/microorganisms12010063.


DOI:10.3390/microorganisms12010063
PMID:38257890
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10820681/
Abstract

Coronaviruses (CoVs) are emerging pathogens with a significant potential to cause life-threatening harm to human health. Since the beginning of the 21st century, three highly pathogenic and transmissible human CoVs have emerged, triggering epidemics and posing major threats to global public health. CoVs are enveloped viruses encased in a lipid bilayer. As fundamental components of cells, lipids can play an integral role in many physiological processes, which have been reported to play important roles in the life cycle of CoVs, including viral entry, uncoating, replication, assembly, and release. Therefore, research on the role of lipids in the CoV life cycle can provide a basis for a better understanding of the infection mechanism of CoVs and provide lipid targets for the development of new antiviral strategies. In this review, research advances on the role of lipids in different stages of viral infection and the possible targets of lipids that interfere with the viral life cycle are discussed.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d7/10820681/c8989a7e8d89/microorganisms-12-00063-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d7/10820681/c764fe9d44ec/microorganisms-12-00063-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d7/10820681/c8989a7e8d89/microorganisms-12-00063-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d7/10820681/c764fe9d44ec/microorganisms-12-00063-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d7/10820681/c8989a7e8d89/microorganisms-12-00063-g002.jpg

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引用本文的文献

[1]
Direct lipid interactions control SARS-CoV-2 M protein conformational dynamics and virus assembly.

bioRxiv. 2024-11-5

[2]
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[3]
Design and Application of Biosafe Coronavirus Engineering Systems without Virulence.

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本文引用的文献

[1]
Inhibition of the SREBP pathway prevents SARS-CoV-2 replication and inflammasome activation.

Life Sci Alliance. 2023-11

[2]
SARS-CoV-2 Envelope Protein Forms Clustered Pentamers in Lipid Bilayers.

Biochemistry. 2022-11-1

[3]
Lipid Raft Integrity and Cellular Cholesterol Homeostasis Are Critical for SARS-CoV-2 Entry into Cells.

Nutrients. 2022-8-19

[4]
The double-membrane vesicle (DMV): a virus-induced organelle dedicated to the replication of SARS-CoV-2 and other positive-sense single-stranded RNA viruses.

Cell Mol Life Sci. 2022-7-16

[5]
COVID-19 and Lipid Disorders.

Horm Metab Res. 2022-8

[6]
Antiviral efficacy of selective estrogen receptor modulators against SARS-CoV-2 infection in vitro and in vivo reveals bazedoxifene acetate as an entry inhibitor.

J Med Virol. 2022-10

[7]
Palmitoylethanolamide (PEA) Inhibits SARS-CoV-2 Entry by Interacting with S Protein and ACE-2 Receptor.

Viruses. 2022-5-17

[8]
Coronavirus Infection and Cholesterol Metabolism.

Front Immunol. 2022

[9]
Lipid rafts as viral entry routes and immune platforms: A double-edged sword in SARS-CoV-2 infection?

Biochim Biophys Acta Mol Cell Biol Lipids. 2022-6

[10]
Elucidation of SARS-Cov-2 Budding Mechanisms through Molecular Dynamics Simulations of M and E Protein Complexes.

J Phys Chem Lett. 2021-12-30

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