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靶向 ACLY 能有效抑制 SARS-CoV-2 复制。

Targeting ACLY efficiently inhibits SARS-CoV-2 replication.

机构信息

State Key Laboratory of Emerging Infectious Diseases, Department of Microbiology, and Carol Yu Centre for Infection, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, People's Republic of China.

Department of Clinical Microbiology and Infection Control, The University of Hong Kong-Shenzhen Hospital, Shenzhen, Guangdong, People's Republic of China.

出版信息

Int J Biol Sci. 2022 Jul 11;18(12):4714-4730. doi: 10.7150/ijbs.72709. eCollection 2022.

Abstract

The Coronavirus Disease 2019 (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the biggest public health challenge the world has witnessed in the past decades. SARS-CoV-2 undergoes constant mutations and new variants of concerns (VOCs) with altered transmissibility, virulence, and/or susceptibility to vaccines and therapeutics continue to emerge. Detailed analysis of host factors involved in virus replication may help to identify novel treatment targets. In this study, we dissected the metabolome derived from COVID-19 patients to identify key host factors that are required for efficient SARS-CoV-2 replication. Through a series of metabolomic analyses, , and investigations, we identified ATP citrate lyase (ACLY) as a novel host factor required for efficient replication of SARS-CoV-2 wild-type and variants, including Omicron. ACLY should be further explored as a novel intervention target for COVID-19.

摘要

由严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)引起的 2019 年冠状病毒病(COVID-19)大流行是过去几十年来全球面临的最大公共卫生挑战。SARS-CoV-2 不断发生突变,新出现的关切变异株(VOCs)具有改变的传染性、毒力和/或对疫苗和疗法的敏感性。详细分析宿主中参与病毒复制的因素可能有助于确定新的治疗靶点。在这项研究中,我们剖析了 COVID-19 患者的代谢组,以确定有效复制 SARS-CoV-2 所需的关键宿主因素。通过一系列代谢组学分析、实验验证和机制研究,我们确定三羧酸循环酶(ACLY)是有效复制 SARS-CoV-2 野生型和变体(包括奥密克戎)所必需的新型宿主因子。ACLY 应进一步作为 COVID-19 的新型干预靶点进行探索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5b9/9305265/4dee160f1da6/ijbsv18p4714g001.jpg

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