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Targeting ACLY efficiently inhibits SARS-CoV-2 replication
Authors:Terrence Tsz-Tai Yuen  Jasper Fuk-Woo Chan  Bingpeng Yan  Cynthia Cheuk-Ying Shum  Yuanchen Liu  Huiping Shuai  Yuxin Hou  Xiner Huang  Bingjie Hu  Yue Chai  Chaemin Yoon  Tianrenzheng Zhu  Huan Liu  Jialu Shi  Jinjin Zhang  Jian-Piao Cai  Anna Jinxia Zhang  Jie Zhou  Feifei Yin  Shuofeng Yuan  Bao-Zhong Zhang  Hin Chu
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, in vitro, and in vivo 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.
Keywords:COVID-19   metabolomics   ACLY   SARS-CoV-2   Delta   Omicron
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