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Article: Targeting ACLY efficiently inhibits SARS-CoV-2 replication

TitleTargeting ACLY efficiently inhibits SARS-CoV-2 replication
Authors
KeywordsACLY
COVID-19
Delta
metabolomics
Omicron
SARS-CoV-2
Issue Date2022
Citation
International Journal of Biological Sciences, 2022, v. 18, n. 12, p. 4714-4730 How to Cite?
AbstractThe 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.
Persistent Identifierhttp://hdl.handle.net/10722/315206
ISSN
2021 Impact Factor: 10.750
2020 SCImago Journal Rankings: 1.647
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorYuen, Terrence Tsz Tai-
dc.contributor.authorChan, Jasper Fuk Woo-
dc.contributor.authorYan, Bingpeng-
dc.contributor.authorShum, Cynthia Cheuk Ying-
dc.contributor.authorLiu, Yuanchen-
dc.contributor.authorShuai, Huiping-
dc.contributor.authorHou, Yuxin-
dc.contributor.authorHuang, Xiner-
dc.contributor.authorHu, Bingjie-
dc.contributor.authorChai, Yue-
dc.contributor.authorYoon, Chaemin-
dc.contributor.authorZhu, Tianrenzheng-
dc.contributor.authorLiu, Huan-
dc.contributor.authorShi, Jialu-
dc.contributor.authorZhang, Jinjin-
dc.contributor.authorCai, Jian Piao-
dc.contributor.authorZhang, Anna Jinxia-
dc.contributor.authorZhou, Jie-
dc.contributor.authorYin, Feifei-
dc.contributor.authorYuan, Shuofeng-
dc.contributor.authorZhang, Bao Zhong-
dc.contributor.authorChu, Hin-
dc.date.accessioned2022-08-05T10:18:02Z-
dc.date.available2022-08-05T10:18:02Z-
dc.date.issued2022-
dc.identifier.citationInternational Journal of Biological Sciences, 2022, v. 18, n. 12, p. 4714-4730-
dc.identifier.issn1449-2288-
dc.identifier.urihttp://hdl.handle.net/10722/315206-
dc.description.abstractThe 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.-
dc.languageeng-
dc.relation.ispartofInternational Journal of Biological Sciences-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectACLY-
dc.subjectCOVID-19-
dc.subjectDelta-
dc.subjectmetabolomics-
dc.subjectOmicron-
dc.subjectSARS-CoV-2-
dc.titleTargeting ACLY efficiently inhibits SARS-CoV-2 replication-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.7150/ijbs.72709-
dc.identifier.pmid35874959-
dc.identifier.pmcidPMC9305265-
dc.identifier.scopuseid_2-s2.0-85134152870-
dc.identifier.volume18-
dc.identifier.issue12-
dc.identifier.spage4714-
dc.identifier.epage4730-
dc.identifier.isiWOS:000828439300021-

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