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Abelson Kinase Inhibitors Are Potent Inhibitors of Severe Acute Respiratory Syndrome Coronavirus and Middle East Respiratory Syndrome Coronavirus Fusion.

作者信息

Coleman Christopher M, Sisk Jeanne M, Mingo Rebecca M, Nelson Elizabeth A, White Judith M, Frieman Matthew B

机构信息

Department of Microbiology and Immunology, University of Maryland, Baltimore, Maryland, USA.

Department of Cell Biology, University of Virginia, Charlottesville, Virginia, USA.

出版信息

J Virol. 2016 Sep 12;90(19):8924-33. doi: 10.1128/JVI.01429-16. Print 2016 Oct 1.


DOI:10.1128/JVI.01429-16
PMID:27466418
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5021412/
Abstract

UNLABELLED: The highly pathogenic severe acute respiratory syndrome coronavirus (SARS-CoV) and Middle East respiratory syndrome coronavirus (MERS-CoV) cause significant morbidity and morality. There is currently no approved therapeutic for highly pathogenic coronaviruses, even as MERS-CoV is spreading throughout the Middle East. We previously screened a library of FDA-approved drugs for inhibitors of coronavirus replication in which we identified Abelson (Abl) kinase inhibitors, including the anticancer drug imatinib, as inhibitors of both SARS-CoV and MERS-CoV in vitro Here we show that the anti-CoV activity of imatinib occurs at the early stages of infection, after internalization and endosomal trafficking, by inhibiting fusion of the virions at the endosomal membrane. We specifically identified the imatinib target, Abelson tyrosine-protein kinase 2 (Abl2), as required for efficient SARS-CoV and MERS-CoV replication in vitro These data demonstrate that specific approved drugs can be characterized in vitro for their anticoronavirus activity and used to identify host proteins required for coronavirus replication. This type of study is an important step in the repurposing of approved drugs for treatment of emerging coronaviruses. IMPORTANCE: Both SARS-CoV and MERS-CoV are zoonotic infections, with bats as the primary source. The 2003 SARS-CoV outbreak began in Guangdong Province in China and spread to humans via civet cats and raccoon dogs in the wet markets before spreading to 37 countries. The virus caused 8,096 confirmed cases of SARS and 774 deaths (a case fatality rate of ∼10%). The MERS-CoV outbreak began in Saudi Arabia and has spread to 27 countries. MERS-CoV is believed to have emerged from bats and passed into humans via camels. The ongoing outbreak of MERS-CoV has resulted in 1,791 cases of MERS and 640 deaths (a case fatality rate of 36%). The emergence of SARS-CoV and MERS-CoV provides evidence that coronaviruses are currently spreading from zoonotic sources and can be highly pathogenic, causing serious morbidity and mortality in humans. Treatment of SARS-CoV and MERS-CoV infection is limited to providing supportive therapy consistent with any serious lung disease, as no specific drugs have been approved as therapeutics. Highly pathogenic coronaviruses are rare and appear to emerge and disappear within just a few years. Currently, MERS-CoV is still spreading, as new infections continue to be reported. The outbreaks of SARS-CoV and MERS-CoV and the continuing diagnosis of new MERS cases highlight the need for finding therapeutics for these diseases and potential future coronavirus outbreaks. Screening FDA-approved drugs streamlines the pipeline for this process, as these drugs have already been tested for safety in humans.

摘要

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[1]
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本文引用的文献

[1]
The Emerging Role of ABL Kinases in Solid Tumors.

Trends Cancer. 2015-10-1

[2]
Severe Acute Respiratory Syndrome Coronavirus ORF7a Inhibits Bone Marrow Stromal Antigen 2 Virion Tethering through a Novel Mechanism of Glycosylation Interference.

J Virol. 2015-12

[3]
Growth and Quantification of MERS-CoV Infection.

Curr Protoc Microbiol. 2015-5-1

[4]
Identification of 53 compounds that block Ebola virus-like particle entry via a repurposing screen of approved drugs.

Emerg Microbes Infect. 2014-12

[5]
Coronaviruses: an overview of their replication and pathogenesis.

Methods Mol Biol. 2015

[6]
Safety and efficacy of imatinib in CML over a period of 10 years: data from the randomized CML-study IV.

Leukemia. 2015-2-13

[7]
Ebola virus and severe acute respiratory syndrome coronavirus display late cell entry kinetics: evidence that transport to NPC1+ endolysosomes is a rate-defining step.

J Virol. 2015-3

[8]
Coronavirus cell entry occurs through the endo-/lysosomal pathway in a proteolysis-dependent manner.

PLoS Pathog. 2014-11-6

[9]
Repurposing of clinically developed drugs for treatment of Middle East respiratory syndrome coronavirus infection.

Antimicrob Agents Chemother. 2014-8

[10]
Proteolytic activation of the SARS-coronavirus spike protein: cutting enzymes at the cutting edge of antiviral research.

Antiviral Res. 2013-10-8

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