Enisamium Inhibits SARS-CoV-2 RNA Synthesis

被引:5
作者
Elli, Stefano [1 ]
Bojkova, Denisa [2 ]
Bechtel, Marco [2 ]
Vial, Thomas [3 ]
Boltz, David [4 ]
Muzzio, Miguel [4 ]
Peng, Xinjian [4 ]
Sala, Federico [1 ]
Cosentino, Cesare [1 ]
Goy, Andrew [5 ]
Guerrini, Marco [1 ]
Mueller, Lutz [6 ]
Cinatl, Jindrich [2 ]
Margitich, Victor [5 ]
te Velthuis, Aartjan J. W. [3 ,7 ]
机构
[1] Ist Ric Chim & Biochim G Ronzoni, Via Giuseppe Colombo 81, I-20133 Milan, Italy
[2] Goethe Univ, Univ Hosp Frankfurt Main, Inst Med Virol, Paul Ehrlich Str 40, D-60596 Frankfurt, Germany
[3] Univ Cambridge, Addenbrookes Hosp, Dept Pathol, Div Virol, Hills Rd, Cambridge CB2 2QQ, England
[4] IIT Res Inst, 10 W 35th St, Chicago, IL 60616 USA
[5] Farmak Joint Stock Co, Kyrylivska St, UA-04080 Kiev, Ukraine
[6] Regenold GmbH, Zollinpl 4, D-79410 Badenweiler, Germany
[7] Princeton Univ, Lewis Thomas Lab, Dept Mol Biol, Princeton, NJ 08544 USA
基金
英国惠康基金;
关键词
COVID-19; SARS-CoV-2; molecular dynamics simulation; RNA polymerase; FAV00A; Amizon; POLYMERASE;
D O I
10.3390/biomedicines9091254
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pandemic SARS-CoV-2 causes a mild to severe respiratory disease called coronavirus disease 2019 (COVID-19). While control of the SARS-CoV-2 spread partly depends on vaccine-induced or naturally acquired protective herd immunity, antiviral strategies are still needed to manage COVID-19. Enisamium is an inhibitor of influenza A and B viruses in cell culture and clinically approved in countries of the Commonwealth of Independent States. In vitro, enisamium acts through metabolite VR17-04 and inhibits the activity of the influenza A virus RNA polymerase. Here we show that enisamium can inhibit coronavirus infections in NHBE and Caco-2 cells, and the activity of the SARS-CoV-2 RNA polymerase in vitro. Docking and molecular dynamics simulations provide insight into the mechanism of action and indicate that enisamium metabolite VR17-04 prevents GTP and UTP incorporation. Overall, these results suggest that enisamium is an inhibitor of SARS-CoV-2 RNA synthesis in vitro.
引用
收藏
页数:13
相关论文
共 31 条
[1]  
Beigel JH, 2020, NEW ENGL J MED, V383, P1813, DOI [10.1056/NEJMoa2007764, 10.1056/NEJMc2022236]
[2]   Aprotinin Inhibits SARS-CoV-2 Replication [J].
Bojkova, Denisa ;
Bechtel, Marco ;
McLaughlin, Katie-May ;
McGreig, Jake E. ;
Klann, Kevin ;
Bellinghausen, Carla ;
Rohde, Gernot ;
Jonigk, Danny ;
Braubach, Peter ;
Ciesek, Sandra ;
Muench, Christian ;
Wass, Mark N. ;
Michaelis, Martin ;
Cinatl, Jindrich .
CELLS, 2020, 9 (11)
[3]   Proteomics of SARS-CoV-2-infected host cells reveals therapy targets [J].
Bojkova, Denisa ;
Klann, Kevin ;
Koch, Benjamin ;
Widera, Marek ;
Krause, David ;
Ciesek, Sandra ;
Cinatl, Jindrich ;
Muench, Christian .
NATURE, 2020, 583 (7816) :469-+
[4]  
Boltz David, 2018, Antiviral Chemistry & Chemotherapy, V26, DOI 10.1177/2040206618811416
[5]   The Amber biomolecular simulation programs [J].
Case, DA ;
Cheatham, TE ;
Darden, T ;
Gohlke, H ;
Luo, R ;
Merz, KM ;
Onufriev, A ;
Simmerling, C ;
Wang, B ;
Woods, RJ .
JOURNAL OF COMPUTATIONAL CHEMISTRY, 2005, 26 (16) :1668-1688
[6]   Structural Basis for Helicase-Polymerase Coupling in the SARS-CoV-2 Replication-Transcription Complex [J].
Chen, James ;
Malone, Brandon ;
Llewellyn, Eliza ;
Grasso, Michael ;
Shelton, Patrick M. M. ;
Olinares, Paul Dominic B. ;
Maruthi, Kashyap ;
Eng, Edward T. ;
Vatandaslar, Hasan ;
Chait, Brian T. ;
Kapoor, Tarun M. ;
Darst, Seth A. ;
Campbell, Elizabeth A. .
CELL, 2020, 182 (06) :1560-+
[7]   Therapeutically administered ribonucleoside analogue MK-4482/EIDD-2801 blocks SARS-CoV-2 transmission in ferrets [J].
Cox, Robert M. ;
Wolf, Josef D. ;
Plemper, Richard K. .
NATURE MICROBIOLOGY, 2021, 6 (01) :11-+
[8]  
Frisch M.J., 2016, Gaussian 16, Revision C.01
[9]   ITERATIVE PARTIAL EQUALIZATION OF ORBITAL ELECTRONEGATIVITY - A RAPID ACCESS TO ATOMIC CHARGES [J].
GASTEIGER, J ;
MARSILI, M .
TETRAHEDRON, 1980, 36 (22) :3219-3228
[10]   The mechanism of resistance to favipiravir in influenza [J].
Goldhill, Daniel H. ;
te Velthuis, Aartjan J. W. ;
Fletcher, Robert A. ;
Langat, Pinky ;
Zambon, Maria ;
Lackenby, Angie ;
Barclay, Wendy S. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2018, 115 (45) :11613-11618