TMPRSS2 and RNA-Dependent RNA Polymerase Are Effective Targets of Therapeutic Intervention for Treatment of COVID-19 Caused by SARS-CoV-2 Variants (B.1.1.7 and B.1.351)

被引:18
|
作者
Lee, Jihye [1 ]
Lee, JinAh [1 ]
Kim, Hyeon Ju [1 ]
Ko, Meehyun [1 ]
Jee, Youngmee [2 ]
Kim, Seungtaek [1 ]
机构
[1] Inst Pasteur Korea, Zoonot Virus Lab, Seongnam, South Korea
[2] Inst Pasteur Korea, CEO Off, Seongnam, South Korea
来源
MICROBIOLOGY SPECTRUM | 2021年 / 9卷 / 01期
基金
新加坡国家研究基金会;
关键词
COVID-19; RNA-dependent RNA polymerase; SARS-CoV-2; TMPRSS2; variant; IDENTIFICATION; MUTATIONS; VIRUS;
D O I
10.1128/Spectrum.00472-21
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a causative agent of the coronavirus disease 2019 (COVID-19) pandemic, and the development of therapeutic interventions is urgently needed. So far, monoclonal antibodies and drug repositioning are the main methods for drug development, and this effort was partially successful. Since the beginning of the COVID-19 pandemic, the emergence of SARS-CoV-2 variants has been reported in many parts of the world, and the main concern is whether the current vaccines and therapeutics are still effective against these variant viruses. Viral entry and viral RNA-dependent RNA polymerase (RdRp) are the main targets of current drug development; therefore, the inhibitory effects of transmembrane serine protease 2 (TMPRSS2) and RdRp inhibitors were compared among the early SARS-CoV-2 isolate (lineage A) and the two recent variants (lineage 8.1.1.7 and lineage 8.1351) identified in the United Kingdom and South Africa, respectively. Our in vitro analysis of viral replication showed that the drugs targeting TMPRSS2 and RdRp are equally effective against the two variants of concern. IMPORTANCE The COVID-19 pandemic is causing unprecedented global problems in both public health and human society. While some vaccines and monoclonal antibodies were successfully developed very quickly and are currently being used, numerous variants of the causative SARS-CoV-2 are emerging and threatening the efficacy of vaccines and monoclonal antibodies. In order to respond to this challenge, we assessed antiviral efficacy of small-molecule inhibitors that are being developed for treatment of COVID-19 and found that they are still very effective against the SARS-CoV-2 variants. Since most small-molecule inhibitors target viral or host factors other than the mutated sequence of the viral spike protein, they are expected to be potent control measures against the COVID-19 pandemic.
引用
收藏
页码:1 / 7
页数:7
相关论文
共 50 条
  • [41] Increased risk of hospitalisation and intensive care admission associated with reported cases of SARS-CoV-2 variants B.1.1.7 and B.1.351 in Norway, December 2020-May 2021
    Veneti, Lamprini
    Seppala, Elina
    Storm, Margrethe Larsdatter
    Salamanca, Beatriz Valcarcel
    Buanes, Eirik Alnes
    Aasand, Nina
    Naseer, Umaer
    Bragstad, Karoline
    Hungnes, Olav
    Boas, Hakon
    Kvale, Reidar
    Golestani, Karan
    Feruglio, Siri
    Vold, Line
    Nygard, Karin
    Whittaker, Robert
    PLOS ONE, 2021, 16 (10):
  • [42] SARS-CoV-2 B.1.1.7 reinfection after previous COVID-19 in two immunocompetent Italian patients
    Novazzi, Federica
    Baj, Andreina
    Genoni, Angelo
    Spezia, Pietro G.
    Colombo, Alberto
    Cassani, Gianluca
    Zago, Cristian
    Pasciuta, Renee
    Della Gasperina, Daniela
    Ageno, Walter
    Severgnini, Paolo
    Dentali, Francesco
    Focosi, Daniele
    Maggi, Fabrizio
    JOURNAL OF MEDICAL VIROLOGY, 2021, 93 (09) : 5648 - 5649
  • [43] Increased Residential Clustering of COVID-19 Cases Associated With SARS-CoV-2 Variant of Concern B.1.1.7
    Flannagan, Joe
    Twohig, Katherine A.
    Carter, Emma
    Chudasama, Dimple Y.
    Lamagni, Theresa
    Dabrera, Gavin
    EPIDEMIOLOGY, 2022, 33 (04) : 465 - 469
  • [44] The Binding of Remdesivir to SARS-CoV-2 RNA-Dependent RNA Polymerase May Pave The Way Towards the Design of Potential Drugs for COVID-19 Treatment
    Agoni, Clement
    Soliman, Mahmoud E. S.
    CURRENT PHARMACEUTICAL BIOTECHNOLOGY, 2021, 22 (11) : 1520 - 1537
  • [45] Changing Features of COVID-19: Characteristics of Infections with the SARS-CoV-2 Delta (B.1.617.2) and Alpha (B.1.1.7) Variants in Southern Italy
    Loconsole, Daniela
    Centrone, Francesca
    Morcavallo, Caterina
    Campanella, Silvia
    Accogli, Marisa
    Sallustio, Anna
    Peccarisi, Davide
    Stufano, Angela
    Lovreglio, Piero
    Chironna, Maria
    VACCINES, 2021, 9 (11)
  • [46] Immunoinformatics-Based Identification of B and T Cell Epitopes in RNA-Dependent RNA Polymerase of SARS-CoV-2
    Mir, Shabir Ahmad
    Alaidarous, Mohammed
    Alshehri, Bader
    Bin Dukhyil, Abdul Aziz
    Banawas, Saeed
    Madkhali, Yahya
    Alsagaby, Suliman A.
    Al Othaim, Ayoub
    VACCINES, 2022, 10 (10)
  • [47] Virtual Combinatorial Library Screening of Quinadoline B Derivatives against SARS-CoV-2 RNA-Dependent RNA Polymerase
    Brogi, Simone
    Quimque, Mark Tristan
    Notarte, Kin Israel
    Africa, Jeremiah Gabriel
    Hernandez, Jenina Beatriz
    Tan, Sophia Morgan
    Calderone, Vincenzo
    Macabeo, Allan Patrick
    COMPUTATION, 2022, 10 (01)
  • [48] Immunoinformatics Identification of B- and T-Cell Epitopes in the RNA-Dependent RNA Polymerase of SARS-CoV-2
    Yashvardhini, Niti
    Kumar, Amit
    Jha, Deepak Kumar
    CANADIAN JOURNAL OF INFECTIOUS DISEASES & MEDICAL MICROBIOLOGY, 2021, 2021
  • [49] Fe-S cofactors in the SARS-CoV-2 RNA-dependent RNA polymerase are potential antiviral targets
    Maio, Nunziata
    Lafont, Bernard A. P.
    Sil, Debangsu
    Li, Yan
    Bollinger, J. Martin, Jr.
    Krebs, Carsten
    Pierson, Theodore C.
    Linehan, W. Marston
    Rouault, Tracey A.
    SCIENCE, 2021, 373 (6551) : 236 - +
  • [50] Severity of infection with the SARS-CoV-2 B.1.1.7 lineage among hospitalized COVID-19 patients in Belgium
    Van Goethem, Nina
    Vandromme, Mathil
    Van Oyen, Herman
    Haarhuis, Freek
    Brondeel, Ruben
    Catteau, Lucy
    Andre, Emmanuel
    Cuypers, Lize
    Blot, Koen
    Serrien, Ben
    PLOS ONE, 2022, 17 (06):