Ginkgolic Acid Inhibits Coronavirus Strain 229E Infection of Human Epithelial Lung Cells

被引:9
|
作者
Bhutta, Maimoona S. [1 ]
Sausen, Daniel G. [1 ]
Gallo, Elisa S. [2 ]
Dahari, Harel [3 ]
Doncel, Gustavo F. [4 ]
Borenstein, Ronen [1 ,3 ]
机构
[1] Eastern Virginia Med Sch, Dept Microbiol & Mol Cell Biol, Norfolk, VA 23507 USA
[2] Rush Univ, Med Ctr Pinnacle Dermatol, Barrington, IL 60010 USA
[3] Loyola Univ Chicago, Stritch Sch Med, Dept Med, Program Expt & Theoret Modeling,Div Hepatol, Maywood, IL 60153 USA
[4] Eastern Virginia Med Sch, Dept Obstet & Gynecol, CONRAD, Norfolk, VA 23507 USA
基金
美国国家卫生研究院;
关键词
ginkgolic acid; coronavirus; antiviral; fusion inhibitor; HCoV-229E; BILOBA; PROTEIN; CANCER; AMPK;
D O I
10.3390/ph14100980
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Since December 2019, the COVID-19 pandemic has affected more than 200 million individuals around the globe and caused millions of deaths. Although there are now multiple vaccines for SARS-CoV-2, their efficacy may be limited by current and future viral mutations. Therefore, effective antiviral compounds are an essential component to win the battle against the family of coronaviruses. Ginkgolic Acid (GA) is a pan-antiviral molecule with proven effective in vitro and in vivo activity. We previously demonstrated that GA inhibits Herpes Simplex Virus 1 (HSV-1) by disrupting viral structure, blocking fusion, and inhibiting viral protein synthesis. Additionally, we reported that GA displays broad-spectrum fusion inhibition encompassing all three classes of fusion proteins, including those of HIV, Ebola, influenza A, and Epstein Barr virus. Here, we report that GA exhibited potent antiviral activity against Human Coronavirus strain 229E (HCoV-229E) infection of human epithelial lung cells (MRC-5). GA significantly reduced progeny virus production, expression of viral proteins, and cytopathic effects (CPE). Furthermore, GA significantly inhibited HCoV-229E even when added post-infection. In light of our findings and the similarities of this family of viruses, GA holds promising potential as an effective antiviral treatment for SARS-CoV-2.
引用
收藏
页数:11
相关论文
共 50 条
  • [1] Infection of human alveolar macrophages by human coronavirus strain 229E
    Funk, C. Joel
    Wang, Jieru
    Ito, Yoko
    Travanty, Emily A.
    Voelker, Dennis R.
    Holmes, Kathryn V.
    Mason, Robert J.
    JOURNAL OF GENERAL VIROLOGY, 2012, 93 : 494 - 503
  • [2] GENOME OF HUMAN CORONAVIRUS STRAIN 229E
    MACNAUGHTON, MR
    MADGE, MH
    JOURNAL OF GENERAL VIROLOGY, 1978, 39 (JUN): : 497 - 504
  • [3] Suppression of Human Coronavirus 229E Infection in Lung Fibroblast Cells via RNA Interference
    Aliabadi, Hamidreza Montazeri
    Totonchy, Jennifer
    Mahdipoor, Parvin
    Parang, Keykavous
    Uludag, Hasan
    FRONTIERS IN NANOTECHNOLOGY, 2021, 3
  • [4] ESTABLISHMENT AND MAINTENANCE OF A PERSISTENT INFECTION OF L132 CELLS BY HUMAN CORONAVIRUS STRAIN 229E
    CHALONERLARSSON, G
    JOHNSONLUSSENBURG, CM
    ARCHIVES OF VIROLOGY, 1981, 69 (02) : 117 - 129
  • [5] THE DISTRIBUTION OF HUMAN CORONAVIRUS STRAIN 229E ON THE SURFACE OF HUMAN-DIPLOID CELLS
    PATTERSON, S
    MACNAUGHTON, MR
    JOURNAL OF GENERAL VIROLOGY, 1981, 53 (APR): : 267 - 273
  • [6] Spike-Independent Infection of Human Coronavirus 229E in Bat Cells
    Mah, Marcus G.
    Linster, Martin
    Low, Dolyce H. W.
    Zhuang, Yan
    Jayakumar, Jayanthi
    Samsudin, Firdaus
    Wong, Foong Ying
    Bond, Peter J.
    Mendenhall, Ian H.
    Su, Yvonne C. F.
    Smith, Gavin J. D.
    MICROBIOLOGY SPECTRUM, 2023, 11 (03):
  • [7] Activation of human monocytes after infection by human coronavirus 229E
    Desforges, Marc
    Miletti, Tina C.
    Gagnon, Mylene
    Talbot, Pierre J.
    VIRUS RESEARCH, 2007, 130 (1-2) : 228 - 240
  • [8] ISOLATION AND MORPHOLOGY OF INTERNAL COMPONENT OF HUMAN CORONAVIRUS, STRAIN 229E
    KENNEDY, DA
    JOHNSONLUSSENBURG, CM
    INTERVIROLOGY, 1976, 6 (4-5) : 197 - 206
  • [9] Investigation of the impact of chemical inhibitors on different epithelial cells infected with the human coronavirus 229E
    Mayr-Buro, C.
    Geradts, A. S.
    Kracht, M.
    NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 2022, 395 (SUPPL 1) : S9 - S10
  • [10] Delayed immunological reaction of Human Microvascular Lung Endothelium in response to Human Coronavirus 229E infection
    Szewczyk, R.
    Gawrysiak, M.
    Gajewski, A.
    Chalubinski, M.
    EUROPEAN RESPIRATORY JOURNAL, 2022, 60