Literature DB >> 33396288

A Novel Ebola Virus VP40 Matrix Protein-Based Screening for Identification of Novel Candidate Medical Countermeasures.

Ryan P Bennett1, Courtney L Finch2, Elena N Postnikova2, Ryan A Stewart1, Yingyun Cai2, Shuiqing Yu2, Janie Liang2, Julie Dyall2, Jason D Salter1, Harold C Smith1, Jens H Kuhn2.   

Abstract

Filoviruses, such as Ebola virus and Marburg virus, are of significant human health concern. From 2013 to 2016, Ebola virus caused 11,323 fatalities in Western Africa. Since 2018, two Ebola virus disease outbreaks in the Democratic Republic of the Congo resulted in 2354 fatalities. Although there is progress in medical countermeasure (MCM) development (in particular, vaccines and antibody-based therapeutics), the need for efficacious small-molecule therapeutics remains unmet. Here we describe a novel high-throughput screening assay to identify inhibitors of Ebola virus VP40 matrix protein association with viral particle assembly sites on the interior of the host cell plasma membrane. Using this assay, we screened nearly 3000 small molecules and identified several molecules with the desired inhibitory properties. In secondary assays, one identified compound, sangivamycin, inhibited not only Ebola viral infectivity but also that of other viruses. This finding indicates that it is possible for this new VP40-based screening method to identify highly potent MCMs against Ebola virus and its relatives.

Entities:  

Keywords:  Ebola virus; Filoviridae; MCM; Marburg virus; VP40; broad spectrum; filovirus; sangivamycin

Year:  2020        PMID: 33396288      PMCID: PMC7824103          DOI: 10.3390/v13010052

Source DB:  PubMed          Journal:  Viruses        ISSN: 1999-4915            Impact factor:   5.048


  74 in total

1.  Emergence of Ebola Virus Escape Variants in Infected Nonhuman Primates Treated with the MB-003 Antibody Cocktail.

Authors:  Jeffrey R Kugelman; Johanny Kugelman-Tonos; Jason T Ladner; James Pettit; Carolyn M Keeton; Elyse R Nagle; Karla Y Garcia; Jeffrey W Froude; Ana I Kuehne; Jens H Kuhn; Sina Bavari; Larry Zeitlin; John M Dye; Gene G Olinger; Mariano Sanchez-Lockhart; Gustavo F Palacios
Journal:  Cell Rep       Date:  2015-09-10       Impact factor: 9.423

2.  Both matrix proteins of Ebola virus contribute to the regulation of viral genome replication and transcription.

Authors:  T Hoenen; S Jung; A Herwig; A Groseth; S Becker
Journal:  Virology       Date:  2010-05-04       Impact factor: 3.616

3.  Vesicular release of ebola virus matrix protein VP40.

Authors:  J Timmins; S Scianimanico; G Schoehn; W Weissenhorn
Journal:  Virology       Date:  2001-04-25       Impact factor: 3.616

4.  Structural rearrangement of ebola virus VP40 begets multiple functions in the virus life cycle.

Authors:  Zachary A Bornholdt; Takeshi Noda; Dafna M Abelson; Peter Halfmann; Malcolm R Wood; Yoshihiro Kawaoka; Erica Ollmann Saphire
Journal:  Cell       Date:  2013-08-15       Impact factor: 41.582

5.  The L-VP35 and L-L interaction domains reside in the amino terminus of the Ebola virus L protein and are potential targets for antivirals.

Authors:  Martina Trunschke; Dominik Conrad; Sven Enterlein; Judith Olejnik; Kristina Brauburger; Elke Mühlberger
Journal:  Virology       Date:  2013-04-11       Impact factor: 3.616

6.  A new biological role of sangivamycin; inhibition of protein kinases.

Authors:  H Osada; T Sonoda; K Tsunoda; K Isono
Journal:  J Antibiot (Tokyo)       Date:  1989-01       Impact factor: 2.649

7.  The matrix protein VP40 from Ebola virus octamerizes into pore-like structures with specific RNA binding properties.

Authors:  F Xavier Gomis-Rüth; Andréa Dessen; Joanna Timmins; Andreas Bracher; Larissa Kolesnikowa; Stephan Becker; Hans Dieter Klenk; Winfried Weissenhorn
Journal:  Structure       Date:  2003-04       Impact factor: 5.006

8.  Assembly of Ebola virus matrix protein VP40 is regulated by latch-like properties of N and C terminal tails.

Authors:  Leslie P Silva; Michael Vanzile; Sina Bavari; J M Javad Aman; David C Schriemer
Journal:  PLoS One       Date:  2012-07-05       Impact factor: 3.240

9.  Toremifene interacts with and destabilizes the Ebola virus glycoprotein.

Authors:  Yuguang Zhao; Jingshan Ren; Karl Harlos; Daniel M Jones; Antra Zeltina; Thomas A Bowden; Sergi Padilla-Parra; Elizabeth E Fry; David I Stuart
Journal:  Nature       Date:  2016-06-29       Impact factor: 49.962

10.  Sangivamycin and its derivatives inhibit Haspin-Histone H3-survivin signaling and induce pancreatic cancer cell death.

Authors:  Ligia I Bastea; Laeticia M A Hollant; Heike R Döppler; Elizabeth M Reid; Peter Storz
Journal:  Sci Rep       Date:  2019-11-12       Impact factor: 4.379

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  3 in total

1.  Sangivamycin is highly effective against SARS-CoV-2 in vitro and has favorable drug properties.

Authors:  Ryan P Bennett; Elena N Postnikova; Brett P Eaton; Yingyun Cai; Shuiqing Yu; Charles O Smith; Janie Liang; Huanying Zhou; Gregory A Kocher; Michael J Murphy; Harold C Smith; Jens H Kuhn
Journal:  JCI Insight       Date:  2022-01-11

2.  Generation of Reporter-Expressing New World Arenaviruses: A Systematic Comparison.

Authors:  Lucie Fénéant; Anne Leske; Karla Günther; Allison Groseth
Journal:  Viruses       Date:  2022-07-18       Impact factor: 5.818

3.  Formulation, Stability, Pharmacokinetic, and Modeling Studies for Tests of Synergistic Combinations of Orally Available Approved Drugs against Ebola Virus In Vivo.

Authors:  Courtney L Finch; Julie Dyall; Shuang Xu; Elizabeth A Nelson; Elena Postnikova; Janie Y Liang; Huanying Zhou; Lisa Evans DeWald; Craig J Thomas; Amy Wang; Xin Xu; Emma Hughes; Patrick J Morris; Jon C Mirsalis; Linh H Nguyen; Maria P Arolfo; Bryan Koci; Michael R Holbrook; Lisa E Hensley; Peter B Jahrling; Connie Schmaljohn; Lisa M Johansen; Gene G Olinger; Joshua T Schiffer; Judith M White
Journal:  Microorganisms       Date:  2021-03-10
  3 in total

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