Emerging Viruses and Antiviral Drugs 2.0

A special issue of Microorganisms (ISSN 2076-2607). This special issue belongs to the section "Virology".

Deadline for manuscript submissions: closed (31 March 2024) | Viewed by 1516

Special Issue Editors


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Guest Editor
Department of Quantitative Biosciences, Merck, Boston, MA, USA
Interests: antiviral drug discovery; phenotypic drug discovery; HCI
Special Issues, Collections and Topics in MDPI journals

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Guest Editor
Department of Biotechnology, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA), 28040 Madrid, Spain
Interests: virus; arbovirus; flavivirus; dengue; West Nile; Zika; zoonoses; lipid; virus–host interaction; sphingolipids; fatty acids; metabolism; antivirals; vaccines
Special Issues, Collections and Topics in MDPI journals

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Guest Editor
CSO, Co-founder of Healion Bio, Frederick, MD, USA
Interests: virology; oncology; drug discovery; drug development

Special Issue Information

Dear Colleagues,

Emerging viruses are a very broad category that includes not only newly discovered viruses but also re-emerging variants of known viruses. These viruses continue to cause mass disruption by creating constant threat to public health. In the last 20 years, we have observed a variety of viral outbreaks, such as severe acute respiratory symptom (SARS), H1N1 influenza, Ebola virus, Middle East respiratory syndrome coronavirus (MERS-CoV), Rift Valley fever, Crimean Congo hemorrhagic fever, Nipah and Hendra viruses, severe fever with thrombocytopenia syndrome virus (SFTSV), yellow fever virus (YFV), Zika virus, and the ongoing SARS-CoV-2. The globalization of the economies and quick-paced traveling patterns of human populations, combined with climate change, are creating ample opportunities for mass spread of viral infections. The multiple surges of SARS-CoV-2 variants have quickly exposed the challenges and limitations of vaccines and various antiviral treatments. For example, SARS-CoV-2 virus transmission has proven difficult to manage with current vaccines and therapeutic approaches. There is a strong need to position immune modulating modalities and other novel antivirals to suppress viral transmission and infection by inhibiting cellular pathways essential for viral infection.  The development of broad-spectrum antiviral drugs can provide an additional level of defense while specific antivirals are being developed. This approach has shown some indication of success against SARS-CoV-2 and may be appropriate to be implemented for future emerging viruses. This Special Issue, “Emerging Viruses and Antiviral Drugs”, focuses on various antiviral approaches to manage emerging and re-emerging viruses and will include antiviral drug discovery, discovery of the mechanism of actions, new targets, and upcoming and established technologies used for discovery and development of antiviral drugs.

Dr. Veronica Soloveva
Dr. Miguel A. Martín-Acebes
Dr. Sina Bavari
Guest Editors

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Keywords

  • emerging viruses
  • antiviral therapies
  • antiviral drugs
  • drug discovery and development
  • mechanism of action

Published Papers (1 paper)

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Research

15 pages, 1290 KiB  
Article
Brilacidin as a Broad-Spectrum Inhibitor of Enveloped, Acutely Infectious Viruses
by Carol A. Anderson, Michael D. Barrera, Niloufar A. Boghdeh, Miata Smith, Farhang Alem and Aarthi Narayanan
Microorganisms 2024, 12(1), 54; https://doi.org/10.3390/microorganisms12010054 - 28 Dec 2023
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Abstract
Alphaviruses, belonging to the Togaviridae family, and bunyaviruses, belonging to the Paramyxoviridae family, are globally distributed and lack FDA-approved vaccines and therapeutics. The alphaviruses Venezuelan equine encephalitis virus (VEEV) and eastern equine encephalitis virus (EEEV) are known to cause severe encephalitis, whereas Sindbis [...] Read more.
Alphaviruses, belonging to the Togaviridae family, and bunyaviruses, belonging to the Paramyxoviridae family, are globally distributed and lack FDA-approved vaccines and therapeutics. The alphaviruses Venezuelan equine encephalitis virus (VEEV) and eastern equine encephalitis virus (EEEV) are known to cause severe encephalitis, whereas Sindbis virus (SINV) causes arthralgia potentially persisting for years after initial infection. The bunyavirus Rift Valley Fever virus (RVFV) can lead to blindness, liver failure, and hemorrhagic fever. Brilacidin, a small molecule that was designed de novo based on naturally occurring host defensins, was investigated for its antiviral activity against these viruses in human small airway epithelial cells (HSAECs) and African green monkey kidney cells (Veros). This testing was further expanded into a non-enveloped Echovirus, a Picornavirus, to further demonstrate brilacidin’s effect on early steps of the viral infectious cycle that leads to inhibition of viral load. Brilacidin demonstrated antiviral activity against alphaviruses VEEV TC-83, VEEV TrD, SINV, EEEV, and bunyavirus RVFV. The inhibitory potential of brilacidin against the viruses tested in this study was dependent on the dosing strategy which necessitated compound addition pre- and post-infection, with addition only at the post-infection stage not eliciting a robust inhibitory response. The inhibitory activity of brilacidin was only modest in the context of the non-enveloped Picornavirus Echovirus, suggesting brilacidin may be less potent against non-enveloped viruses. Full article
(This article belongs to the Special Issue Emerging Viruses and Antiviral Drugs 2.0)
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