4.6 Article

Antiviral Screen against Canine Distemper Virus-Induced Membrane Fusion Activity

期刊

VIRUSES-BASEL
卷 13, 期 1, 页码 -

出版社

MDPI
DOI: 10.3390/v13010128

关键词

CDV; cell-based fusion assay; envelope glycoproteins; host cell receptor; inhibitor discovery

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资金

  1. University of Bern
  2. Swiss National Science Foundation [SNSF CRSII5_183481]
  3. Gottfried and Julia Bangerter-Rhyner Foundation
  4. SNSF/NCCR Chemical Biology

向作者/读者索取更多资源

Canine distemper virus (CDV) is a close relative of the human pathogen measles virus (MeV) and causes severe diseases in dogs and other carnivores. Vaccinations are available to prevent the disease, but the importance of antivirals against CDV is highlighted by occasional vaccination failures. A cell-based fusion assay identified two membrane fusion inhibitors, showing potential for new therapeutic alternatives against CDV.
Canine distemper virus (CDV), a close relative of the human pathogen measles virus (MeV), is an enveloped, negative sense RNA virus that belongs to the genus Morbillivirus and causes severe diseases in dogs and other carnivores. Although the vaccination is available as a preventive measure against the disease, the occasional vaccination failure highlights the importance of therapeutic alternatives such as antivirals against CDV. The morbilliviral cell entry system relies on two interacting envelope glycoproteins: the attachment (H) and fusion (F) proteins. Here, to potentially discover novel entry inhibitors targeting CDV H, F and/or the cognate receptor: signaling lymphocyte activation molecule (SLAM) proteins, we designed a quantitative cell-based fusion assay that matched high-throughput screening (HTS) settings. By screening two libraries of small molecule compounds, we successfully identified two membrane fusion inhibitors (F2736-3056 and F2261-0043). Although both inhibitors exhibited similarities in structure and potency with the small molecule compound 3G (an AS-48 class morbilliviral F-protein inhibitor), F2736-3056 displayed improved efficacy in blocking fusion activity when a 3G-escape variant was employed. Altogether, we present a cell-based fusion assay that can be utilized not only to discover antiviral agents against CDV but also to dissect the mechanism of morbilliviral-mediated cell-binding and cell-to-cell fusion activity.

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