AI Article Synopsis

  • Canine distemper virus (CDV) is an enveloped RNA virus that affects dogs and other carnivores, and while vaccines exist, they sometimes fail, making antiviral treatments necessary.
  • Researchers developed a quantitative cell-based fusion assay to discover inhibitors targeting the virus's entry proteins (H and F) and its receptor, SLAM.
  • Two effective membrane fusion inhibitors were identified from small molecule libraries, particularly F2736-3056, which outperformed a known compound in blocking fusion activity, providing tools for further research on CDV's mechanisms and new treatments.

Article Abstract

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 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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7831055PMC
http://dx.doi.org/10.3390/v13010128DOI Listing

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