Published in Microorganisms: Z-Tyr-Ala-CHN2, a Cathepsin L Inhibitor with Broad-Spectrum Cell-Specific Activity against Coronaviruses

The CARE partner Janssen Pharmaceutica in collaboration with University Utrecht, KU Leuven and Goethe University Frankfurt has published a paper about the discovery of a small molecule, Z-Tyr-Ala-CHN2, which was identified in a cell-based antiviral screen. The molecule exerts sub-micromolar antiviral activity against SARS-CoV-2, SARS-CoV-1, and human coronavirus 229E at the early phase of the infection cycle, which is in line with the observation that the molecule inhibits cathepsin L. The activity profile of Z-Tyr-Ala-CHN2 makes it an interesting tool compound for studying the biology of coronavirus entry and replication.

To learn more, click here: Identification of Z-Tyr-Ala-CHN2, a Cathepsin L Inhibitor with Broad-Spectrum Cell-Specific Activity against Coronaviruses, including SARS-CoV-2

CARE presentation at 19th Annual PEGS Boston conference and expo

Are you going to the 19th Annual PEGS Boston conference & Expo: The Essential Protein Engineering and Cell Therapy Summit next week? If so, you will have the opportunity to discover how to identify pre-lead antibodies that have multiple epitopes on the SARS-CoV-2 spike protein using Carterra’s high-throughput epitope binning. Do not hesitate to visit the poster by CARE partner Takeda during one of the Poster Viewing session.

Title of the presentation: Identification of Binning Diversity and Binding Properties of SARS-CoV-2 Antibodies Using Carterra

Presenter: Hazal B. Kose, Ruiyang Xuee

Published in Antiviral Res: A VeroE6 cell line not requiring Pgp inhibitors to evaluate SARS-CoV-2 antivirals

Cell culture virus replication systems are essential for the study of virus replication and pathogenesis, antiviral drug testing, and virus research. Vero cells are one of the cell lines used for drug discovery as they are susceptible to SARS-CoV-2 infection – as well as to SARS-CoV-1 and MERS viruses -, easy to maintain, offer high levels of infectivity, and support efficient SARS-CoV-2 replication and virus production.

However, Vero cells express high levels of multidrug resistance protein 1 (MDR1), also named Pgp (P-glycoprotein), an ATP-dependent efflux pump, which necessitates the inclusion of a Pgp inhibitor in the cell culture to prevent tested compounds from being exported out of cells, affecting the antiviral activity as well as interpretation of data. To address this, CARE partner Pfizer used gene editing technology to generate a Pgp gene knockout VeroE6 cell line.

The VeroE6-Pgp-KO cells no longer expressed the Pgp protein and show significantly reduced efflux transporter activity. When remdesivir and nirmatrevil, two known Pgp substrates, were tested in this cell line, both drugs showed antiviral activities similar to that observed in the presence of the Pgp inhibitor.

This newly established VeroE6-Pgp-KO cell line adds a new in vitro virus infection system for SARS-CoV-2 – and possibly other viruses – to test antiviral therapies without a need to control the Pgp activity, and thus with less data variation and failed assays.

To learn more, click here: Generation of a VeroE6 Pgp gene knock out cell line and its use in SARS-CoV-2 antiviral study

Published in iScience: A new  optimized SARS-CoV-2 phenotypic screening platform

The CARE partner Goethe University Frankfurt Institute of Medical Virology, published a paper reporting on a novel phenotypic screening platform for the identification of drug candidates with activity against SARS-CoV-2 and other coronaviruses. This successful proof of concept was based on the determination of caspase 3/7 activity using the one-step Caspase-Glo 3/7 Assay System as readout. This platform uses the Caco-2-F03 cell line which demonstrated susceptibility to a broad range of SARS-CoV-2 without being affected by phospholipidosis, a known cause of false-positive hits, and is also considered suitable for neutralisation assays and phenotypic resistance testing.

To learn more, click here: Identification of novel antiviral drug candidates using an optimized SARS-CoV-2 phenotypic screening platform

Published in in Journal of Virology: A new mouse model for preclinical evaluation of potential antivirals

As ancestral SARS-CoV-2 viruses are not able to bind to the mouse ACE2 receptor, establishment of SARS-CoV-2 mouse models has been limited to the use of mouse-adapted viruses or genetically modified mice. In parallel, Syrian hamsters are considered one of the best small animal models available for SARS-CoV-2 since SARS-CoV-2 binds efficiently to the hamster ACE2.

Interestingly, some of the variants of concern, such as the Beta B.1.351 variant, show an improved binding to the mouse receptor. The CARE partner KU Leuven (KUL, Belgium) exploited this difference to establish a SARS-CoV-2 Beta B.1.351 variant infection model in an immunodeficient mouse model, i.e., SCID mice, with the aim to develop a robust SARS-CoV-2 mouse infection model for preclinical evaluation of potential antivirals.

The model’s robustness to study the efficacy of small-molecule inhibitors of SARS-CoV-2 infection was confirmed by its sensitivity to molnupiravir or nirmatrelvir and by more efficient replication of the Beta SARS-CoV-2 variant in SCID mice than in wild-type mice.

This SARS-CoV-2 SCID mouse infection model offers an advantage in comparison to other SARS-CoV-2 mouse models – no need to use mouse-adapted virus strains or genetically modified mice – and to the hamster models as it requires lower amounts of drugs, less space, etc..  On the other hand, a limitation is that mice are only susceptible to the Beta variant and that since small-molecule inhibitors should have equipotent activity against all variants, this will be of limited concern for studies with such drugs.

To learn more, click here: A SCID mouse model to evaluate the efficacy of antivirals against SARS-CoV-2 infection

Published in Nature: First insights into the Porcine Deltacoronavirus spike
19 September 2024
Published in Nature: First insights into the Porcine Deltacoronavirus spike Further to CARE’s SARS-CoV-2 research, CARE partner Utrecht University (UU) has studied the Porcine Deltacoronavirus (PDCoV) spike, providing crucial insights for developing antiviral strategies. PDCoV, an emerging enteric pathogen in pigs, has recently been detected in children with acute febrile illness. PDCoV enters cells by [...]