tetano
Editor, Senior Moderator
Npj Viruses
. 2024 Jun 24;2(1):23.
doi: 10.1038/s44298-024-00028-2.
Study of key residues in MERS-CoV and SARS-CoV-2 main proteases for resistance against clinically applied inhibitors nirmatrelvir and ensitrelvir
Laura Krismer[SUP] 1 [/SUP], Helge Schöppe[SUP] #[/SUP][SUP] 2 [/SUP], Stefanie Rauch[SUP] #[/SUP][SUP] 1 [/SUP], David Bante[SUP] 1 [/SUP], Bernhard Sprenger[SUP] 3 [/SUP], Andreas Naschberger[SUP] 4 [/SUP], Francesco Costacurta[SUP] 1 [/SUP], Anna Fürst[SUP] 5 [/SUP], Anna Sauerwein[SUP] 1 [/SUP], Bernhard Rupp[SUP] 6 [/SUP], Teresa Kaserer[SUP] 2 [/SUP], Dorothee von Laer[SUP] 1 [/SUP], Emmanuel Heilmann[SUP] 7 [/SUP]
Affiliations
The Middle East Respiratory Syndrome Coronavirus (MERS-CoV) is an epidemic, zoonotically emerging pathogen initially reported in Saudi Arabia in 2012. MERS-CoV has the potential to mutate or recombine with other coronaviruses, thus acquiring the ability to efficiently spread among humans and become pandemic. Its high mortality rate of up to 35% and the absence of effective targeted therapies call for the development of antiviral drugs for this pathogen. Since the beginning of the SARS-CoV-2 pandemic, extensive research has focused on identifying protease inhibitors for the treatment of SARS-CoV-2. Our intention was therefore to assess whether these protease inhibitors are viable options for combating MERS-CoV. To that end, we used previously established protease assays to quantify inhibition of SARS-CoV-2, MERS-CoV and other main proteases. Nirmatrelvir inhibited several of these proteases, whereas ensitrelvir was less broadly active. To simulate nirmatrelvir's clinical use against MERS-CoV and subsequent resistance development, we applied a safe, surrogate virus-based system. Using the surrogate virus, we previously selected hallmark mutations of SARS-CoV-2-M[SUP]pro[/SUP], such as T21I, M49L, S144A, E166A/K/V and L167F. In the current study, we selected a pool of MERS-CoV-M[SUP]pro[/SUP] mutants, characterized the resistance and modelled the steric effect of catalytic site mutants S142G, S142R, S147Y and A171S.
. 2024 Jun 24;2(1):23.
doi: 10.1038/s44298-024-00028-2.
Study of key residues in MERS-CoV and SARS-CoV-2 main proteases for resistance against clinically applied inhibitors nirmatrelvir and ensitrelvir
Laura Krismer[SUP] 1 [/SUP], Helge Schöppe[SUP] #[/SUP][SUP] 2 [/SUP], Stefanie Rauch[SUP] #[/SUP][SUP] 1 [/SUP], David Bante[SUP] 1 [/SUP], Bernhard Sprenger[SUP] 3 [/SUP], Andreas Naschberger[SUP] 4 [/SUP], Francesco Costacurta[SUP] 1 [/SUP], Anna Fürst[SUP] 5 [/SUP], Anna Sauerwein[SUP] 1 [/SUP], Bernhard Rupp[SUP] 6 [/SUP], Teresa Kaserer[SUP] 2 [/SUP], Dorothee von Laer[SUP] 1 [/SUP], Emmanuel Heilmann[SUP] 7 [/SUP]
Affiliations
- PMID: 41731094
- DOI: 10.1038/s44298-024-00028-2
The Middle East Respiratory Syndrome Coronavirus (MERS-CoV) is an epidemic, zoonotically emerging pathogen initially reported in Saudi Arabia in 2012. MERS-CoV has the potential to mutate or recombine with other coronaviruses, thus acquiring the ability to efficiently spread among humans and become pandemic. Its high mortality rate of up to 35% and the absence of effective targeted therapies call for the development of antiviral drugs for this pathogen. Since the beginning of the SARS-CoV-2 pandemic, extensive research has focused on identifying protease inhibitors for the treatment of SARS-CoV-2. Our intention was therefore to assess whether these protease inhibitors are viable options for combating MERS-CoV. To that end, we used previously established protease assays to quantify inhibition of SARS-CoV-2, MERS-CoV and other main proteases. Nirmatrelvir inhibited several of these proteases, whereas ensitrelvir was less broadly active. To simulate nirmatrelvir's clinical use against MERS-CoV and subsequent resistance development, we applied a safe, surrogate virus-based system. Using the surrogate virus, we previously selected hallmark mutations of SARS-CoV-2-M[SUP]pro[/SUP], such as T21I, M49L, S144A, E166A/K/V and L167F. In the current study, we selected a pool of MERS-CoV-M[SUP]pro[/SUP] mutants, characterized the resistance and modelled the steric effect of catalytic site mutants S142G, S142R, S147Y and A171S.