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Details

Autor(en) / Beteiligte
Titel
Inhibitors of dihydroorotate dehydrogenase cooperate with molnupiravir and N4-hydroxycytidine to suppress SARS-CoV-2 replication
Ist Teil von
  • iScience, 2022-05, Vol.25 (5), p.104293-104293, Article 104293
Ort / Verlag
United States: Elsevier Inc
Erscheinungsjahr
2022
Quelle
Free E-Journal (出版社公開部分のみ)
Beschreibungen/Notizen
  • The nucleoside analog N4-hydroxycytidine (NHC) is the active metabolite of the prodrug molnupiravir, which has been approved for the treatment of COVID-19. SARS-CoV-2 incorporates NHC into its RNA, resulting in defective virus genomes. Likewise, inhibitors of dihydroorotate dehydrogenase (DHODH) reduce virus yield upon infection, by suppressing the cellular synthesis of pyrimidines. Here, we show that NHC and DHODH inhibitors strongly synergize in the inhibition of SARS-CoV-2 replication in vitro. We propose that the lack of available pyrimidine nucleotides upon DHODH inhibition increases the incorporation of NHC into nascent viral RNA. This concept is supported by the rescue of virus replication upon addition of pyrimidine nucleosides to the media. DHODH inhibitors increased the antiviral efficiency of molnupiravir not only in organoids of human lung, but also in Syrian Gold hamsters and in K18-hACE2 mice. Combining molnupiravir with DHODH inhibitors may thus improve available therapy options for COVID-19. [Display omitted] •Molnupiravir and DHODH inhibitors are approved drugs, facilitating clinical testing•The combination may allow lower drug doses to decrease possible toxic effects•Inhibitors of nucleotide biosynthesis may boost antiviral nucleoside analogs Virology; Drugs
Sprache
Englisch
Identifikatoren
ISSN: 2589-0042
eISSN: 2589-0042
DOI: 10.1016/j.isci.2022.104293
Titel-ID: cdi_doaj_primary_oai_doaj_org_article_3893fdc86a5b4569a07925c5deb2bfb2
Format
Schlagworte
Drugs, Virology

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