Laboratory of Virology, National Institute for Infectious Diseases Lazzaro Spallanzani IRCCS, Rome, Italy.
Department of Biology, University of Rome Tor Vergata, Rome, Italy.
J Med Virol. 2024 May;96(5):e29642. doi: 10.1002/jmv.29642.
Molnupiravir, an oral direct-acting antiviral effective in vitro against SARS-CoV-2, has been largely employed during the COVID-19 pandemic, since December 2021. After marketing and widespread usage, a progressive increase in SARS-CoV-2 lineages characterized by a higher transition/transversion ratio, a characteristic signature of molnupiravir action, appeared in the Global Initiative on Sharing All Influenza Data (GISAID) and International Nucleotide Sequence Database Collaboration (INSDC) databases. Here, we assessed the drug effects by SARS-CoV-2 whole-genome sequencing on 38 molnupiravir-treated persistently positive COVID-19 outpatients tested before and after treatment. Seventeen tixagevimab/cilgavimab-treated outpatients served as controls. Mutational analyses confirmed that SARS-CoV-2 exhibits an increased transition/transversion ratio seven days after initiation of molnupiravir. Moreover we observed an increased G->A ratio compared to controls, which was not related to apolipoprotein B mRNAediting enzyme, catalytic polypeptide-like (APOBEC) activity. In addition, we demonstrated for the first time an increased diversity and complexity of the viral quasispecies.
莫努匹韦是一种在体外对 SARS-CoV-2 有效的口服直接作用抗病毒药物,自 2021 年 12 月以来,在 COVID-19 大流行期间得到了广泛应用。在上市和广泛使用后,在全球流感数据共享倡议 (GISAID) 和国际核苷酸序列数据库合作组织 (INSDC) 数据库中,出现了具有更高转换/颠换比的 SARS-CoV-2 谱系的逐渐增加,这是莫努匹韦作用的特征标志。在这里,我们通过对 38 名接受莫努匹韦治疗的持续检测呈阳性的 COVID-19 门诊患者在治疗前后进行的 SARS-CoV-2 全基因组测序来评估药物效果。17 名接受替沙格韦单抗/西加韦单抗治疗的门诊患者作为对照。突变分析证实,在开始使用莫努匹韦七天后,SARS-CoV-2 的转换/颠换比增加。此外,与对照组相比,我们观察到 G->A 比值增加,这与载脂蛋白 B mRNA 编辑酶,催化多肽样 (APOBEC) 活性无关。此外,我们首次证明了病毒准种的多样性和复杂性增加。