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与抗 SARS-CoV-2 药物奈玛特韦相关的耐药突变:选择而非诱导。

Resistance-associated mutations to the anti-SARS-CoV-2 agent nirmatrelvir: Selection not induction.

机构信息

IHU Méditerranée Infection, 19-21 boulevard Jean Moulin, Marseille, France.

Aix-Marseille Univ., Institut de Recherche pour le Développement (IRD), Microbes Evolution Phylogeny and Infections (MEPHI), 27 boulevard Jean Moulin, Marseille, France.

出版信息

J Med Virol. 2024 Feb;96(2):e29462. doi: 10.1002/jmv.29462.

Abstract

Mutations associated with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) resistance to antiprotease nirmatrelvir were reported. We aimed to detect them in SARS-CoV-2 genomes and quasispecies retrieved in our institute before drug availability in January 2022 and to analyze the impact of mutations on protease (3CLpro) structure. We sought for 38 3CLpro nirmatrelvir resistance mutations in a set of 62 673 SARS-CoV-2 genomes obtained in our institute from respiratory samples collected between 2020 and 2023 and for these mutations in SARS-CoV-2 quasispecies for 90 samples collected in 2020, using Python. SARS-CoV-2 protease with major mutation E166V was generated with Swiss Pdb Viewer and Molegro Molecular Viewer. We detected 22 (58%) of the resistance-associated mutations in 417 (0.67%) of the genomes analyzed; 325 (78%) of these genomes had been obtained from samples collected in 2020-2021. APOBEC signatures were found for 12/22 mutations. We also detected among viral quasispecies from 90 samples some minority reads harboring any of 15 nirmatrelvir resistance mutations, including E166V. Also, we predicted that E166V has a very limited effect on 3CLpro structure but may prevent drug attachment. Thus, we evidenced that mutations associated with nirmatrelvir resistance pre-existed in SARS-CoV-2 before drug availability. These findings further warrant SARS-CoV-2 genomic surveillance and SARS-CoV-2 quasispecies characterization.

摘要

与严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)对蛋白酶抑制剂奈玛特韦耐药相关的突变已被报道。我们旨在检测在我们研究所获得的 SARS-CoV-2 基因组和准种中是否存在这些突变,这些基因组和准种是在 2022 年 1 月药物可用之前收集的,并分析突变对蛋白酶(3CLpro)结构的影响。我们使用 Python 在我们研究所收集的 62673 份 SARS-CoV-2 基因组中寻找了 38 种 3CLpro 奈玛特韦耐药突变,并在 2020 年收集的 90 份样本的 SARS-CoV-2 准种中寻找了这些突变。使用 Swiss Pdb Viewer 和 Molegro Molecular Viewer 生成了带有主要突变 E166V 的 SARS-CoV-2 蛋白酶。我们在分析的 417 个基因组中检测到了 22 个(58%)与耐药相关的突变;其中 325 个(78%)基因组是在 2020-2021 年期间收集的。在 12/22 个突变中发现了 APOBEC 签名。我们还在 90 个样本的病毒准种中检测到了少数含有 15 种奈玛特韦耐药突变之一的读段,包括 E166V。此外,我们预测 E166V 对 3CLpro 结构的影响非常有限,但可能会阻止药物附着。因此,我们证明了在药物可用之前,与奈玛特韦耐药相关的突变已经存在于 SARS-CoV-2 中。这些发现进一步证明了需要对 SARS-CoV-2 基因组进行监测,并对 SARS-CoV-2 准种进行特征描述。

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