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H274Y 取代对反向遗传流感 A 病毒中 N1、N4、N5 和 N8 神经氨酸酶酶学特性和表达的影响。

Impact of the H274Y Substitution on N1, N4, N5, and N8 Neuraminidase Enzymatic Properties and Expression in Reverse Genetic Influenza A Viruses.

机构信息

Virpath Unit, CIRI, Inserm U1111, CNRS, UMR5308, ENS Lyon, Université Claude Bernard Lyon 1, F-69372 Lyon, France.

Centre National de Référence des Virus des Infections Respiratoires, Groupement Hospitalier Nord, Hospices Civils de Lyon, F-69317 Lyon CEDEX 04, France.

出版信息

Viruses. 2024 Mar 1;16(3):388. doi: 10.3390/v16030388.

Abstract

The H274Y substitution (N2 numbering) in neuraminidase (NA) N1 confers oseltamivir resistance to A(H1N1) influenza viruses. This resistance has been associated with reduced N1 expression using transfected cells, but the effect of this substitution on the enzymatic properties and on the expression of other group-1-NA subtypes is unknown. The aim of the present study was to evaluate the antiviral resistance, enzymatic properties, and expression of wild-type (WT) and H274Y-substituted NA for each group-1-NA. To this end, viruses with WT or H274Y-substituted NA (N1pdm09 or avian N4, N5 or N8) were generated by reverse genetics, and for each reverse-genetic virus, antiviral susceptibility, NA affinity (Km), and maximum velocity (Vm) were measured. The enzymatic properties were coupled with NA quantification on concentrated reverse genetic viruses using mass spectrometry. The H274Y-NA substitution resulted in highly reduced inhibition by oseltamivir and normal inhibition by zanamivir and laninamivir. This resistance was associated with a reduced affinity for MUNANA substrate and a conserved Vm in all viruses. NA quantification was not significantly different between viruses carrying WT or H274Y-N1, N4 or N8, but was lower for viruses carrying H274Y-N5 compared to those carrying a WT-N5. In conclusion, the H274Y-NA substitution of different group-1-NAs systematically reduced their affinity for MUNANA substrate without a significant impact on NA Vm. The impact of the H274Y-NA substitution on viral NA expression was different according to the studied NA.

摘要

神经氨酸酶(NA)N1 中的 H274Y 取代(N2 编号)赋予 A(H1N1)流感病毒对奥司他韦的耐药性。这种耐药性与转染细胞中 N1 表达减少有关,但该取代对其他 1 型 NA 亚型的酶学特性和表达的影响尚不清楚。本研究旨在评估野生型(WT)和 H274Y 取代 NA 的抗病毒耐药性、酶学特性和表达,用于每组 1 型 NA。为此,通过反向遗传学生成了具有 WT 或 H274Y 取代 NA(N1pdm09 或禽 N4、N5 或 N8)的病毒,对于每种反向遗传病毒,测量了抗病毒敏感性、NA 亲和力(Km)和最大速度(Vm)。将酶学特性与使用质谱法浓缩的反向遗传病毒上的 NA 定量相结合。H274Y-NA 取代导致奥司他韦高度抑制和扎那米韦和拉尼米韦正常抑制。这种耐药性与对 MUNANA 底物的亲和力降低以及所有病毒中保守的 Vm 相关。携带 WT 或 H274Y-N1、N4 或 N8 的病毒之间的 NA 定量没有显着差异,但与携带 WT-N5 的病毒相比,携带 H274Y-N5 的病毒的 NA 定量较低。总之,不同 1 型 NA 的 H274Y-NA 取代系统地降低了它们对 MUNANA 底物的亲和力,而对 NA Vm 没有显着影响。H274Y-NA 取代对病毒 NA 表达的影响因研究的 NA 而异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/894b/10975200/aafa11ab94d2/viruses-16-00388-g001.jpg

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