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2009 年至 2014 年期间中国广东地区甲型 H1N1/季节性 H3N2 及乙型流感病毒对奥司他韦的敏感性。

Susceptibility of influenza A(H1N1)/pdm2009, seasonal A(H3N2) and B viruses to Oseltamivir in Guangdong, China between 2009 and 2014.

机构信息

Department of Pharmaceutical Engineering, South China Agricultural University, Guangzhou, 510640, China.

Shantou University Medical College, Shantou, 515041, Guangdong, China.

出版信息

Sci Rep. 2017 Aug 16;7(1):8488. doi: 10.1038/s41598-017-08282-6.

Abstract

Nasopharyngeal swabs were collected from patients through the influenza surveillance network of the CDC of Guangdong. All specimens between 2009 and 2014 were checked for influenza virus using MDCK cells and further subtyped. Of those collected, 542 H1N1pdm09, 230 A(H3N2)and 448 B viruses selected at random were subjected to fluorescence-based NAI assays. Viral RNA was extracted from resistant isolates, and their NA genes were amplified by RT-PCR. Alignment of nucleotides and amino acids was performed. We performed structural modelling and simulations of mutants using Modeller 9.x and AutoDock and analyzed conformations and binding affinities. All tested seasonal type B and H3N2 viruses from 2009 to 2014 remained sensitive to oseltamivir. However, there were five strains (out of 198 tested isolates acquired between June and September 2013) that were resistant to oseltamivir. Another three resistant strains were identified among isolates from March to April 2014. We found that 2013/2014 oseltamivir-resistant strains and 2012/2013/2014 oseltamivir-sensitive strains had all or some of the following mutations: N44S, N200S,V241I, I321V,N369K, N386 K and K432E. MutationsV241I, N369K, N386K and K432E, alone or in conjunction with H275Y, had a significant impact on the binding pattern and affinity of oseltamivir for neuraminidase, rendering neuraminidase less susceptible.

摘要

从广东省疾病预防控制中心的流感监测网络中收集了患者的鼻咽拭子。使用 MDCK 细胞对所有在 2009 年至 2014 年间采集的标本进行流感病毒检测,并进一步进行亚型检测。随机选择了 542 株 H1N1pdm09、230 株 A(H3N2)和 448 株 B 病毒进行基于荧光的 NAI 检测。从耐药分离株中提取病毒 RNA,并通过 RT-PCR 扩增其 NA 基因。对核苷酸和氨基酸进行了比对。我们使用 Modeller 9.x 和 AutoDock 对突变体进行了结构建模和模拟,并分析了构象和结合亲和力。所有测试的 2009 年至 2014 年季节性 B 型和 H3N2 病毒对奥司他韦仍然敏感。然而,在 2013 年 6 月至 9 月期间获得的 198 株分离株中有 5 株对奥司他韦耐药。在 2014 年 3 月至 4 月期间获得的分离株中还发现了另外 3 株耐药株。我们发现,2013/2014 年奥司他韦耐药株和 2012/2013/2014 年奥司他韦敏感株都具有或具有以下某些突变:N44S、N200S、V241I、I321V、N369K、N386 K 和 K432E。突变 V241I、N369K、N386K 和 K432E 单独或与 H275Y 一起,对奥司他韦与神经氨酸酶的结合模式和亲和力有显著影响,使神经氨酸酶的敏感性降低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8672/5559489/bbd18890cf88/41598_2017_8282_Fig1_HTML.jpg

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