Dinh Hieu, Zhang Xiaohu, Sweeney Joyce, Yang Yang, He Yun, Dhawane Abasaheb, Iyer Suri S
788 Petit Science Center, Department of Chemistry, Center for Diagnostics and Therapeutics, Georgia State University , Atlanta, Georgia 30302, United States.
Anal Chem. 2014 Aug 19;86(16):8238-44. doi: 10.1021/ac501624v. Epub 2014 Aug 1.
We have developed a panel of synthetic glycans as receptor mimics for the specific capture of influenza viruses. The glycans were printed onto commercial glass slides using a free amine at the end of a spacer to generate a small focused microarray. The microarray was evaluated for its ability to capture three different strains of influenza A virus, two H1N1, A/Brisbane/59/2007 and A/Solomon Islands/3/2006 and one H3N2, A/Aichi/2/1968. We observed an excellent detection ability with some compounds exhibiting clinically relevant (10(1) plaque forming units) limit of detection. We also tested the drug susceptibility of current antivirals, Zanamivir and Ostelamivir using this microarray and could determine antiviral resistance for these strains.
我们开发了一组合成聚糖作为受体模拟物,用于特异性捕获流感病毒。使用间隔物末端的游离胺将聚糖打印在商用载玻片上,以生成小型聚焦微阵列。对该微阵列捕获三种不同甲型流感病毒株的能力进行了评估,其中两种H1N1病毒株,分别为A/布里斯班/59/2007和A/所罗门群岛/3/2006,以及一种H3N2病毒株,A/爱知/2/1968。我们观察到一些化合物具有出色的检测能力,其检测限达到临床相关水平(10¹ 噬斑形成单位)。我们还使用该微阵列测试了当前抗病毒药物扎那米韦和奥司他韦的药敏性,并能够确定这些病毒株的抗病毒耐药性。