荧光唾液酸酶显像法高效检测和分离神经氨酸酶抑制剂耐药流感病毒。

The Japanese journal of antibiotics Pub Date : 2016-12-01
Yuuki Kurebayashi
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引用次数: 0

摘要

甲型流感和乙型流感病毒具有一种酶“唾液酸酶”,可以从糖链上切割末端唾液酸。这些病毒唾液酸酶蛋白在病毒感染的细胞上高度表达。我们开发了唾液酸酶成像探针“BTP3-Neu5Ac”,可以进行唾液酸酶活性的组织化学荧光染色。BTP3-Neu5Ac能够对这些病毒感染的细胞进行快速、简便的荧光成像,不需要特异性抗体和细胞固定。此外,抗流感药物(唾液酸酶抑制剂)与BTP3-Neu5Ac联合使用可实现选择性荧光成像检测和高效分离耐药病毒。耐药病毒荧光成像将成为研究耐药机制、监测耐药病毒的有力手段。本文介绍了一种新型的病毒唾液酸酶活性荧光成像工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High efficiency method of detection and isolation of neuraminidase inhibitor resistant influenza viruses by fluorescence sialidase imaging.

Influenza A and B viruses possess an enzyme "sialidase" that cleavages terminal sialic acid from glycochains. These viral sialidase proteins are highly expressed on the virus infected cells. We developed sialidase imaging probe "BTP3-Neu5Ac" that enables histochemical fluorescence staining of sialidase activity. BTP3-Neu5Ac was able to perform speedy and easy fluorescence imaging of these virus infected cells, with no needs of specific antibody and cell fixation. In addition, combination use of anti-influenza drugs (sialidase inhibitors) and BTP3-Neu5Ac resulted in selective fluorescence imaging for detection and high-efficiency isolation of drug-resistant virus. Fluorescence imaging of drug-resistant virus will be a powerful method for study of the drug-resistance mechanism, for monitoring of drug-resistant viruses. A novel tool for fluorescence imaging of viral sialidase activity is described in this review.

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