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一种新型轮状病毒反向遗传学平台支持外源基因的灵活插入,并能快速开发高通量中和测定法。

A Novel Rotavirus Reverse Genetics Platform Supports Flexible Insertion of Exogenous Genes and Enables Rapid Development of a High-Throughput Neutralization Assay.

机构信息

Department of Infectious Diseases and Vaccines, Merck & Co., Inc., West Point, PA 19486, USA.

Department of Quantitative Biosciences, Merck & Co., Inc., West Point, PA 19486, USA.

出版信息

Viruses. 2023 Sep 30;15(10):2034. doi: 10.3390/v15102034.

Abstract

Despite the success of rotavirus vaccines, rotaviruses remain one of the leading causes of diarrheal diseases, resulting in significant childhood morbidity and mortality, especially in low- and middle-income countries. The reverse genetics system enables the manipulation of the rotavirus genome and opens the possibility of using rotavirus as an expression vector for heterologous proteins, such as vaccine antigens and therapeutic payloads. Here, we demonstrate that three positions in rotavirus genome-the C terminus of NSP1, NSP3 and NSP5-can tolerate the insertion of reporter genes. By using rotavirus expressing GFP, we develop a high-throughput neutralization assay and reveal the pre-existing immunity against rotavirus in humans and other animal species. Our work shows the plasticity of the rotavirus genome and establishes a high-throughput assay for interrogating humoral immune responses, benefiting the design of next-generation rotavirus vaccines and the development of rotavirus-based expression platforms.

摘要

尽管轮状病毒疫苗取得了成功,但轮状病毒仍然是导致腹泻病的主要原因之一,尤其是在低收入和中等收入国家,导致儿童发病率和死亡率显著上升。反向遗传学系统使轮状病毒基因组的操作成为可能,并为使用轮状病毒作为异源蛋白(如疫苗抗原和治疗有效载荷)的表达载体开辟了可能性。在这里,我们证明轮状病毒基因组的三个位置 - NSP1、NSP3 和 NSP5 的 C 末端 - 可以耐受报告基因的插入。通过使用表达 GFP 的轮状病毒,我们开发了一种高通量中和测定法,并揭示了人类和其他动物物种中针对轮状病毒的预先存在的免疫。我们的工作表明了轮状病毒基因组的可塑性,并建立了一种高通量测定法来研究体液免疫反应,这有利于下一代轮状病毒疫苗的设计和基于轮状病毒的表达平台的开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbde/10611407/4adfa00620ee/viruses-15-02034-g001.jpg

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