Single cell heterogeneity of influenza A virus genetic diversity and host adaptation using drop-based microfluidics

项目摘要 当突变使宿主适应时，可能会出现新的甲型大流行性流感病毒(IAV)株。突变 在病毒涌现和人畜共患感染中，克服宿主范围限制很重要。人畜共患病溢出效应 感染禽流感病毒亚型的人，如H5N1和H7N9，死亡率高达60%。而当 重大进展已经确定了许多突变，使IAV能够适应新的宿主物种，我们有一个 对病毒复制过程中产生的病毒突变的深度了解不足。定义 病毒突变的异质性将揭示使人畜共患病溢出的病毒基因多样性。 至关重要的是，人类的IAV感染发生在呼吸道的异源细胞群中，这些细胞群与 与病毒传播的可能性不同。对这两种不同细胞类型的单细胞分析 人类和禽类IAV株将使我们能够探索病毒株和细胞类型如何影响病毒多样性。 基于液滴的微流体是一种将宿主细胞和病毒在皮升内分开的方法。 确定液滴大小，创建数百万个微环境，从而实现高通量分析。基于Drop的 因此，微流控技术为从快速进化的RNA中研究病毒遗传多样性提供了一个理想的平台 实验室里的病毒。我们的长期目标是了解IAV的演变导致宿主 适应、毒力、传播，最终是人畜共患病的传播。开始解决这一长期问题 目的用1评价单细胞IAV基因组的异质性。量化产生的遗传多样性 来自禽类和季节性人类IAV对单个人类原代细胞的感染和2。)表演 在单细胞水平上连续传代IAV病毒的进化研究。这两个是独立的，但是 互补的目标旨在了解：(目标1)特定细胞类型如何影响病毒遗传 多样性和人畜共患病风险，以及(目标2)病毒多样性在系统和种群水平上如何演变 瓶颈被改变了。拟议的研究将通过以下方式广泛影响单细胞病毒学领域 描述病毒多样性在病毒传播、传播和进化中扮演的角色。这些研究 将产生对病毒宿主细胞动力学的基本机械见解，这可能有助于开发 可以针对快速进化的IAV和其他RNA病毒的有效疫苗和治疗方法。

Project Summary New pandemic influenza A virus (IAV) strains can arise when mutations enable host adaptation. Mutations that overcome host range restrictions are important in viral emergence and zoonotic infections. Zoonotic spillover into humans with avian IAV subtypes, such as H5N1 and H7N9, have mortality rates as high as 60%. While significant progress has identified many mutations that allow IAV to adapt to new host species, we have an incomplete understanding of the depth of viral mutations generated during viral replication. Defining the heterogeneity of viral mutations will shed light on the viral genetic diversity that enables zoonotic spillover. Critically, IAV infection in humans occurs in heterologous cell populations in the respiratory tract that correlate differently with the likelihood of virus transmission. Single cell analysis of these different cell types with both human and avian IAV strains will allow us to explore how virus strain and cell type influences viral diversity. Drop-based microfluidics is a method in which the host cell and virus are compartmentalized within picoliter- sized drops, creating millions of micro-environments, allowing for high-throughput analysis. Drop-based microfluidics therefore provides an ideal platform for the study of viral genetic diversity from fast evolving RNA viruses in the laboratory. Our long-term objective is to understand the evolution of IAV that leads to host adaptation, virulence, transmission, and ultimately zoonotic spread. To begin to address this long-term objective we will evaluate single cell IAV genomic heterogeneity by 1.) quantifying the genetic diversity arising from avian and seasonal human IAV infections of individual human primary cells and 2.) performing evolutionary studies by serial passaging IAV viruses at a single cell level. These two independent, but complementary aims are directed at understanding: (Aim 1) how specific cell types impact viral genetic diversity and zoonotic risk, and (Aim 2) how viral diversity evolves when system and population level bottlenecks are altered. The proposed research will broadly impact the field of single cell virology by characterizing the role that viral diversity plays in virus propagation, transmission, and evolution. These studies will yield fundamental mechanistic insights into virus-host cell dynamics, which may aid in developing efficacious vaccines and therapeutics that can target rapidly evolving IAV and other RNA viruses.