Tropism for ciliated cells is the dominant driver of influenza viral burst size in the human airway

• 成果类型: Article
• 署名作者: Roach, Shanley N.; Shepherd, Frances K.; Mickelson, Clayton K.; Fiege, Jessica K.; Thielen, Beth K.; Pross, Lauren M.; Sanders, Autumn E.; Mitchell, Jason S.; Robertson, Mason; Fife, Brian T.; Langlois, Ryan A.
• 署名单位: University of Minnesota System; University of Minnesota Twin Cities; University of Minnesota System; University of Minnesota Twin Cities; University of Minnesota System; University of Minnesota Twin Cities; University of Minnesota System; University of Minnesota Twin Cities
• 刊物名称: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
• ISSN/ISSBN: 0027-8839
• DOI: 10.1073/pnas.2320303121
• 发表日期: 2024-07-30
• 关键词: virus; differentiation

摘要

Influenza viruses pose a significant burden on global human health. Influenza has a broad cellular tropism in the airway, but how infection of different epithelial cell types impacts replication kinetics and burden in the airways is not fully understood. Using primary human airway cultures, which recapitulate the diverse epithelial cell landscape of the human airways, we investigated the impact of cell type composition on virus tropism and replication kinetics. Cultures were highly diverse across multiple donors and 30 independent differentiation conditions and supported a range of influenza replication. Although many cell types were susceptible to influenza, ciliated and secretory cells were predominantly infected. Despite the strong tropism preference for secretory and ciliated cells, which consistently make up 75% or more of infected cells, only ciliated cells were associated with increased virus production. Surprisingly, infected secretory cells were associated with overall reduced virus output. The disparate response and contribution to influenza virus production could be due to different pro- and antiviral interferon- stimulated gene signatures between ciliated and secretory populations, which were interrogated with single- cell RNA sequencing. These data highlight the heterogeneous outcomes of influenza virus infections in the complex cellular environment of the human airway and the disparate impacts of infected cell identity on multiround burst size, even among preferentially infected cell types.