Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, United States of America.
Division of Infectious Diseases, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, United States of America.
PLoS Pathog. 2021 Feb 18;17(2):e1009273. doi: 10.1371/journal.ppat.1009273. eCollection 2021 Feb.
Human-to-human transmission of influenza viruses is a serious public health threat, yet the precise role of immunity from previous infections on the susceptibility to airborne infection is still unknown. Using the ferret model, we examined the roles of exposure duration and heterosubtypic immunity on influenza transmission. We demonstrate that a 48 hour exposure is sufficient for efficient transmission of H1N1 and H3N2 viruses. To test pre-existing immunity, a gap of 8-12 weeks between primary and secondary infections was imposed to reduce innate responses and ensure robust infection of donor animals with heterosubtypic viruses. We found that pre-existing H3N2 immunity did not significantly block transmission of the 2009 H1N1pandemic (H1N1pdm09) virus to immune animals. Surprisingly, airborne transmission of seasonal H3N2 influenza strains was abrogated in recipient animals with H1N1pdm09 pre-existing immunity. This protection from natural infection with H3N2 virus was independent of neutralizing antibodies. Pre-existing immunity with influenza B virus did not block H3N2 virus transmission, indicating that the protection was likely driven by the adaptive immune response. We demonstrate that pre-existing immunity can impact susceptibility to heterologous influenza virus strains, and implicate a novel correlate of protection that can limit the spread of respiratory pathogens through the air.
人际传播流感病毒是一个严重的公共卫生威胁,但先前感染产生的免疫力对空气传播感染的易感性的确切作用仍不清楚。我们使用雪貂模型研究了暴露持续时间和异源型免疫在流感传播中的作用。我们证明,48 小时的暴露足以有效传播 H1N1 和 H3N2 病毒。为了测试预先存在的免疫,在初次感染和二次感染之间设置 8-12 周的间隔,以减少先天反应并确保供体动物对异源型病毒进行强有力的感染。我们发现,预先存在的 H3N2 免疫并不能显著阻止 2009 年 H1N1 大流行(H1N1pdm09)病毒向免疫动物的传播。令人惊讶的是,具有 H1N1pdm09 预先存在免疫的接受者动物中,季节性 H3N2 流感株的空气传播被阻断。这种对自然感染 H3N2 病毒的保护作用不依赖于中和抗体。具有流感 B 病毒的预先存在免疫并不能阻止 H3N2 病毒的传播,表明这种保护作用可能是由适应性免疫反应驱动的。我们证明,预先存在的免疫可以影响对异源流感病毒株的易感性,并暗示了一种新的保护相关性,可以限制呼吸道病原体通过空气传播。