Belser Jessica A, Gustin Kortney M, Katz Jacqueline M, Maines Taronna R, Tumpey Terrence M
Influenza Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Influenza Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA
J Virol. 2014 Sep 1;88(17):9647-54. doi: 10.1128/JVI.01067-14. Epub 2014 Jun 11.
Respiratory pathogens have traditionally been studied by examining the exposure and infection of respiratory tract tissues. However, these studies typically overlook the role of ocular surfaces, which represent both a potential site of virus replication and a portal of entry for the establishment of a respiratory infection. To model transocular virus entry in a mammalian species, we established a novel inoculation method that delivers an aerosol inoculum exclusively to the ferret ocular surface. Using influenza virus as a representative respiratory pathogen, we found that both human and avian viruses mounted productive respiratory infections in ferrets following ocular-only aerosol inoculation, and we demonstrated that H5N1 virus can result in a fatal infection at doses below 10 PFU or with exposure times as short as 2 min. Ferrets inoculated by the ocular aerosol route with an avian (H7N7, H7N9) or human (H1N1, H3N2v) virus were capable of transmitting the virus to naïve animals in direct-contact or respiratory-droplet models, respectively. Our results reveal that ocular-only exposure to virus-containing aerosols constitutes a valid exposure route for a potentially fatal respiratory infection, even for viruses that do not demonstrate an ocular tropism, underscoring the public health implications of ocular exposure in clinical or occupational settings.
In the absence of eye protection, the human ocular surface remains vulnerable to infection with aerosolized respiratory viruses. In this study, we present a way to inoculate laboratory mammals that excludes respiratory exposure, infecting ferrets only by ocular exposure to influenza virus-containing aerosols. This study demonstrates that the use of respiratory protection alone does not fully protect against influenza virus exposure, infection, and severe disease.
传统上,呼吸道病原体是通过检查呼吸道组织的暴露和感染情况来进行研究的。然而,这些研究通常忽略了眼表的作用,眼表既是病毒复制的潜在部位,也是呼吸道感染建立的入口。为了在哺乳动物物种中模拟经眼病毒进入,我们建立了一种新型接种方法,该方法仅将气溶胶接种物递送至雪貂眼表。以流感病毒作为代表性呼吸道病原体,我们发现,在仅经眼气溶胶接种后,人类和禽流感病毒均可在雪貂中引发有效的呼吸道感染,并且我们证明,H5N1病毒在低于10个空斑形成单位(PFU)的剂量下或暴露时间短至2分钟时即可导致致命感染。经眼气溶胶途径接种禽流感病毒(H7N7、H7N9)或人流感病毒(H1N1、H3N2v)的雪貂,能够分别在直接接触或呼吸道飞沫模型中将病毒传播给未感染的动物。我们的结果表明,仅通过眼部接触含病毒气溶胶就构成了导致潜在致命呼吸道感染的有效暴露途径,即使对于那些不显示嗜眼性的病毒也是如此,这突出了在临床或职业环境中眼部暴露对公共卫生的影响。
在没有眼部防护的情况下,人类眼表仍然容易受到雾化呼吸道病毒的感染。在本研究中,我们提出了一种接种实验哺乳动物的方法,该方法排除了呼吸道暴露,仅通过眼部接触含流感病毒的气溶胶感染雪貂。这项研究表明,仅使用呼吸道防护并不能完全预防流感病毒的暴露、感染和严重疾病。