成年恒河猴对严重急性呼吸系统综合征冠状病毒2型感染的年龄依赖性反应进行解剖。

Stephanie N Langel, Carolina Garrido, Caroline Phan, Tatianna Travieso, Helene Kirshner, Todd DeMarco, Zhong-Min Ma, J Rachel Reader, Katherine J Olstad, Rebecca L Sammak, Yashavanth Shaan Lakshmanappa, Jamin W Roh, Jennifer Watanabe, Jodie Usachenko, Ramya Immareddy, Rachel Pollard, Smita S Iyer, Sallie Permar, Lisa A Miller, Koen K A Van Rompay, Maria Blasi
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引用次数: 1

摘要

严重急性呼吸综合征冠状病毒2(SARS-CoV-2)及其相关冠状病毒疾病(新冠肺炎)的全球传播导致了一场规模空前的大流行。这种感染的一个有趣特征是大多数儿童的最小疾病,这一人群患其他呼吸道病毒性疾病的风险更高。为了研究严重急性呼吸系统综合征冠状病毒2型发病机制的年龄依赖性影响,我们为两对恒河猴-猴-坝婴儿接种了严重急性呼吸系综合征冠状病毒-2型疫苗,并对呼吸道进行了病毒学和转录组学分析,评估了系统细胞因子和抗体反应。所有取样粘膜分泌物中的病毒RNA水平在呼吸道中的母婴对之间具有可比性。尽管病毒载量相当,但成年猕猴在感染后第1天的血清中显示出较高的IL-6,而CXCL10在所有动物中都被诱导。两组都出现了中和抗体反应,婴儿在第7天表现出更快的诱导。对感染后第14天分离的气管气道细胞的转录组分析显示,与成人相比,婴儿体内多种IFN刺激的基因显著上调。相反,与婴儿相比,成人诱导了与纤毛结构和功能、细胞外基质组成和代谢、凝血、血管生成和缺氧相关的基因的促纤维化转录组学特征。我们在恒河猴-猴-坝婴儿对中的研究表明,对严重急性呼吸系统综合征冠状病毒2型感染的气道差异反应取决于年龄,并描述了一种可用于研究婴儿和成人之间严重急性呼吸系统冠状病毒2型发病机制的模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dam-Infant Rhesus Macaque Pairs to Dissect Age-Dependent Responses to SARS-CoV-2 Infection.

The global spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and its associated coronavirus disease (COVID-19) has led to a pandemic of unprecedented scale. An intriguing feature of the infection is the minimal disease in most children, a demographic at higher risk for other respiratory viral diseases. To investigate age-dependent effects of SARS-CoV-2 pathogenesis, we inoculated two rhesus macaque monkey dam-infant pairs with SARS-CoV-2 and conducted virological and transcriptomic analyses of the respiratory tract and evaluated systemic cytokine and Ab responses. Viral RNA levels in all sampled mucosal secretions were comparable across dam-infant pairs in the respiratory tract. Despite comparable viral loads, adult macaques showed higher IL-6 in serum at day 1 postinfection whereas CXCL10 was induced in all animals. Both groups mounted neutralizing Ab responses, with infants showing a more rapid induction at day 7. Transcriptome analysis of tracheal airway cells isolated at day 14 postinfection revealed significant upregulation of multiple IFN-stimulated genes in infants compared with adults. In contrast, a profibrotic transcriptomic signature with genes associated with cilia structure and function, extracellular matrix composition and metabolism, coagulation, angiogenesis, and hypoxia was induced in adults compared with infants. Our study in rhesus macaque monkey dam-infant pairs suggests age-dependent differential airway responses to SARS-CoV-2 infection and describes a model that can be used to investigate SARS-CoV-2 pathogenesis between infants and adults.

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