基因型
生物
病毒学
呼吸道
H5N1亚型流感病毒
气道
病毒
呼吸上皮
人流感
呼吸系统
甲型流感病毒
类有机物
免疫学
呼吸道感染
鼻子
上皮
病毒释放
正粘病毒科
效价
禽流感病毒
大流行
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
血凝素(流感)
微生物学
作者
Xiaojuan Zhang,Stephanie Joy-Ann Lam,Lin-Lei Chen,Carol Ho-Yan Fong,Wan Mui Chan,Jonathan Daniel Ip,Deng Shaofeng,Siwen Liu,Rachel Chun Yee Tam,Pui Wang,Kwok-Hung Chan,King‐Pui Florence Chan,James Chung Man Ho,Jie Zhou,Kwok-Yung Yuen,Honglin Chen,Kelvin Kai-Wang To
标识
DOI:10.1093/infdis/jiaf598
摘要
Abstract Three critically ill or fatal avian influenza A(H5N1) human infections have been reported in North America since November 2024. Notably, all were infected with genotype D1.1 instead of B3.13, the dominant genotype before November 2024. Here, we demonstrated that D1.1 could replicate to higher titers in human nasal and airway organoid-derived transwell monolayers from 6 donors. D1.1 exhibited a better binding to α2,3- and α2,6-linked SA than B3.13. No significant differences in most inflammatory or antiviral cytokines/chemokines was observed. These observations suggest that D1.1 is better adapted to both the upper and lower human respiratory tract epithelium than B3.13.
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