Altered Receptor Specificity and Cell Tropism of D222G Hemagglutinin Mutants Isolated from Fatal Cases of Pandemic A(H1N1) 2009 Influenza Virus

被引:163
作者
Liu, Yan [5 ]
Childs, Robert A. [5 ]
Matrosovich, Tatyana [1 ]
Wharton, Stephen [2 ]
Palma, Angelina S. [3 ]
Chai, Wengang [5 ]
Daniels, Rodney [2 ]
Gregory, Victoria [2 ]
Uhlendorff, Jennifer [1 ]
Kiso, Makoto [4 ]
Klenk, Hans-Dieter [1 ]
Hay, Alan
Feizi, Ten [5 ]
Matrosovich, Mikhail [1 ]
机构
[1] Univ Marburg, Inst Virol, D-35043 Marburg, Germany
[2] Natl Inst Med Res, MRC, Div Virol, London NW7 1AA, England
[3] Univ Nova Lisboa, Fac Ciencias & Tecnol, Dept Quim, REQUIMTE,Ctr Quim Fina & Biotecnol, P-2829516 Caparica, Portugal
[4] Gifu Univ, Dept Appl Bioorgan Chem, Fac Appl Biol Sci, Gifu 50111, Japan
[5] Univ London Imperial Coll Sci Technol & Med, Glycosci Lab, Dept Med, Harrow HA1 3UJ, Middx, England
基金
英国生物技术与生命科学研究理事会; 英国医学研究理事会; 英国惠康基金; 英国工程与自然科学研究理事会;
关键词
AIRWAY EPITHELIAL-CELLS; MYCOPLASMA-PNEUMONIAE; A H1N1; BINDING PROPERTIES; SEVERE DISEASE; CARBOHYDRATE; SUBSTITUTION; MICROARRAY; INFECTION; MAMMALS;
D O I
10.1128/JVI.01639-10
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Mutations in the receptor-binding site of the hemagglutinin of pandemic influenza A(H1N1) 2009 viruses have been detected sporadically. An Asp222Gly (D222G) substitution has been associated with severe or fatal disease. Here we show that 222G variants infected a higher proportion of ciliated cells in cultures of human airway epithelium than did viruses with 222D or 222E, which targeted mainly nonciliated cells. Carbohydrate microarray analyses showed that 222G variants bind a broader range of alpha 2-3-linked sialyl receptor sequences of a type expressed on ciliated bronchial epithelial cells and on epithelia within the lung. These features of 222G mutants may contribute to exacerbation of disease.
引用
收藏
页码:12069 / 12074
页数:6
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