Changes in the hemagglutinin of H5N1 viruses during human infection - Influence on receptor binding

被引:28
作者
Crusat, Martin [1 ,2 ]
Liu, Junfeng [3 ]
Palma, Angelina S. [4 ,5 ]
Childs, Robert A. [4 ]
Liu, Yan [4 ]
Wharton, Stephen A. [3 ]
Lin, Yi Pu [3 ]
Coombs, Peter J. [3 ]
Martin, Stephen R. [3 ]
Matrosovich, Mikhail [6 ]
Chen, Zi [3 ]
Stevens, David J. [3 ]
Vo Minh Hien [7 ]
Tran Tan Thanh [1 ]
Le Nguyen Truc Nhu [1 ]
Lam Anh Nguyet [7 ]
Do Quang Ha [1 ]
van Doorn, H. Rogier [1 ]
Tran Tinh Hien [7 ]
Conradt, Harald S. [8 ]
Kiso, Makoto [9 ]
Gamblin, Steve J. [3 ]
Chai, Wengang [4 ]
Skehel, John J. [3 ]
Hay, Alan J. [3 ]
Farrar, Jeremy [1 ,10 ]
de Jong, Menno D. [1 ,2 ]
Feizi, Ten [4 ]
机构
[1] Univ Oxford, Clin Res Unit, Hosp Trop Dis, Ho Chi Minh City, Vietnam
[2] Univ Amsterdam, Acad Med Ctr, Dept Med Microbiol, NL-1105 AZ Amsterdam, Netherlands
[3] MRC Natl Inst Med Res, London, England
[4] Imperial Coll London, Dept Med, Glycosci Lab, London, England
[5] Univ Nova Lisboa, Fac Sci & Technol, REQUIMTE CQFB, Caparica, Portugal
[6] Univ Marburg, Inst Virol, D-35032 Marburg, Germany
[7] Hosp Trop Dis, Ho Chi Minh City, Vietnam
[8] GlycoThera GmbH, Hannover, Germany
[9] Gifu Univ, Dept Appl Bioorgan Chem, Gifu, Japan
[10] Natl Univ Singapore, Singapore 117548, Singapore
基金
英国医学研究理事会; 英国惠康基金; 英国生物技术与生命科学研究理事会; 英国工程与自然科学研究理事会;
关键词
H5N1 influenza infection; Pyrosequencing; Hemagglutinin; Receptor specificity; Hemagglutination assays; Receptor binding; Carbohydrate microarray; Biolayer interferometry; Synthetic sialylglycopolymers; Hemagglutinin X-ray crystal structure; A VIRUSES; PANDEMIC INFLUENZA; CELL TROPISM; AMINO-ACID; SPECIFICITY; TRANSMISSION; MICROARRAY; ORIGIN; EVOLUTION; SELECTION;
D O I
10.1016/j.virol.2013.08.010
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
As avian influenza A(H5N1) viruses continue to circulate in Asia and Africa, global concerns of an imminent pandemic persist. Recent experimental studies suggest that efficient transmission between humans of current H5N1 viruses only requires a few genetic changes. An essential step is alteration of the virus hemagglutinin from preferential binding to avian receptors for the recognition of human receptors present in the upper airway. We have identified receptor-binding changes which emerged during H5N1 infection of humans, due to single amino acid substitutions, Ala134Val and Ile151Phe, in the hemagglutinin. Detailed biological, receptor-binding, and structural analyses revealed reduced binding of the mutated viruses to avian-like receptors, but without commensurate increased binding to the human-like receptors investigated, possibly reflecting a receptor-binding phenotype intermediate in adaptation to more human-like characteristics. These observations emphasize that evolution in nature of avian H5N1 viruses to efficient binding of human receptors is a complex multistep process. (C) 2013 The Authros. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:326 / 337
页数:12
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