Evolution of H3N2 Influenza Virus in a Guinea Pig Model

被引:19
作者
Long, Jinxue [1 ]
Bushnell, Ruth V. [1 ]
Tobin, John K. [1 ]
Pan, Keyao [2 ]
Deem, Michael W. [2 ]
Nara, Peter L. [1 ,3 ]
Tobin, Gregory J. [1 ,3 ]
机构
[1] Biol Mimet Inc, Frederick, MD USA
[2] Rice Univ, Dept Bioengn & Phys & Astron, Houston, TX USA
[3] Iowa State Univ, Coll Vet Med, Dept Biol Sci, Ames, IA USA
来源
PLOS ONE | 2011年 / 6卷 / 07期
关键词
A VIRUS; TRANSMISSION MODEL; ANTIGENIC DISTANCE; VACCINE DESIGN; HEMAGGLUTININ; GLYCOSYLATION; EPITOPE; NEUTRALIZATION; MECHANISMS; SELECTION;
D O I
10.1371/journal.pone.0020130
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Studies of influenza virus evolution under controlled experimental conditions can provide a better understanding of the consequences of evolutionary processes with and without immunological pressure. Characterization of evolved strains assists in the development of predictive algorithms for both the selection of subtypes represented in the seasonal influenza vaccine and the design of novel immune refocused vaccines. To obtain data on the evolution of influenza in a controlled setting, naive and immunized Guinea pigs were infected with influenza A/Wyoming/2003 (H3N2). Virus progeny from nasal wash samples were assessed for variation in the dominant and other epitopes by sequencing the hemagglutinin (HA) gene to quantify evolutionary changes. Viral RNA from the nasal washes from infection of naive and immune animals contained 6% and 24.5% HA variant sequences, respectively. Analysis of mutations relative to antigenic epitopes indicated that adaptive immunity played a key role in virus evolution. HA mutations in immunized animals were associated with loss of glycosylation and changes in charge and hydrophobicity in and near residues within known epitopes. Four regions of HA-1 (75-85, 125-135, 165-170, 225-230) contained residues of highest variability. These sites are adjacent to or within known epitopes and appear to play an important role in antigenic variation. Recognition of the role of these sites during evolution will lead to a better understanding of the nature of evolution which help in the prediction of future strains for selection of seasonal vaccines and the design of novel vaccines intended to stimulated broadened cross-reactive protection to conserved sites outside of dominant epitopes.
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页数:9
相关论文
共 42 条
[1]   Loss of the N-linked glycan at residue 173 of human parainfluenza virus type 1 hemagglutinin-neuraminidase exposes a second receptor-binding site [J].
Alymova, Irina V. ;
Taylor, Garry ;
Mishin, Vasiliy P. ;
Watanabe, Makiko ;
Murti, K. Gopal ;
Boyd, Kelli ;
Chand, Pooran ;
Babu, Y. Sudhakara ;
Portner, Allen .
JOURNAL OF VIROLOGY, 2008, 82 (17) :8400-8410
[2]  
[Anonymous], 2003, Wkly Epidemiol Rec, V78, P77
[3]   PROPORTION OF REVERTANT AND MUTANT PHAGE IN A GROWING POPULATION, AS A FUNCTION OF MUTATION AND GROWTH-RATE [J].
BATSCHELET, E ;
DOMINGO, E ;
WEISSMANN, C .
GENE, 1976, 1 (01) :27-32
[4]   Oseltamivir-Resistant Influenza A Viruses Are Transmitted Efficiently among Guinea Pigs by Direct Contact but Not by Aerosol [J].
Bouvier, Nicole M. ;
Lowen, Anice C. ;
Palese, Peter .
JOURNAL OF VIROLOGY, 2008, 82 (20) :10052-10058
[5]  
Brammer L., 2008, Morbidity and Mortality Weekly Report, V57, P179
[6]   Serological characterization of guinea pigs infected with H3N2 human influenza or immunized with hemagglutinin protein [J].
Bushnell, Ruth V. ;
Tobin, John K. ;
Long, Jinxue ;
Schultz-Cherry, Stacey ;
Chaudhuri, A. Ray ;
Nara, Peter L. ;
Tobin, Gregory J. .
VIROLOGY JOURNAL, 2010, 7
[8]   Evolvability is a selectable trait [J].
Earl, DJ ;
Deem, MW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (32) :11531-11536
[9]   Antibody Recognition of a Highly Conserved Influenza Virus Epitope [J].
Ekiert, Damian C. ;
Bhabha, Gira ;
Elsliger, Marc-Andre ;
Friesen, Robert H. E. ;
Jongeneelen, Mandy ;
Throsby, Mark ;
Goudsmit, Jaap ;
Wilson, Ian A. .
SCIENCE, 2009, 324 (5924) :246-251
[10]   Antigen distortion allows influenza virus to escape neutralization [J].
Fleury, D ;
Wharton, SA ;
Skehel, JJ ;
Knossow, M ;
Bizebard, T .
NATURE STRUCTURAL BIOLOGY, 1998, 5 (02) :119-123