共 59 条
Host Genetic Background Strongly Influences the Response to Influenza A Virus Infections
被引:164
作者:
Srivastava, Barkha
[1
,2
]
Blazejewska, Paulina
[1
,2
]
Hessmann, Manuela
[1
,2
]
Bruder, Dunja
[3
]
Geffers, Robert
[4
]
Mauel, Susanne
[5
]
Gruber, Achim D.
[5
]
Schughart, Klaus
[1
,2
]
机构:
[1] Helmholtz Ctr Infect Res, Dept Expt Mouse Genet, Braunschweig, Germany
[2] Univ Vet Med Hannover, Braunschweig, Germany
[3] Helmholtz Ctr Infect Res, Res Grp Immunoregulat, Braunschweig, Germany
[4] Helmholtz Ctr Infect Res, Dept Cell Biol, Braunschweig, Germany
[5] Free Univ Berlin, Fac Vet Med, Dept Vet Pathol, D-1000 Berlin, Germany
来源:
PLOS ONE
|
2009年
/
4卷
/
03期
关键词:
D O I:
10.1371/journal.pone.0004857
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:
The genetic make-up of the host has a major influence on its response to combat pathogens. For influenza A virus, several single gene mutations have been described which contribute to survival, the immune response and clearance of the pathogen by the host organism. Here, we have studied the influence of the genetic background to influenza A H1N1 (PR8) and H7N7 (SC35M) viruses. The seven inbred laboratory strains of mice analyzed exhibited different weight loss kinetics and survival rates after infection with PR8. Two strains in particular, DBA/2J and A/J, showed very high susceptibility to viral infections compared to all other strains. The LD50 to the influenza virus PR8 in DBA/2J mice was more than 1000-fold lower than in C57BL/6J mice. High susceptibility in DBA/2J mice was also observed after infection with influenza strain SC35M. In addition, infected DBA/2J mice showed a higher viral load in their lungs, elevated expression of cytokines and chemokines, and a more severe and extended lung pathology compared to infected C57BL/6J mice. These findings indicate a major contribution of the genetic background of the host to influenza A virus infections. The overall response in highly susceptible DBA/2J mice resembled the pathology described for infections with the highly virulent influenza H1N1-1918 and newly emerged H5N1 viruses.
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