Transcriptomic analyses reveal new genes and networks response to H5N1 influenza viruses in duck(Anas platyrhynchos)

被引:0
作者
HUANG Yin-hua [1 ]
FENG Hua-peng [2 ]
HUANG Li-ren [2 ]
YI Kang [3 ]
RONG En-guang [1 ]
CHEN Xiao-yun [4 ]
LI Jian-wen [3 ]
WANG Zeng [2 ]
ZHU Peng-yang [2 ]
LIU Xiao-juan [1 ]
WANG Xiao-xue [1 ]
HU Jia-xiang [1 ]
LIU Xin [3 ]
CHEN Hua-lan [2 ]
WANG Jun [3 ]
LI Ning [1 ]
机构
[1] State Key Laboratory for Agrobiotechnology,China Agricultural University
[2] State Key Laboratory of Veterinary Biotechnology,Harbin Veterinary Research Institute,Chinese Academy of Agricultural Sciences
[3] BGI-Shenzhen
[4] China Veterinary Culture Collection Center,China Institute of Veterinary Drug Control
基金
中央高校基本科研业务费专项资金资助; 中国国家自然科学基金;
关键词
duck; innate immune genes; H5N1 influenza viruses; transcriptomes;
D O I
暂无
中图分类号
S858.32 [鸭];
学科分类号
0906 ;
摘要
H5N1 influenza represents one of the great challenges to public health. Some H5N1 viruses(i.e., A/goose/Hubei/65/05, GS/65) are weakly pathogenic, while the others(i.e., A/duck/Hubei/49/05, DK/49) are highly pathogenic to their natural hosts. Here, we performed brain and spleen transcriptomic analyses of control ducks and ones infected by the DK/49 or the GS/65 H5N1 virus. We demonstrated that, compared to the GS/65 virus, the DK/49 virus infection changed more numerous immune genes’ expression and caused continuous increasing of immune pathways(i.e., RIG-I and MDA5) in ducks. We found that both H5N1 virus strains might escape or subvert host immune response through affecting alternative translation of immune genes, while the DK/49 virus seemed to induce alternative translation of more immune genes than the GS/65 virus. We also identified five co-expressional modules associated with H5N1 virus replication through the weight correlation network analysis(WGCNA). Moreover, we first demonstrated that the duck BCL2 L15 and DCSTAMP in one of these five modules inhibited both the highly pathogenic and weakly pathogenic H5N1 virus replication efficiently. These analyses, in combination with our comprehensive transcriptomic data, provided global view of the molecular architecture for the interaction between host and H5N1 viruses.
引用
收藏
页码:1460 / 1472
页数:13
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