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Immune Responses of Ducks Infected with Duck Tembusu Virus

Overview
Journal Front Microbiol
Specialty Microbiology
Date 2015 May 26
PMID 26005441
Citations 34
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Abstract

Duck Tembusu virus (DTMUV) can cause serious disease in ducks, characterized by reduced egg production. Although the virus has been isolated and detection methods developed, the host immune responses to DTMUV infection are unclear. Therefore, we systematically examined the expression of immune-related genes and the viral distribution in DTMUV-infected ducks, using quantitative real-time PCR. Our results show that DTMUV replicates quickly in many tissues early in infection, with the highest viral titers in the spleen 1 day after infection. Rig-1, Mda5, and Tlr3 are involved in the host immune response to DTMUV, and the expression of proinflammatory cytokines (Il-1β, -2, -6, Cxcl8) and antiviral proteins (Mx, Oas, etc.) are also upregulated early in infection. The expression of Il-6 increased most significantly in the tissues tested. The upregulation of Mhc-I was observed in the brain and spleen, but the expression of Mhc-II was upregulated in the brain and downregulated in the spleen. The expression of the interferons was also upregulated to different degrees in the spleen but that of the brain was various. Our study suggests that DTMUV replicates rapidly in various tissues and that the host immune responses are activated early in infection. However, the overexpression of cytokines may damage the host. These results extend our understanding of the immune responses of ducks to DTMUV infection, and provide insight into the pathogenesis of DTMUV attributable to host factors.

Citing Articles

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Chen J, Yang F, Lai L, Li H, Pan C, Bao X Viruses. 2025; 16(12.

PMID: 39772141 PMC: 11680370. DOI: 10.3390/v16121831.


Pathogenicity of Duck Adenovirus Type 3 in Chickens.

Zhang X, Xu B, Zhou H, Zhou X, Wang Q, Sun J Animals (Basel). 2024; 14(16).

PMID: 39199818 PMC: 11350851. DOI: 10.3390/ani14162284.


Advancements in Research on Duck Tembusu Virus Infections.

Cheng Y, Wang R, Wu Q, Chen J, Wang A, Wu Z Viruses. 2024; 16(5).

PMID: 38793692 PMC: 11126125. DOI: 10.3390/v16050811.


Duck LGP2 Downregulates RIG-I Signaling Pathway-Mediated Innate Immunity Against Tembusu Virus.

Li T, Ren Y, Zhang T, Zhai X, Wang X, Wang J Front Immunol. 2022; 13:916350.

PMID: 35784309 PMC: 9241487. DOI: 10.3389/fimmu.2022.916350.


RNA-Seq analysis of duck embryo fibroblast cells gene expression during duck Tembusu virus infection.

Pan Y, Wu X, Cai W, Cheng A, Wang M, Chen S Vet Res. 2022; 53(1):34.

PMID: 35585616 PMC: 9116716. DOI: 10.1186/s13567-022-01051-y.


References
1.
Pichlmair A, Reis e Sousa C . Innate recognition of viruses. Immunity. 2007; 27(3):370-83. DOI: 10.1016/j.immuni.2007.08.012. View

2.
Quicke K, Suthar M . The innate immune playbook for restricting West Nile virus infection. Viruses. 2013; 5(11):2643-58. PMC: 3856407. DOI: 10.3390/v5112643. View

3.
Jiang T, Liu J, Deng Y, Su J, Xu L, Liu Z . Development of RT-LAMP and real-time RT-PCR assays for the rapid detection of the new duck Tembusu-like BYD virus. Arch Virol. 2012; 157(12):2273-80. DOI: 10.1007/s00705-012-1431-7. View

4.
Tsai Y, Chang S, Lee C, Kao C . Human TLR3 recognizes dengue virus and modulates viral replication in vitro. Cell Microbiol. 2009; 11(4):604-15. DOI: 10.1111/j.1462-5822.2008.01277.x. View

5.
Fredericksen B, Gale Jr M . West Nile virus evades activation of interferon regulatory factor 3 through RIG-I-dependent and -independent pathways without antagonizing host defense signaling. J Virol. 2006; 80(6):2913-23. PMC: 1395472. DOI: 10.1128/JVI.80.6.2913-2923.2006. View