scholarly journals Type I Interferon Response in Calves Experimentally Infected with Bovine Viral Diarrhea Virus Type 1b and Mannheimia Haemolytica

Author(s):  
Gifford CA
2008 ◽  
Vol 132 (1-2) ◽  
pp. 49-58 ◽  
Author(s):  
Natalia P. Smirnova ◽  
Helle Bielefeldt-Ohmann ◽  
Hana Van Campen ◽  
Kathleen J. Austin ◽  
Hyungchul Han ◽  
...  

2009 ◽  
Vol 29 (1) ◽  
pp. 23-36 ◽  
Author(s):  
Megan L. Shoemaker ◽  
Natalia P. Smirnova ◽  
Helle Bielefeldt-Ohmann ◽  
Kathleen J. Austin ◽  
Alberto van Olphen ◽  
...  

2020 ◽  
Vol 278 ◽  
pp. 197862 ◽  
Author(s):  
Sara M. Nilson ◽  
Aspen M. Workman ◽  
David Sjeklocha ◽  
Bruce Brodersen ◽  
Dale M. Grotelueschen ◽  
...  

2019 ◽  
Author(s):  
Yanhua HE ◽  
Yajun YANG ◽  
Xin HUANG ◽  
Yunfen ZHANG ◽  
Chencheng XIAO ◽  
...  

Abstract Background: Monocytes are significant players in the detection of invading pathogens, particularly in pathogen defense. Bovine Viral Diarrhea Virus (BVDV) can cause a persistent infection and immune suppression if animals are infected with an non-cytopathic (ncp) biotype. However, its exact role in ncp BVDV-infected bovine monocytes remains poorly understood. To explore the immune suppression mechanisms of ncp BVDV, we used a transcriptomics approach to find genes with differential expression patterns in monocytes during infection with ncp BVDV over time. Results: Bovine monocytes were sampled at 2 and 24 h post-infection (hpi) to represent the early and late stages of an ncp biotype strain of bovine viral diarrhea virus infection. Compared with the non-infected cells, 9959 and 7977 differentially expressed gene (DEGs) were identified at 2 and 24 h hpi, respectively. These DEGs were associated with signal transduction, immune response, apoptotic process, cellular process , binding and cellular component. The differential expression profiles of select the type I interferon signaling pathway , interferon (IFN)-stimulated genes (ISGs), and genes involved in the innate immune response, including IRF7, DDX3X, TLR13, DDX58(RIG-I), MVAS, TLR9, TRAF6, IRF1, IFIT1, STAT1, ISG20, TRIM25, MX1,NLRX1, CYLD, SIKE1 and ZAP70 were confirmed by real-time quantitative PCR and consistent with the RNA-seq data. These results indicated that infection with ncp BVDV could activate type I interferon signaling pathway in bovine monocytes and induces weak ISGs responses, which extends our present understanding how the virus modulates the immune response and leads to better understanding behind the immunopathogenesis of ncp BVDV. Conclusion: Our transciptome anslysis provides useful initial data towards better understanding of the infection mechanisms used by ncp BVDV, while highlighting the potential molecular relationships occurring between the virus and the host’s immune response.


2006 ◽  
Vol 80 (23) ◽  
pp. 11723-11732 ◽  
Author(s):  
Louise Hilton ◽  
Kartykayan Moganeradj ◽  
Gang Zhang ◽  
Yun-Hsiang Chen ◽  
Richard E. Randall ◽  
...  

ABSTRACT Bovine viral diarrhea virus (BVDV) is a pestivirus that can establish a persistent infection in the developing fetus and has the ability to disable the production of type I interferon. In this report, we extend our previous observations that BVDV encodes a protein able to specifically block the activity of interferon regulatory factor 3 (IRF-3), a transcription factor essential for interferon promoter activation, by demonstrating that this is a property of the N-terminal protease fragment (NPro) of the BVDV polyprotein. Although BVDV infections cause relocalization of cellular IRF-3 from the cytoplasm to the nucleus early in infection, NPro blocks IRF-3 from binding to DNA. NPro has the additional property of targeting IRF-3 for polyubiquitination and subsequent destruction by cellular multicatalytic proteasomes. The autoprotease activity of NPro is not required for the inhibition of type I interferon induction or the targeting of IRF-3 for degradation.


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