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Histone modifications induced by MDV infection at early cytolytic and latency phases
Authors:Apratim Mitra  Juan Luo  Yanghua He  Yulan Gu  Huanmin Zhang  Keji Zhao  Kairong Cui  Jiuzhou Song
Affiliation:1.Department of Animal & Avian Sciences,University of Maryland,College Park,USA;2.USDA, ARS,Avian Disease and Oncology Laboratory,East Lansing,USA;3.Systems Biology Center,National Heart, Lung and Blood Institute, National Institutes of Health,Bethesda,USA;4.Department of Animal Breeding and Genetics,College of Animal Sciences, China Agricultural University,Beijing,P.R. China
Abstract:

Background

Marek’s disease (MD) is a highly contagious, lymphomatous disease of chickens induced by a herpesvirus, Marek’s disease virus (MDV) that is the cause of major annual losses to the poultry industry. MD pathogenesis involves multiple stages including an early cytolytic phase and latency, and transitions between these stages are governed by several host and environmental factors. The success of vaccination strategies has led to the increased virulence of MDV and selective breeding of naturally resistant chickens is seen as a viable alternative. While multiple gene expression studies have been performed in resistant and susceptible populations, little is known about the epigenetic effects of infection.

Results

In this study, we investigated temporal chromatin signatures induced by MDV by analyzing early cytolytic and latent phases of infection in the bursa of Fabricius of MD-resistant and –susceptible birds. Major global variations in chromatin marks were observed at different stages of MD in the two lines. Differential H3K27me3 marks were associated with immune-related pathways, such as MAP kinase signaling, focal adhesion and neuroactive ligand receptor interaction, and suggested varying degrees of silencing in response to infection. Immune-related microRNAs, e.g. gga-miR-155 and gga-miR-10b, bore chromatin signatures, which suggested their contribution to MD-susceptibility. Finally, several members of the focal adhesion pathway, e.g. THBS4 and ITGA1, showed marked concordance between gene expression and chromatin marks indicating putative epigenetic regulation in response to MDV infection.

Conclusion

Our comprehensive analysis of chromatin signatures, therefore, revealed further clues about the epigenetic effects of MDV infection although further studies are necessary to elucidate the functional implications of the observed variations in histone modifications.
Keywords:
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