Virus-host interactions: from systems biology to translational research
- PMID: 19576841
- PMCID: PMC2742299
- DOI: 10.1016/j.mib.2009.06.003
Virus-host interactions: from systems biology to translational research
Abstract
Research embracing systems biology approaches and careful analysis of the critical host response has greatly expanded our understanding of infectious diseases. First-generation studies based on genomics and proteomics have made significant progress in establishing the foundation for network-based investigations on virus-host interactions. More recently, data from complementary high-throughput technologies, such as siRNA and microRNA screens and next-generation sequencing, are augmenting systems level analyses and are providing a more detailed and insightful multidimensional view of virus-host networks. Together with advances in data integration, systems biology approaches now have the potential to provide profound impacts on translational research, leading to the more rapid development of new therapeutics and vaccines for infectious diseases. In this review, we highlight new high-throughput technologies, a new philosophy for studying virus-host interactions, and discuss the potential of systems biology to facilitate bench-to-bedside research and create novel strategies to combat disease. Can we save the world using these approaches? Read on.
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- Boutros M, Ahringer J. The art and design of genetic screens: RNA interference. Nature Reviews Genetics. 2008;9:554–566. - PubMed
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[10] Brass et al. (*) – The authors were the first to demonstrate the importance of siRNA genomic screens in identifying host cellular factors vital for HIV viral replication.
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[13] Calderwood et al. (*) – This is the first study to apply a high-throughput yeast two-hybrid approach to identify physical interaction between Epstein Barr virus and human proteins. The authors use these interactions to suggest mechanism of virulence.
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[23] Mortazavi et al (**) – This is the first study to apply next-generation sequencing technology to analyze mammalian transcriptome. This study reported wide linear range of transcript detection, and the detection of alternate splice isoforms and novel transcripts.
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[30] Zhang et al. (*) – The authors reported a multi-scale agent-based computational model to simulate cancer heterogeneity. The model integrates a simplified epidermal growth factor receptor gene-protein network coupled with a cell cycle module.
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- R01HL080621/HL/NHLBI NIH HHS/United States
- P51RR000166/RR/NCRR NIH HHS/United States
- P01AI058113/AI/NIAID NIH HHS/United States
- P51 RR000166/RR/NCRR NIH HHS/United States
- R24 OD011157/OD/NIH HHS/United States
- R01AI022646/AI/NIAID NIH HHS/United States
- P30 DA015625/DA/NIDA NIH HHS/United States
- R01 AI022646/AI/NIAID NIH HHS/United States
- R24RR016354/RR/NCRR NIH HHS/United States
- R01 HL080621/HL/NHLBI NIH HHS/United States
- R24 RR016354/RR/NCRR NIH HHS/United States
- P30DA015625/DA/NIDA NIH HHS/United States
- P01 AI058113/AI/NIAID NIH HHS/United States
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