a systems approach to infectious disease research: influenza
DESCRIPTION
Develop a molecular network model of the interaction between influenza virus and the innate immune system. A Systems Approach to Infectious Disease Research: Influenza. Influenza Contract Research Collaboration. Exp. Prep & Pathophysiology – St. Jude (Doherty, Thomas, Webby) - PowerPoint PPT PresentationTRANSCRIPT
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A Systems Approach to Infectious Disease Research: Influenza
Develop a molecular network model of the interaction
between influenza virus and the innate immune system.
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Influenza Contract Research Collaboration
Exp. Prep & Pathophysiology – St. Jude (Doherty, Thomas, Webby)
Genomics & Proteomics – ISB (Aderem) UW (Rubens);
Lipidomics – UCSD (Dennis, Quehenberger); Vanderbilt (Brown)
• Computation – ISB (Shmulevich/Aderem)
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Computational Core (ISB)
Genomics Core(ISB)
Proteomics Core(ISB)
Lipidomics Core A(UCSD)
Pathology(St. Jude)
Influenza infected mTECs, (St. Jude)
Influenza infected mice(ID&P Core St. Jude)
RNA frominfected mTECs
RNA -sorted cellsBAL/lung
½ BAL fluid ½ BAL fluid lung, liver, spleen
Webportal
Raw data
Iterative experimental design Analysis results
Computational Core (ISB)
Genomics Core(ISB)
Proteomics Core(ISB)
Lipidomics Core A(UCSD)
Pathology(St. Jude)
Influenza infected mTECs, (St. Jude)
Influenza infected mice(ID&P Core St. Jude)
RNA frominfected mTECs
RNA -sorted cellsBAL/lung
½ BAL fluid ½ BAL fluid lung, liver, spleen
Webportal
Raw data
Iterative experimental design Analysis results
Research Focus 1 – Workflow
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Viral Models
• PR8 (A/Puerto Rico/34)– Mouse adapted, reverse genetics virus with high
pathogenicity
• x31 (HA/NA from A/Aichi/2/68)– Mouse adapted, reverse genetics virus on PR8 backbone
with low pathogenicity
• rg/VN1203 (HA/NA from A/Vietnam/1203/04)– “Clipped” HA from high path H5N1, reverse genetics virus
on PR8 backbone with high pathogenicity (possibly higher than PR8)
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Research Focus 1 –Specific Aims
Sub-aim ATo determine the regulatory networks controlling the innate immune response to infection with influenza strains of varying pathogenicity, and to determine their contribution to resolving infection and inducing pathology.
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Identification of key transcriptional regulators
Extended transcriptional regulatory network showing differentially expressed transcription factor genes and associations with downstream interferon-responsive genes. A directed edge indicates that (1) the target gene cis-regulatory region contains one or more high-quality matches for the TF binding site motif recognized by the source gene’s product (TF), and (2) the colors of the source and target are consistent with known function (activation and/or repression) of the source TF. A TF gene was included in the diagram only if its binding site motif is enriched within cis-regulatory regions of genes whose expression levels were altered by the pathogenicity of the virus.
Orange = higher in PR8 infection than x31Green = lower in PR8 infection than x31
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Research Focus 1 –Specific Aims
Sub-aim BTo characterize the spectrum of proteins and bioactive lipid mediators induced in the lung in response to infection with influenza strains of varying virulence, and to identify those that correlate with enhanced pathogenicity.
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Profile proteins in influenza infected lungs
• MRM (peptide atlas)
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Profile eicosanoids in the lung following influenza infection
Identify novel lipids that are produced in the lung during influenza infection
Sub-aim B2 –Lipid profiling
Begins in Year 2
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Lipidomics: Levels of Mediators in a Time Course Experiment
0 8d 13dBALCD45AEC 0 6 9 11 13 19d
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Research Focus 1 –Specific Aims
Sub-aim CTo map the regulatory networks induced in epithelial cells by influenza strains of varying pathogenicity, and establish the mechanisms that create highly pathogenic phenotypes.
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Mouse tracheal epithelial cell (mTEC) culture is used as a model for epithelial cells lining the airways.
Polarized cells growing on a membrane with the apical side exposed to air.
Cells form a monolayer sealed by tight junctions.
Cells are fully differentiated, form cilia and closely resemble epithelial cells in vivo.
Sub-aim C: in vitro Infection Model (mTECs)
Insert
Plate well
Media
Apical
Basolateral
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Research Focus 1 –Specific Aims
Sub-aim D
To identify the critical determinants of pathogenicity by generating mutant viruses containing individual genetic elements of highly virulent H5N1, and assess their impact on the networks defined in Sub-aims A-C.
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“PR8” “PR8:5”“PR8:D92E”
(Point mutation in NS1) (Five amino-acid deletion in NS1)
Both of these mutations have been shown to increase virulence.
Sub-aim D: Identify Critical Determinants of Pathogenicity
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Research Focus 2- Specific Aims
Subaim A: Characterize the host proteins targeted by influenza proteins that are associated with virulence.
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Research Focus 2- Specific Aims
Subaim B: Characterize the unique lipid envelope components of pathogenic strains of influenza.
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Research Focus 2 – Viral Lipidomics
Measure lipid envelope composition from various strains infecting mTECs using mass-spectrometry approaches.
PR8 (H1N1)
x31 (H3N2)
rgVN1203 (H5N1)
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Sub-aim A: Determine the S. aureus transcriptional regulatory networks induced during superinfection following influenza infection.
Research Focus 3 - Specific Aims
Sub-aim B: Determine the innate immune regulatory networks induced during superinfection with S. aureus.
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Public Web Portal
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Internal Contract Collaboration Site