Zhen f fu department of pathology university of georgia
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Pathogenic and attenuated rabies viruses induces differential host protein expression in the central nervous system: Implication of neuronal dysfunction. Zhen F. Fu Department of Pathology University of Georgia. Rabies Pathogenesis. Robert Hurt-USC.

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Zhen F. Fu Department of Pathology University of Georgia

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Zhen f fu department of pathology university of georgia

Pathogenic and attenuated rabies viruses induces differential host protein expression in the central nervous system: Implication of neuronal dysfunction

Zhen F. Fu

Department of Pathology

University of Georgia


Zhen f fu department of pathology university of georgia

Rabies Pathogenesis

Robert Hurt-USC

Patients die of circulatory insufficiency,

cardiac arrest and respiratory failure.


Zhen f fu department of pathology university of georgia

Despite extensive research in the past 100 years, we still know very little about the pathogenic mechanism by which rabies virus infection of neurons causes rabies.There are scarce neuropathology with mild inflammation and little neuronal loss, which cannot explain the lethality of the disease.It has been hypothesized that rabies results from neuronal dysfunction rather than structural damage. However, it is not known how RV infection leads to neuronal dysfunction.To better understand rabies pathogenesis, we initiate a project to determine how the host responds to rabies virus infections using one street and one fixed virus. This is accomplished by using proteomics technologies.


Zhen f fu department of pathology university of georgia

Two viruses were used in this study:SHBRV: Wt virus, normally circulating in silver-haired bats and responsible for most of the human rabies in the US.CVS-B2C: Lab-adapted attenuated virus derived from CVS-24 by passaging in BHK cells.


Survival curve

Survival curve


Zhen f fu department of pathology university of georgia

Detection of Differential Protein Levels in the Proteome


Zhen f fu department of pathology university of georgia

Outline of 2-D Proteomics Strategy

MW

pH

pH

mutant/Infected

Wild type

In-gel digestion with protease

Identify the protein by Mass Spectrometry


Zhen f fu department of pathology university of georgia

2. select specific peptide

3. detect fragments

ESI

Ar

Ar

µLC

fragment peptide

Ar

1200

1000

200

400

600

800

Ar

m/z

tandem mass spectrum

1. MS “survey” scan

peptides

trypsin

4. automated database searching

gel

peptide identification

1200

1200

1000

1000

200

400

600

800

200

400

600

800

theoretical

observed

m/z

m/z

protein identification

Identification of gel-separated proteins by mass spectrometry

Gygi et al.


Zhen f fu department of pathology university of georgia

The situation to avoid…

Software is essential !


Zhen f fu department of pathology university of georgia

Proteins differentially expressed in response to SHBRV infection


Zhen f fu department of pathology university of georgia

Proteins differentially expressed in response to B2C infection in mice


Zhen f fu department of pathology university of georgia

Western blotting of proteins involved in ion homeostasis and synaptic physiology


Zhen f fu department of pathology university of georgia

Accumulation of vesicles

No Docking

No release of Neurotransmitters


Zhen f fu department of pathology university of georgia

SHBRV B2C Control


Conclusions

Conclusions

Proteomics data indicate that wt RV infection resulted in up-regulation of proteins involved in ion homeostasis and down-regulation of synaptic proteins.

The altered protein expression as detected by 2D-gel analysis is confirmed by Western blotting in animals infected either ic or im as well as in primary neuron.

Up-regulation of Na/K-ATPase leads to decrease in Na+ concentrations in infected cells. Likewise, down-regulation of Ca-ATPase resulted in decrease of Ca++ concentration in infected cells.

Changes in Na/Ca concentration affects membrane potential and thus leading to alteration of neuronal transmission.

Synaptic proteins such as syntaxin, a-SANP, and TRIM9 play important rolesin synaptic-vesicle fusion and docking of synaptic vesicles. Down-regulation of these proteins prevented the docking and fusion of synaptic vesicles with presynaptic membrane, thus resulting in accumulation of synaptic vesicles in the presynapses.

Thus our data may provide structural and metabolic basis by which RV infection causes neuronal dysfunction.


Zhen f fu department of pathology university of georgia

Acknowledgements

Vikas Dhingra

Xia-qing Li

Luciana Sarmento

UGA Proteomics Facility

Tracy Andachtc


Zhen f fu department of pathology university of georgia

Thank you!!


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