Proteomic Analysis ofPichindé virusInfection Identifies Differential Expression of Prothymosin-α

Author:

Bowick Gavin C.123,Soman Kizhake V.4,Wang He5,Aronson Judith F.346,Luxon Bruce A.346,Lomas Lee O.5,Gorenstein David G.347,Herzog Norbert K.123

Affiliation:

1. Department of Pathology, University of Texas Medical Branch, Galveston, TX 77555-0609, USA

2. Department of Microbiology & Immunology, University of Texas Medical Branch, Galveston, TX 77555-0609, USA

3. Center for Biodefense and Emerging Infectious Diseases, University of Texas Medical Branch, Galveston, TX 77555-0609, USA

4. Department of Biochemistry & Molecular Biology, University of Texas Medical Branch, Galveston, TX 77555-0609, USA

5. Bio-Rad Laboratories, 6000 James Watson Drive, Hercules, CA 94547, USA

6. Bioinformatics Program, University of Texas Medical Branch, Galveston, TX 77555-0609, USA

7. Centers for Proteomics and Systems Biology, Brown Institute for Molecular Medicine, University of Texas Health Science Center, Houston, TX 77030, USA

Abstract

The arenaviruses include a number of important pathogens includingLassa virusandJunin virus. Presently, the only treatment is supportive care and the antiviral Ribavirin. In the event of an epidemic, patient triage may be required to more effectively manage resources; the development of prognostic biomarker signatures, correlating with disease severity, would allow rational triage. Using a pair of arenaviruses, which cause mild or severe disease, we analyzed extracts from infected cells using SELDI mass spectrometry to characterize potential biomarker profiles. EDGE analysis was used to analyze longitudinal expression differences. Extracts from infected guinea pigs revealed protein peaks which could discriminate between mild or severe infection and between times post-infection. Tandem mass-spectrometry identified several peaks, including the transcriptional regulator prothymosin-α. Further investigation revealed differences in secretion of this peptide. These data show proof of concept that proteomic profiling of host markers could be used as prognostic markers of infectious disease.

Funder

National Institutes of Health

Publisher

Hindawi Limited

Subject

Health, Toxicology and Mutagenesis,Genetics,Molecular Biology,Molecular Medicine,General Medicine,Biotechnology

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