Plasma Proteomic Analysis Distinguishes Severity Outcomes of Human Ebola Virus Disease

Author:

Viodé Arthur12,Smolen Kinga K.234,Fatou Benoit123,Wurie Zainab1,Van Zalm Patrick12,Konde Mandy Kader56,Keita Balla Moussa56,Ablam Richard Amento5,Fish Eleanor N.78,Steen Hanno123

Affiliation:

1. Department of Pathology, Boston Children’s Hospital, Boston, Massachusetts, USA

2. Harvard Medical School, Boston, Massachusetts, USA

3. Precision Vaccines Program, Boston Children’s Hospital, Boston, Massachusetts, USA

4. Division of Infectious Diseases, Boston Children’s Hospital, Boston, Massachusetts, USA

5. Sustainable Health Foundation (FOSAD), Conakry, Guinea

6. Center of Excellence for Training on Research and Priority Diseases (CEFORPAG), Conakry, Guinea

7. Toronto General Hospital Research Institute, University Health Network, Toronto, Canada

8. Department of Immunology, University of Toronto, Toronto, Canada

Abstract

As evidenced by the 2013–2016 outbreak in West Africa, Ebola virus (EBV) disease (EVD) poses a major global health threat. In this study, we characterized the plasma proteomes of 12 individuals infected with EBV, using two different LC-MS-based proteomics platforms and an antibody-based multiplexed cytokine/chemokine assay.

Funder

Gouvernement du Canada | Canadian Institutes of Health Research

Publisher

American Society for Microbiology

Subject

Virology,Microbiology

Reference74 articles.

1. World Health Organization. 2017. Ebola outbreak 2014-2016. World Health Organization, Geneva, Switzerland. http://www.who.int/csr/disease/ebola/en/.

2. Ebola virus disease

3. Ebola and Marburg Hemorrhagic Fever

4. The Ebola virus VP35 protein functions as a type I IFN antagonist

5. The ebolavirus VP24 interferon antagonist

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