Adaptation to a Multiplex Bead Assay and Seroprevalence to Rift Valley Fever N Protein: Nampula Province, Mozambique, 2013-2014

Author:

Rogier Eric1ORCID,Plucinski Mateusz12ORCID,Candrinho Baltazar3,Moss Delynn M.4,Gibbons Aridth5,Colborn James6,Higgins Jeffrey7,Chambe Geraldo8,Muchanga Joao8,Muguande Olinda3,Matsinhe Graca3,Mathe Guidion3,Doyle Timothy9,Zulliger Rose12,Saifodine Abu10,Montgomery Joel M.5,Klena John D.5,Priest Jeffrey W.4

Affiliation:

1. Division of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, Georgia, USA

2. US President's Malaria Initiative, Centers for Disease Control and Prevention, Atlanta, Georgia, USA

3. National Malaria Control Program, Ministry of Health, Maputo, Mozambique, Africa

4. Division of Foodborne, Waterborne, and Environmental Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA

5. Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia, USA

6. Clinton Health Access Initiative, Boston, Massachusetts, USA

7. Office of Innovation and Analytics, Centers for Disease Control and Prevention/Agency for Toxic Substances and Disease Registry, Atlanta, Georgia, USA

8. Mozambique Field Epidemiology and Laboratory Training Program, Maputo, Mozambique, Africa

9. Field Epidemiology and Laboratory Training Program, Centers for Disease Control and Prevention, Maputo, Mozambique, Africa

10. US President's Malaria Initiative, United States Agency for International Development, Maputo, Mozambique, Africa

Abstract

Due to sporadic transmission, human contact with Rift Valley Fever Virus (RVFV) is difficult to ascertain at a population level. Detection of antibodies against RVFV antigens assist in estimating exposure as antibodies remain in the host long after the virus has been cleared.

Funder

United States Agency for International Development

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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