Sterile protection againstP. vivaxmalaria by repeated blood stage infection in theAotusmonkey model

Author:

Obaldía Nicanor123ORCID,Da Silva Filho Joao Luiz34,Núñez Marlon1,Glass Katherine A5,Oulton Tate5,Achcar Fiona34,Wirjanata Grennady6,Duraisingh Manoj2,Felgner Philip7,Tetteh Kevin KA5,Bozdech Zbynek6,Otto Thomas D3ORCID,Marti Matthias234ORCID

Affiliation:

1. Departamento de Investigaciones en Parasitologia, Instituto Conmemorativo Gorgas de Estudios de la Salud, Panamá City, Republic of Panamá

2. Department of Immunology and Infectious Diseases, Harvard TH Chan School of Public Health, Harvard University, Boston, MA, USA

3. Wellcome Centre for Integrative Parasitology, School of Infection and Immunity, College of Medical, Veterinary and Life Sciences, University of Glasgow

4. Institute of Parasitology, Vetsuisse and Medical Faculty, University of Zurich

5. Department of Immunology and Infection, London School of Hygiene and Tropical Medicine, London, UK

6. School of Biological Sciences, Nanyang Technological University, Singapore, Singapore

7. Institute for Immunology, University of California, Irvine, CA, USA

Abstract

The malaria parasitePlasmodium vivaxremains a major global public health challenge, and no vaccine is approved for use in humans. Here, we assessed whetherP. vivaxstrain-transcendent immunity can be achieved by repeated infection inAotusmonkeys. Sterile immunity was achieved after two homologous infections, whereas subsequent heterologous challenge provided only partial protection. IgG levels based onP. vivaxlysate ELISA and protein microarray increased with repeated infections and correlated with the level of homologous protection. Parasite transcriptional profiles provided no evidence of major antigenic switching upon homologous or heterologous challenge. However, we observed significant sequence diversity and transcriptional differences in theP. vivaxcore gene repertoire between the two strains used in the study, suggesting that partial protection upon heterologous challenge is due to molecular differences between strains rather than immune evasion by antigenic switching. Our study demonstrates that sterile immunity againstP. vivaxcan be achieved by repeated homologous blood stage infection inAotusmonkeys, thus providing a benchmark to test the efficacy of candidate blood stageP. vivaxmalaria vaccines.

Funder

SENACYT | Sistema Nacional de Investigación, Secretaría Nacional de Ciencia, Tecnología e Innovación

Royal Society Wolfson Research Merit Award

Wellcome Trust

Publisher

Life Science Alliance, LLC

Subject

Health, Toxicology and Mutagenesis,Plant Science,Biochemistry, Genetics and Molecular Biology (miscellaneous),Ecology

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