Title
Pvmsp8 as a novel plasmodium vivax malaria sero-marker for the peruvian amazon
Date Issued
01 March 2021
Access level
open access
Resource Type
journal article
Author(s)
Garro K.
Rodriguez P.
Rosado J.
Gave A.
White M.
Speybroeck N.
Publisher(s)
MDPI AG
Abstract
The measurement of recent malaria exposure can support malaria control efforts. This study evaluated serological responses to an in-house Plasmodium vivax Merozoite Surface Protein 8 (PvMSP8) expressed in a Baculovirus system as sero-marker of recent exposure to P. vivax (Pv) in the Peruvian Amazon. In a first evaluation, IgGs against PvMSP8 and PvMSP10 proteins were measured by Luminex in a cohort of 422 Amazonian individuals with known history of Pv exposure (monthly data of infection status by qPCR and/or microscopy over five months). Both serological responses were able to discriminate between exposed and non-exposed individuals in a good manner, with slightly higher performance of anti-PvMSP10 IgGs (area under the curve AUC = 0.78 [95% CI = 0.72–0.83]) than anti-PvMSP8 IgGs (AUC = 0.72 [95% CI = 0.67–0.78]) (p = 0.01). In a second evaluation, the analysis by ELISA of 1251 plasma samples, collected during a population-based cross-sectional survey, confirmed the good performance of anti-PvMSP8 IgGs for discriminating between individuals with Pv infection at the time of survey and/or with antecedent of Pv in the past month (AUC = 0.79 [95% CI = 0.74–0.83]). Anti-PvMSP8 IgG antibodies can be considered as a good biomarker of recent Pv exposure in low-moderate transmission settings of the Peruvian Amazon.
Start page
1
End page
23
Volume
10
Issue
3
Language
English
OCDE Knowledge area
Patología
Subjects
Scopus EID
2-s2.0-85102554474
Source
Pathogens
ISSN of the container
20760817
Source funding
Source project
Sponsor(s)
Acknowledgments: We thank all residents and local authorities from the Loreto Communities of Cahuide, Lupuna, and Mazan District for their enthusiastic participation in the study, as well as all field workers for their dedication during the fieldwork. E. Villasis acknowledges the financial support of the Project CONCYTEC-World Bank “Improvement and Expansion of Services of the National System of Science, Technology and Technological Innovation ” 8682-PE, through its executing unit FONDECYT [contract number 08-2018-E033-FONDECYT-BM-Programas de Doctorado en Áreas Estratégicas y Generales] for her research work. P.R. and A.R.-A. acknowledge the financial support of the Project CONCYTEC–ERANet-LAC “Serosurveillance tools for targeting Plasmodium vivax infections and monitoring malaria control and elimination efforts in Amazonian countries” [contract number 111-2016-FONDECYT]. We also thank the logistic and administrative support of Beronica Infante, Yulissa Vasquez, Yovana Maldonado, and Joaquin Gomez from the Malaria Laboratory at UPCH. Finally, we thank Amy Bei of the Yale School of Public Health and her team and human volunteers in Senegal for the use of blood samples in this study.
Funding: This research was funded by: “Fondo Nacional de Desarrollo Científico, Tecnológico y de Innovación Tecnológica” (FONDECYT/CONCYTEC), under the Contract 218-2015-FONDECYT; The International Centers of Excellence for Malaria Research (ICEMR) program (U19AI089681), NIH–USA; FOGARTY International Center (D43TW007120), NIH-USA. EV is supported by the CONCYTEC-FONDECYT-World Bank Group contract number E033-01-08-2018-FONDECYT/Banco Mundial-Programas de Doctorado en Áreas Estratégicas y Generales. ARA is a Postdoctoral Researcher of the Fonds de la Recherche Scientifique (FNRS, Belgium).
Sources of information:
Directorio de Producción Científica
Scopus