Molecular detection and quantification of Plasmodium falciparum gametocytes carriage in used RDTs in malaria elimination settings in northern Senegal

Abstract Background Malaria surveillance requires powerful tools and strategies to achieve malaria elimination. Rapid diagnostic tests for malaria (RDTs) are easily deployed on a large scale and are helpful sources of parasite DNA. The application of sensitive molecular techniques to these RDTs is a...

Full description

Bibliographic Details
Main Authors: Kiswendsida Thierry Guiguemde, Yakou Dieye, Aminata Collé Lô, Magatte Ndiaye, Aminata Lam, Isaac Akhénaton Manga, Gnagna Dieng Sow, Moussa Diop, Tamba Souané, Marie Pièrre Diouf, Roger Clément Kouly Tine, Babacar Faye
Format: Article
Language:English
Published: BMC 2020-03-01
Series:Malaria Journal
Subjects:
RDT
Online Access:http://link.springer.com/article/10.1186/s12936-020-03204-w
id doaj-4d34de6173f34c23a3c15eb19ebb8864
record_format Article
spelling doaj-4d34de6173f34c23a3c15eb19ebb88642020-11-25T02:29:21ZengBMCMalaria Journal1475-28752020-03-011911710.1186/s12936-020-03204-wMolecular detection and quantification of Plasmodium falciparum gametocytes carriage in used RDTs in malaria elimination settings in northern SenegalKiswendsida Thierry Guiguemde0Yakou Dieye1Aminata Collé Lô2Magatte Ndiaye3Aminata Lam4Isaac Akhénaton Manga5Gnagna Dieng Sow6Moussa Diop7Tamba Souané8Marie Pièrre Diouf9Roger Clément Kouly Tine10Babacar Faye11Department of Medical Parasitology, Medical Faculty, Cheikh Anta Diop UniversityPATH, Malaria Control and Evaluation Partnership (MACEPA)Department of Medical Parasitology, Medical Faculty, Cheikh Anta Diop UniversityDepartment of Medical Parasitology, Medical Faculty, Cheikh Anta Diop UniversityDepartment of Medical Parasitology, Medical Faculty, Cheikh Anta Diop UniversityDepartment of Medical Parasitology, Medical Faculty, Cheikh Anta Diop UniversityPATH, Malaria Control and Evaluation Partnership (MACEPA)PATH, Malaria Control and Evaluation Partnership (MACEPA)PATH, Malaria Control and Evaluation Partnership (MACEPA)Department of Medical Parasitology, Medical Faculty, Cheikh Anta Diop UniversityDepartment of Medical Parasitology, Medical Faculty, Cheikh Anta Diop UniversityDepartment of Medical Parasitology, Medical Faculty, Cheikh Anta Diop UniversityAbstract Background Malaria surveillance requires powerful tools and strategies to achieve malaria elimination. Rapid diagnostic tests for malaria (RDTs) are easily deployed on a large scale and are helpful sources of parasite DNA. The application of sensitive molecular techniques to these RDTs is a modern tool for improving malaria case detection and drug resistance surveillance. Several studies have made it possible to extract the DNA of Plasmodium falciparum from RDTs. The knowledge of gametocyte carriage in the population is important to better assess the level of parasite transmission in elimination settings. The aim of this study was to detect P. falciparum gametocytes from used RDTs by quantitative PCR for molecular monitoring of malaria transmission. Methods DNA was extracted from 303 RDT devices (SD Bioline Malaria Pf) using the Chelex-100 protocol. qPCR was performed in a 20 μL reaction to detect and quantify transcripts of the pfs25 gene. The cycle threshold (Ct) was determined by the emission fluorescence corresponding to the initial amount of amplified DNA. Results The study found an overall prevalence of 53.47% with an average Ct of 32.12 ± 4.28 cycles. In 2018, the prevalence of gametocytes was higher in the Ranérou district (76.24%) than in the Saint-Louis district (67.33%) where an increase in the number of gametocyte carriers in 2018 was noted, in comparison with 2017. Conclusions RDTs are a good source of DNA for molecular monitoring of gametocyte carriage. This method is a simple and effective tool to better understand the level of malaria transmission with a view to elimination.http://link.springer.com/article/10.1186/s12936-020-03204-wMalariaRDTGametocytesDNA extractionQuantificationPlasmodium falciparum
collection DOAJ
language English
format Article
sources DOAJ
author Kiswendsida Thierry Guiguemde
Yakou Dieye
Aminata Collé Lô
Magatte Ndiaye
Aminata Lam
Isaac Akhénaton Manga
Gnagna Dieng Sow
Moussa Diop
Tamba Souané
Marie Pièrre Diouf
Roger Clément Kouly Tine
Babacar Faye
spellingShingle Kiswendsida Thierry Guiguemde
Yakou Dieye
Aminata Collé Lô
Magatte Ndiaye
Aminata Lam
Isaac Akhénaton Manga
Gnagna Dieng Sow
Moussa Diop
Tamba Souané
Marie Pièrre Diouf
Roger Clément Kouly Tine
Babacar Faye
Molecular detection and quantification of Plasmodium falciparum gametocytes carriage in used RDTs in malaria elimination settings in northern Senegal
Malaria Journal
Malaria
RDT
Gametocytes
DNA extraction
Quantification
Plasmodium falciparum
author_facet Kiswendsida Thierry Guiguemde
Yakou Dieye
Aminata Collé Lô
Magatte Ndiaye
Aminata Lam
Isaac Akhénaton Manga
Gnagna Dieng Sow
Moussa Diop
Tamba Souané
Marie Pièrre Diouf
Roger Clément Kouly Tine
Babacar Faye
author_sort Kiswendsida Thierry Guiguemde
title Molecular detection and quantification of Plasmodium falciparum gametocytes carriage in used RDTs in malaria elimination settings in northern Senegal
title_short Molecular detection and quantification of Plasmodium falciparum gametocytes carriage in used RDTs in malaria elimination settings in northern Senegal
title_full Molecular detection and quantification of Plasmodium falciparum gametocytes carriage in used RDTs in malaria elimination settings in northern Senegal
title_fullStr Molecular detection and quantification of Plasmodium falciparum gametocytes carriage in used RDTs in malaria elimination settings in northern Senegal
title_full_unstemmed Molecular detection and quantification of Plasmodium falciparum gametocytes carriage in used RDTs in malaria elimination settings in northern Senegal
title_sort molecular detection and quantification of plasmodium falciparum gametocytes carriage in used rdts in malaria elimination settings in northern senegal
publisher BMC
series Malaria Journal
issn 1475-2875
publishDate 2020-03-01
description Abstract Background Malaria surveillance requires powerful tools and strategies to achieve malaria elimination. Rapid diagnostic tests for malaria (RDTs) are easily deployed on a large scale and are helpful sources of parasite DNA. The application of sensitive molecular techniques to these RDTs is a modern tool for improving malaria case detection and drug resistance surveillance. Several studies have made it possible to extract the DNA of Plasmodium falciparum from RDTs. The knowledge of gametocyte carriage in the population is important to better assess the level of parasite transmission in elimination settings. The aim of this study was to detect P. falciparum gametocytes from used RDTs by quantitative PCR for molecular monitoring of malaria transmission. Methods DNA was extracted from 303 RDT devices (SD Bioline Malaria Pf) using the Chelex-100 protocol. qPCR was performed in a 20 μL reaction to detect and quantify transcripts of the pfs25 gene. The cycle threshold (Ct) was determined by the emission fluorescence corresponding to the initial amount of amplified DNA. Results The study found an overall prevalence of 53.47% with an average Ct of 32.12 ± 4.28 cycles. In 2018, the prevalence of gametocytes was higher in the Ranérou district (76.24%) than in the Saint-Louis district (67.33%) where an increase in the number of gametocyte carriers in 2018 was noted, in comparison with 2017. Conclusions RDTs are a good source of DNA for molecular monitoring of gametocyte carriage. This method is a simple and effective tool to better understand the level of malaria transmission with a view to elimination.
topic Malaria
RDT
Gametocytes
DNA extraction
Quantification
Plasmodium falciparum
url http://link.springer.com/article/10.1186/s12936-020-03204-w
work_keys_str_mv AT kiswendsidathierryguiguemde moleculardetectionandquantificationofplasmodiumfalciparumgametocytescarriageinusedrdtsinmalariaeliminationsettingsinnorthernsenegal
AT yakoudieye moleculardetectionandquantificationofplasmodiumfalciparumgametocytescarriageinusedrdtsinmalariaeliminationsettingsinnorthernsenegal
AT aminatacollelo moleculardetectionandquantificationofplasmodiumfalciparumgametocytescarriageinusedrdtsinmalariaeliminationsettingsinnorthernsenegal
AT magattendiaye moleculardetectionandquantificationofplasmodiumfalciparumgametocytescarriageinusedrdtsinmalariaeliminationsettingsinnorthernsenegal
AT aminatalam moleculardetectionandquantificationofplasmodiumfalciparumgametocytescarriageinusedrdtsinmalariaeliminationsettingsinnorthernsenegal
AT isaacakhenatonmanga moleculardetectionandquantificationofplasmodiumfalciparumgametocytescarriageinusedrdtsinmalariaeliminationsettingsinnorthernsenegal
AT gnagnadiengsow moleculardetectionandquantificationofplasmodiumfalciparumgametocytescarriageinusedrdtsinmalariaeliminationsettingsinnorthernsenegal
AT moussadiop moleculardetectionandquantificationofplasmodiumfalciparumgametocytescarriageinusedrdtsinmalariaeliminationsettingsinnorthernsenegal
AT tambasouane moleculardetectionandquantificationofplasmodiumfalciparumgametocytescarriageinusedrdtsinmalariaeliminationsettingsinnorthernsenegal
AT mariepierrediouf moleculardetectionandquantificationofplasmodiumfalciparumgametocytescarriageinusedrdtsinmalariaeliminationsettingsinnorthernsenegal
AT rogerclementkoulytine moleculardetectionandquantificationofplasmodiumfalciparumgametocytescarriageinusedrdtsinmalariaeliminationsettingsinnorthernsenegal
AT babacarfaye moleculardetectionandquantificationofplasmodiumfalciparumgametocytescarriageinusedrdtsinmalariaeliminationsettingsinnorthernsenegal
_version_ 1724833652825653248