Detection of Plasmodium falciparum in Saliva and Stool Samples from Children Living in Franceville, a Highly Endemic Region of Gabon

Author:

Imboumy-Limoukou Roméo Karl1ORCID,Biteghe-Bi-Essone Jean-Claude1ORCID,Lendongo Wombo Judicael Boris12,Lekana-Douki Sonia Etenna3,Rougeron Virginie4,Ontoua Steede-Seinnat15ORCID,Oyegue-Liabagui Lydie Sandrine15,Mbani Mpega Ntigui Cherone Nancy15,Kouna Lady Charlène1,Lekana-Douki Jean-Bernard16ORCID

Affiliation:

1. Unité Evolution Epidémiologie et Résistance Parasitaire (UNEEREP), Centre International de Recherches Médicales de Franceville (CIRMF), Franceville BP 769, Gabon

2. Laboratoire de Biologie Moléculaire et Cellulaire (LABMC), Université des Sciences et Techniques de Masuku, Franceville BP 943, Gabon

3. Unité des Maladies Virales Emergentes (UMVE), Centre International de Recherches Médicales de Franceville, Franceville BP 769, Gabon

4. MIVEGEC, IRD, CNRS, University of Montpellier, 34900 Montpellier, France

5. Ecole Doctoral Régional en Infectiologie Tropical, Franceville BP 876, Gabon

6. Département de Parasitologie-Mycologie, Université des Sciences de la Santé, Libreville BP 4008, Gabon

Abstract

Due to the difficulty of obtaining blood samples, which is the invasive method that is currently used for the detection of Plasmodium spp., alternative diagnostic sampling methods that are effective and non-invasive are needed, particularly for long-term studies. Saliva and stool samples from malaria-infected individuals contain trace amounts of Plasmodium DNA and therefore could be used as alternatives. Malaria was screened using rapid diagnosis tests and confirmed via microscopy. Nested PCR tests targeting the Plasmodium falciparum-specific STEVOR gene were performed for blood, saliva and stool samples that were positive for malaria. Three hundred sixty-seven (367) children were enrolled and eighty (22.22%) were confirmed to be positive for malaria. Matched blood, saliva and stool samples were available for 35 children. By using blood smears as the gold standard for the diagnosis of malaria, our study indicates that Plasmodium DNA was more detectable in blood (100%) than in saliva (22.86%) and stools (14.29%). Applying qPCR to the STEVOR gene to detect Plasmodium falciparum DNA in saliva and stool samples cannot be considered as an alternative to the current malaria detection processes using blood specimens.

Publisher

MDPI AG

Subject

Clinical Biochemistry

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