2022 |
|
Journal Articles |
|
Charlie Franck Alfred Compaoré, Jacques Kaboré, Hamidou Ilboudo, Lian Francesca Thomas, Laura Cristina Falzon, Mohamed Bamba, Hassane Sakande, Minayégninrin Koné, Dramane Kaba, Clarisse Bougouma, Ilboudo Adama, Ouedraogo Amathe, Adrien Marie Gaston Belem, Eric Maurice Fèvre, Philippe Büscher, Veerle Lejon, Vincent Jamonneau In: Parasite, vol. 29, pp. 25, 2022, ISSN: 1776-1042. (Abstract | Links | BibTeX | Tags: Burkina Faso, Diagnosis, Dried blood spot, Elimination, Human African trypanosomiasis, Rapid diagnostic test, Specificity, Trypanosoma brucei gambiense) @article{nokey, <p> The World Health Organisation has targeted the elimination of human African trypanosomiasis (HAT) as zero transmission by 2030. Continued surveillance needs to be in place for early detection of re-emergent cases. In this context, the performance of diagnostic tests and testing algorithms for detection of the re-emergence of <italic>Trypanosoma brucei gambiense</italic> HAT remains to be assessed. We carried out a door-to-door active medical survey for HAT in the historical focus of Batié, South–West Burkina Faso. Screening was done using three rapid diagnostic tests (RDTs). Two laboratory tests (ELISA/ <italic>T. b. gambiense</italic> and immune trypanolysis) and parasitological examination were performed on RDT positives only. In total, 5883 participants were screened, among which 842 (14%) tested positive in at least one RDT. Blood from 519 RDT positives was examined microscopically but no trypanosomes were observed. The HAT Sero- <italic>K</italic> -Set test showed the lowest specificity of 89%, while the specificities of SD Bioline HAT and rHAT Sero-Strip were 92% and 99%, respectively. The specificity of ELISA/ <italic>T. b. gambiense</italic> and trypanolysis was 99% (98–99%) and 100% (99–100%), respectively. Our results suggest that <italic>T. b. gambiense</italic> is no longer circulating in the study area and that zero transmission has probably been attained. While a least cost analysis is still required, our study showed that RDT preselection followed by trypanolysis may be a useful strategy for post-elimination surveillance in Burkina Faso. </p> | |
2020 |
|
Journal Articles |
|
Charlie Franck Alfred Compaoré, Hamidou Ilboudo, Jacques Kaboré, Justin Windingoudi Kaboré, Oumou Camara, Mohamed Bamba, Hassane Sakande, Minayégninrin Koné, Mamadou Camara, Dramane Kaba, Adrien Marie Gaston Belem, Stijn Deborggraeve, Philippe Büscher, Bruno Bucheton, Veerle Lejon, Vincent Jamonneau In: Experimental parasitology, vol. 219, pp. 108014, 2020, ISSN: 1090-2449 0014-4894. (Abstract | Links | BibTeX | Tags: African/blood/diagnosis/*prevention & control, Algorithms, Animals, Blood Specimen Collection/methods/standards, Diagnosis, DNA, Dried blood spots, Feasibility, High-Throughput Screening Assays/methods/standards, Humans, Loopamp, Mice, Molecular Diagnostic Techniques/*standards, Nucleic Acid Amplification Techniques/*standards, Protozoan/isolation & purification, Quantitative real-time PCR, Real-Time Polymerase Chain Reaction/methods/*standards, Sensitivity, Sensitivity and Specificity, Specimen Handling/methods/standards, Trypanosoma brucei gambiense, Trypanosoma brucei gambiense/genetics/*isolation & purification, Trypanosomiasis) @article{nokey, The objective set by WHO to reach elimination of human African trypanosomiasis (HAT) as a public health problem by 2020 is being achieved. The next target is the interruption of gambiense-HAT transmission in humans by 2030. To monitor progress towards this target, in areas where specialized local HAT control capacities will disappear, is a major challenge. Test specimens should be easily collectable and safely transportable such as dried blood spots (DBS). Monitoring tests performed in regional reference centres should be reliable, cheap and allow analysis of large numbers of specimens in a high-throughput format. The aim of this study was to assess the analytical sensitivity of Loopamp, M18S quantitative real-time PCR (M18S qPCR) and TgsGP qPCR as molecular diagnostic tests for the presence of Trypanosoma brucei gambiense in DBS. The sensitivity of the Loopamp test, with a detection limit of 100 trypanosomes/mL, was in the range of parasitaemias commonly observed in HAT patients, while detection limits for M18S and TgsGP qPCR were respectively 1000 and 10,000 trypanosomes/mL. None of the tests was entirely suitable for high-throughput use and further development and implementation of sensitive high-throughput molecular tools for monitoring HAT elimination are needed. |
Input your search keywords and press Enter.