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ABSTRACT
In the era of (pre) elimination setting, the prevalence of malaria has been decreasing in most of the previously endemic areas. Therefore, effective cost- and time-saving validated pooling strategy is needed for detection of malaria in low transmission settings. In this study, optimal pooling numbers and lowest detection limit were assessed using known density samples prepared systematically, followed by genomic DNA extraction and nested PCR. Pooling strategy that composed of 10 samples in 1 pool, 20 µl in 1 sample, was optimal, and the parasite density as low as 2 p/µl for both falciparum and vivax infection was enough for detection of malaria. This pooling method showed effectiveness for handling of a huge number of samples in low transmission settings (<9% positive rate). The results indicated that pooling of the blood samples before DNA extraction followed by usual nested PCR is useful and effective for detection of malaria in screening of hidden cases in low-transmission settings.
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Mots clés
Texte intégral: 1 Indice: WPRIM Sujet Principal: Parasites / Plasmodium falciparum / Plasmodium vivax / ADN / Dépistage de masse / Réaction de polymérisation en chaîne / Prévalence / Limite de détection / Paludisme / Méthodes Type d'étude: Diagnostic_studies / Prevalence_studies / Screening_studies langue: En Texte intégral: The Korean Journal of Parasitology Année: 2016 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Parasites / Plasmodium falciparum / Plasmodium vivax / ADN / Dépistage de masse / Réaction de polymérisation en chaîne / Prévalence / Limite de détection / Paludisme / Méthodes Type d'étude: Diagnostic_studies / Prevalence_studies / Screening_studies langue: En Texte intégral: The Korean Journal of Parasitology Année: 2016 Type: Article