Journal article

Utility of ultra-sensitive qPCR to detect Plasmodium falciparum and Plasmodium vivax infections under different transmission intensities

M Gruenberg, CA Moniz, NE Hofmann, C Koepfli, LJ Robinson, E Nate, WM Monteiro, GC De Melo, A Kuehn, AM Siqueira, W Nguitragool, Q Bassat, M Lacerda, J Sattabongkot, I Mueller, I Felger

Malaria Journal | BMC | Published : 2020

Abstract

Background: The use of molecular diagnostics has revealed an unexpectedly large number of asymptomatic low-density malaria infections in many malaria endemic areas. This study compared the gains in parasite prevalence obtained by the use of ultra-sensitive (us)-qPCR as compared to standard qPCR in cross-sectional surveys conducted in Thailand, Brazil and Papua New Guinea (PNG). The compared assays differed in the copy number of qPCR targets in the parasite genome. Methods: Plasmodium falciparum (Pf) and Plasmodium vivax (Pv) parasites were quantified by qPCR amplifying the low-copy Pf_ and Pv_18S rRNA genes or the multi-copy targets Pf_varATS and Pv_mtCOX1. Cross-sectional surveys at the thr..

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University of Melbourne Researchers

Grants

Awarded by Swiss National Science Foundation


Awarded by TransEPi Consortium/Bill and Melinda Gates Foundation


Awarded by NIH


Awarded by Swiss National Science Foundation (SNF)


Awarded by Bill and Melinda Gates Foundation


Funding Acknowledgements

This study was funded by the Swiss National Science Foundation (grants no. 310030_159580 and IZRJZ3_164182), the TransEPi Consortium/Bill and Melinda Gates Foundation (OPP1034577) and by the NIH (1 U19 AI089686-01). IM was supported by an NHMRC Senior Research Fellowship.