Plasmodium falciparum gametocyte dynamics after pyronaridine–artesunate or artemether–lumefantrine treatment
Abstract Background Artemisinin-based combinations differ in their impact on gametocyte prevalence and density. This study assessed female and male gametocyte dynamics after treating children with uncomplicated Plasmodium falciparum malaria with either pyronaridine–artesunate (PA) or artemether–lume...
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doaj-e7b5dd92fde04f3b85817ca1b1a9e4a82020-11-25T00:12:12ZengBMCMalaria Journal1475-28752018-06-0117111110.1186/s12936-018-2373-7Plasmodium falciparum gametocyte dynamics after pyronaridine–artesunate or artemether–lumefantrine treatmentJohanna M. Roth0Patrick Sawa1George Omweri2Victor Osoti3Nicodemus Makio4John Bradley5Teun Bousema6Henk D. F. H. Schallig7Pètra F. Mens8Department of Medical Microbiology, Laboratory for Clinical Parasitology, Academic Medical CenterHuman Health Division, International Centre of Insect Physiology and EcologyHuman Health Division, International Centre of Insect Physiology and EcologyHuman Health Division, International Centre of Insect Physiology and EcologyHuman Health Division, International Centre of Insect Physiology and EcologyMedical Research Council Tropical Epidemiology Group, London School of Hygiene and Tropical MedicineRadboud Institute for Health Sciences, Radboud University Medical CenterDepartment of Medical Microbiology, Laboratory for Clinical Parasitology, Academic Medical CenterDepartment of Medical Microbiology, Laboratory for Clinical Parasitology, Academic Medical CenterAbstract Background Artemisinin-based combinations differ in their impact on gametocyte prevalence and density. This study assessed female and male gametocyte dynamics after treating children with uncomplicated Plasmodium falciparum malaria with either pyronaridine–artesunate (PA) or artemether–lumefantrine (AL). Methods Kenyan children with uncomplicated Plasmodium falciparum malaria were included and randomly assigned to PA or AL treatment. Filter paper blood samples were collected as a source of RNA for quantitative reverse-transcription PCR (qRT-PCR) and nucleic acid sequence based amplification (QT-NASBA) to detect female gametocytes (targeting Pfs25 mRNA). Male gametocytes were detected by qRT-PCR (targeting PfMGET mRNA). Duration of gametocyte carriage, the female and male gametocyte response and the agreement between qRT-PCR and QT-NASBA were determined. Results The mean duration of female gametocyte carriage was significantly longer for PA (4.9 days) than for AL (3.8 days) as estimated by QT-NASBA (P = 0.036), but this difference was less clear when determined by Pfs25 qRT-PCR (4.5 days for PA and 3.7 for AL, P = 0.166). qRT-PCR based female gametocyte prevalence decreased from 100% (75/75) at baseline to 6.06% (4/66) at day 14 in the AL group and from 97.7% (83/85) to 13.9% (11/79) in the PA group. Male gametocyte prevalence decreased from 41.3% (31/75) at baseline to 19.7% (13/66) at day 14 in the AL group and from 35.3% (30/85) to 22.8% (18/79) in the PA group. There was good agreement between Pfs25 qRT-PCR and QT-NASBA female gametocyte prevalence (0.85, 95% CI 0.82–0.87). Conclusions This study indicates that female gametocyte clearance may be slightly faster after AL compared to PA. Male gametocytes showed similar post-treatment clearance between study arms. Future studies should further address potential differences between the post-treatment transmission potential after PA compared to AL. Trial registration This study is registered at clinicaltrials.gov under NCT02411994. Registration date: 8 April 2015. https://clinicaltrials.gov/ct2/show/NCT02411994?term=pyronaridine-artesunate&cond=Malaria&cntry=KE&rank=1http://link.springer.com/article/10.1186/s12936-018-2373-7Plasmodium falciparumGametocytesArtemether–lumefantrinePyronaridine–artesunate |
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language |
English |
format |
Article |
sources |
DOAJ |
author |
Johanna M. Roth Patrick Sawa George Omweri Victor Osoti Nicodemus Makio John Bradley Teun Bousema Henk D. F. H. Schallig Pètra F. Mens |
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Johanna M. Roth Patrick Sawa George Omweri Victor Osoti Nicodemus Makio John Bradley Teun Bousema Henk D. F. H. Schallig Pètra F. Mens Plasmodium falciparum gametocyte dynamics after pyronaridine–artesunate or artemether–lumefantrine treatment Malaria Journal Plasmodium falciparum Gametocytes Artemether–lumefantrine Pyronaridine–artesunate |
author_facet |
Johanna M. Roth Patrick Sawa George Omweri Victor Osoti Nicodemus Makio John Bradley Teun Bousema Henk D. F. H. Schallig Pètra F. Mens |
author_sort |
Johanna M. Roth |
title |
Plasmodium falciparum gametocyte dynamics after pyronaridine–artesunate or artemether–lumefantrine treatment |
title_short |
Plasmodium falciparum gametocyte dynamics after pyronaridine–artesunate or artemether–lumefantrine treatment |
title_full |
Plasmodium falciparum gametocyte dynamics after pyronaridine–artesunate or artemether–lumefantrine treatment |
title_fullStr |
Plasmodium falciparum gametocyte dynamics after pyronaridine–artesunate or artemether–lumefantrine treatment |
title_full_unstemmed |
Plasmodium falciparum gametocyte dynamics after pyronaridine–artesunate or artemether–lumefantrine treatment |
title_sort |
plasmodium falciparum gametocyte dynamics after pyronaridine–artesunate or artemether–lumefantrine treatment |
publisher |
BMC |
series |
Malaria Journal |
issn |
1475-2875 |
publishDate |
2018-06-01 |
description |
Abstract Background Artemisinin-based combinations differ in their impact on gametocyte prevalence and density. This study assessed female and male gametocyte dynamics after treating children with uncomplicated Plasmodium falciparum malaria with either pyronaridine–artesunate (PA) or artemether–lumefantrine (AL). Methods Kenyan children with uncomplicated Plasmodium falciparum malaria were included and randomly assigned to PA or AL treatment. Filter paper blood samples were collected as a source of RNA for quantitative reverse-transcription PCR (qRT-PCR) and nucleic acid sequence based amplification (QT-NASBA) to detect female gametocytes (targeting Pfs25 mRNA). Male gametocytes were detected by qRT-PCR (targeting PfMGET mRNA). Duration of gametocyte carriage, the female and male gametocyte response and the agreement between qRT-PCR and QT-NASBA were determined. Results The mean duration of female gametocyte carriage was significantly longer for PA (4.9 days) than for AL (3.8 days) as estimated by QT-NASBA (P = 0.036), but this difference was less clear when determined by Pfs25 qRT-PCR (4.5 days for PA and 3.7 for AL, P = 0.166). qRT-PCR based female gametocyte prevalence decreased from 100% (75/75) at baseline to 6.06% (4/66) at day 14 in the AL group and from 97.7% (83/85) to 13.9% (11/79) in the PA group. Male gametocyte prevalence decreased from 41.3% (31/75) at baseline to 19.7% (13/66) at day 14 in the AL group and from 35.3% (30/85) to 22.8% (18/79) in the PA group. There was good agreement between Pfs25 qRT-PCR and QT-NASBA female gametocyte prevalence (0.85, 95% CI 0.82–0.87). Conclusions This study indicates that female gametocyte clearance may be slightly faster after AL compared to PA. Male gametocytes showed similar post-treatment clearance between study arms. Future studies should further address potential differences between the post-treatment transmission potential after PA compared to AL. Trial registration This study is registered at clinicaltrials.gov under NCT02411994. Registration date: 8 April 2015. https://clinicaltrials.gov/ct2/show/NCT02411994?term=pyronaridine-artesunate&cond=Malaria&cntry=KE&rank=1 |
topic |
Plasmodium falciparum Gametocytes Artemether–lumefantrine Pyronaridine–artesunate |
url |
http://link.springer.com/article/10.1186/s12936-018-2373-7 |
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