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Plasmodium falciparum Gametocyte Enrichment in Peripheral Blood Samples by Magnetic Fractionation: Gametocyte Yields and Possibilities to Reuse Columns.
Graumans, Wouter; Andolina, Chiara; Awandu, Shehu S; Grignard, Lynn; Lanke, Kjerstin; Bousema, Teun.
Affiliation
  • Graumans W; Department of Medical Microbiology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
  • Andolina C; Department of Medical Microbiology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
  • Awandu SS; Department of Medical Microbiology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
  • Grignard L; Department of Immunology and Infection, London School of Hygiene and Tropical Medicine, London, United Kingdom.
  • Lanke K; Department of Medical Microbiology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
  • Bousema T; Department of Medical Microbiology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
Am J Trop Med Hyg ; 100(3): 572-577, 2019 03.
Article in En | MEDLINE | ID: mdl-30608048
Gametocytes are sexual stage malaria parasites responsible for transmission to mosquitoes. Multiple gametocyte-producing clones may be present in natural infections, but the molecular characterization of gametocytes is challenging. Because of their magnetic properties, gametocyte enrichment can be achieved by magnetic fractionation. This increases detection sensitivity and allows specific genotyping of clones that contribute to malaria transmission. Here, we determined the percentage of Plasmodium falciparum gametocytes successfully bound to magnetic activated cell sorting (MACS) LS columns during magnetic fractionation and assessed whether columns can be reused without risking contamination or affecting column binding efficiency. Bound column fractions were quantified using multiplex quantitative reverse transcription polymerase chain reaction (qRT-PCR) for male (pfMGET) and female (CCp4) gametocytes and ring-stage asexual parasites (SBP1). To investigate cross contamination between columns, parasite strain identity was determined by merozoite surface protein 2 genotyping followed by capillary electrophoresis fragment sizing. A reproducible high percentage of gametocytes was bound to MACS LS columns with < 5% gametocytes appearing in the flow-through and < 0.6% asexual ring-stage parasites appearing in the gametocyte fraction. A high yield (> 94%) of gametocyte enrichment was achieved when columns were used up to five times with lower binding success after eight times (79%). We observed no evidence for cross contamination between columns.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Plasmodium falciparum / Cell Separation / Magnetics Limits: Humans Language: En Journal: Am J Trop Med Hyg Year: 2019 Document type: Article Affiliation country: Netherlands Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Plasmodium falciparum / Cell Separation / Magnetics Limits: Humans Language: En Journal: Am J Trop Med Hyg Year: 2019 Document type: Article Affiliation country: Netherlands Country of publication: United States