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Assessment of a synthetic DNA probe for Plasmodium falciparum in African blood specimens.

Authors
  • McLaughlin, G L
  • Breman, J G
  • Collins, F H
  • Schwartz, I K
  • Brandling-Bennett, A D
  • Sulzer, A J
  • Collins, W E
  • Skinner, J C
  • Ruth, J L
  • Andrysiak, P M
Type
Published Article
Journal
The American journal of tropical medicine and hygiene
Publication Date
Jul 01, 1987
Volume
37
Issue
1
Pages
27–36
Identifiers
PMID: 3300392
Source
Medline
License
Unknown

Abstract

Synthetic DNA oligomers homologous to 21-base long repetitive sequences of Plasmodium falciparum DNA were labeled with 32P using T4 kinase, and were hybridized with purified DNA and with processed blood samples from Africa. The sequence PFR1, its antiparallel oligomer PFR1R, and PFR1 covalently attached to biotin hybridized similarly to P. falciparum DNA. One-microliter aliquots of blood from Zaire spotted on prewet nylon filters and hybridized with PFR1 gave detectable autoradiogram signals from samples with parasitemias as low as 1,000 parasites/mm3. Blood lysis and protein digestion followed by alkylation allowed dot-blot processing of larger aliquots of blood. After hybridization with PFR 1 and autoradiography, 26 samples were scored positive visually, compared with 34 scored positive by microscopy. The effective sensitivity for processed 10-microliter samples was about 500 parasites/mm3. Signals from hybridized probes were quantitated by liquid scintillation counting and densitometry, and were proportional to the amounts of purified P. falciparum DNA applied to the filter. Autoradiogram signals also were roughly proportional (correlation coefficient, r = 0.77) to the number of parasites/mm3 of blood from field samples as determined by microscopic examination.

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