Quantitative determination of Plasmodium vivax gametocytes by real-time quantitative nucleic acid sequence-based amplification in clinical samples

Am J Trop Med Hyg. 2009 Aug;81(2):366-9.

Abstract

Microscopic detection of Plasmodium vivax gametocytes, the sexual life stage of this malaria parasite, is insensitive because P. vivax parasitaemia is low. To detect and quantify gametocytes a more sensitive, quantitative real-time Pvs25-QT-NASBA based on Pvs25 mRNA was developed and tested in two clinical sample sets from three different continents. Pvs25-QT-NASBA is highly reproducible with low inter-assay variation and reaches sensitivity approximately 800 times higher than conventional microscopic gametocyte detection. Specificity was tested in 104 samples from P. vivax-, P. falciparum-, P. malariae-, and P. ovale-infected patients. All non-vivax samples were negative in the Pvs25-QT-NASBA; out of 74 PvS18-QT-NASBA positive samples 69% were positive in the Pvs25-QT-NASBA. In a second set of 136 P. vivax microscopically confirmed samples, gametocyte prevalence was 8%, whereas in contrast 66% were positive by Pvs25-QT-NASBA. The data suggest that the human P. vivax gametocyte reservoir is much larger when assessed by Pvs25-QT-NASBA than by microscopy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Humans
  • Malaria, Vivax / parasitology*
  • Nucleic Acid Amplification Techniques / methods*
  • Plasmodium vivax / cytology
  • Plasmodium vivax / genetics
  • Plasmodium vivax / isolation & purification*
  • Protozoan Proteins / genetics
  • RNA / genetics
  • RNA, Protozoan / genetics
  • Reproducibility of Results
  • Sensitivity and Specificity

Substances

  • Protozoan Proteins
  • RNA, Protozoan
  • RNA