Semi-high-throughput detection of Plasmodium falciparum and Plasmodium vivax oocysts in mosquitoes using bead-beating followed by circumsporozoite ELISA and quantitative PCR

Malar J. 2017 Sep 6;16(1):356. doi: 10.1186/s12936-017-2011-9.

Abstract

Background: The malaria infection status of mosquitoes is commonly determined by microscopic detection of oocysts on the dissected mosquito midgut. This method is labour-intensive, does not allow processing of large numbers of mosquitoes and can be challenging in terms of objective classification of oocysts. Here, a semi-high-throughput bead-beating ELISA method is proposed for detection of the circumsporozoite protein (CSP) followed by confirmation by quantitative PCR (qPCR).

Methods: Cultured Plasmodium falciparum gametocytes were offered to Anopheles stephensi mosquitoes and examined by microscopy. After bead-beating, mosquito homogenate was examined by CSP-ELISA and 18S qPCR. As negative controls, mosquitoes that were offered a heat-inactivated gametocyte blood meal were used. The CSP-ELISA/qPCR methodology was applied to high and low-intensity infections of cultured P. falciparum gametocytes. A similar methodology optimized for P. vivax was used on mosquitoes that were offered blood from Ethiopian donors who were naturally infected with P. vivax.

Results: There was considerable variation in CSP-ELISA signal and qPCR values in mosquitoes with low oocyst intensities. There was a strong agreement mosquito positivity by CSP-ELISA and by qPCR in mosquitoes that fed on cultured P. falciparum material (agreement 96.9%; kappa = 0.97) and naturally infected P. vivax parasite carriers [agreement 92.4% (kappa = 0.83)].

Conclusions: The proposed bead-beating CSP-ELISA/qPCR methodology considerably increases throughput for the detection of mosquito infection. qPCR remains necessary to confirm infections in mosquitoes with low CSP-ELISA signal. This methodology may prove particularly useful for studies where very low mosquito infection prevalence is expected and study sites where experience with oocyst detection is limited.

Keywords: Anopheles; Gametocyte; Infectivity; Oocyst; Sporozoite; Transmission.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anopheles / parasitology*
  • Antigens, Protozoan / blood
  • Antigens, Protozoan / isolation & purification
  • DNA, Protozoan
  • Enzyme-Linked Immunosorbent Assay / methods*
  • Female
  • Humans
  • Insect Vectors / parasitology
  • Oocysts
  • Plasmodium falciparum / classification
  • Plasmodium falciparum / genetics
  • Plasmodium falciparum / isolation & purification*
  • Plasmodium vivax / classification
  • Plasmodium vivax / genetics
  • Plasmodium vivax / isolation & purification*
  • Protozoan Proteins / blood*
  • Protozoan Proteins / isolation & purification*
  • RNA, Ribosomal, 18S / genetics
  • Real-Time Polymerase Chain Reaction / methods*
  • Sensitivity and Specificity

Substances

  • Antigens, Protozoan
  • DNA, Protozoan
  • Protozoan Proteins
  • RNA, Ribosomal, 18S
  • circumsporozoite protein, Protozoan