A single fluorescence-based LAMP reaction for identifying multiple parasites in mosquitoes

Exp Parasitol. 2010 Jun;125(2):179-83. doi: 10.1016/j.exppara.2009.12.023. Epub 2010 Jan 11.

Abstract

Vector-borne diseases, such as malaria and lymphatic filariasis, are co-endemic in large parts of the world. To develop a multiplex amplification method for the simultaneous detection of multiple insect-borne infectious diseases, we used LAMP with fluorescently labeled primers to identify the SPECT2 gene of Plasmodium berghei and the cytochrome oxidase subunit I gene of Dirofilaria immitis in mosquitoes. This technique could detect as few as 100 P. berghei-infected red blood cell-equivalents or one D. immitis microfilaria. Moreover, individual species of parasites in mosquitoes could be identified when a mixture of fluorescently labeled primer sets was used. These findings suggest that the multiplex LAMP assay is sensitive and specific enough to identify parasite-bearing mosquitoes in areas where several diseases occur simultaneously. This procedure could increase the efficiency and effectiveness of arthropod-borne disease elimination programs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aedes / parasitology*
  • Animals
  • Anopheles / parasitology*
  • DNA, Helminth / isolation & purification
  • DNA, Protozoan / isolation & purification
  • Dirofilaria immitis / genetics
  • Dirofilaria immitis / isolation & purification*
  • Female
  • Insect Vectors / parasitology*
  • Malpighian Tubules / parasitology
  • Mice
  • Mice, Inbred BALB C
  • Microscopy, Fluorescence
  • Nucleic Acid Amplification Techniques / methods*
  • Nucleic Acid Amplification Techniques / standards
  • Plasmodium berghei / genetics
  • Plasmodium berghei / isolation & purification*
  • Sensitivity and Specificity

Substances

  • DNA, Helminth
  • DNA, Protozoan