Repurposing isoxazoline veterinary drugs for control of vector-borne human diseases.

Marie Miglianico, Maarten Eldering, Hannah Slater, Neil Ferguson, Pauline Ambrose, Rosemary Lees, Karin M.J. Koolen, Katerina Pruzinova, Magdalena Jancarova, Petr Volf, Constantianus J.M. Koenraadt, Hans Peter Duerr, Graham Trevitt, Baiyuan Yang, Arnab K. Chatterjee, John Wisler, Angelika Sturm, Teun Bousema, Robert W. Sauerwein, Peter G. SchultzMatthew S. Tremblay, Koen J. Dechering

Research output: Contribution to journalArticlepeer-review

68 Citations (Scopus)

Abstract

Isoxazolines are oral insecticidal drugs currently licensed for ectoparasite control in companion animals. Here we propose their use in humans for the reduction of vector-borne disease incidence. Fluralaner and afoxolaner rapidly killed , , and mosquitoes and sand flies after feeding on a drug-supplemented blood meal, with IC values ranging from 33 to 575 nM, and were fully active against strains with preexisting resistance to common insecticides. Based on allometric scaling of preclinical pharmacokinetics data, we predict that a single human median dose of 260 mg (IQR, 177-407 mg) for afoxolaner, or 410 mg (IQR, 278-648 mg) for fluralaner, could provide an insecticidal effect lasting 50-90 days against mosquitoes and sand flies. Computational modeling showed that seasonal mass drug administration of such a single dose to a fraction of a regional population would dramatically reduce clinical cases of Zika and malaria in endemic settings. Isoxazolines therefore represent a promising new component of drug-based vector control.

Original languageEnglish
Pages (from-to)e6920-e6926
JournalProceedings of the National Academy of Sciences of the United States of America
Volume115
Issue number29
Early online date2 Jul 2018
DOIs
Publication statusPublished - 17 Jul 2018

Keywords

  • Insecticide
  • Isoxazoline
  • Malaria
  • Vector control
  • Zika fever

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