4.8 Article

Small-Molecule Agonists of Ae. aegypti Neuropeptide Y Receptor Block Mosquito Biting

Journal

CELL
Volume 176, Issue 4, Pages 687-+

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2018.12.004

Keywords

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Funding

  1. Robertson Therapeutic Development Fund by the Robertson Foundation
  2. National Center for Advancing Translational Sciences (NCATS) [UL1 TR000043]
  3. NIH Clinical and Translational Science Award (CTSA) program
  4. NIDCD [R01 DC014247]
  5. Rockefeller University Women & Science Fellowship
  6. APS Postdoctoral Fellowship in Biological Science from the American Philosophical Society

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Female Aedes aegypti mosquitoes bite humans to obtain blood to develop their eggs. Remarkably, their strong attraction to humans is suppressed for days after the blood meal by an unknown mechanism. We investigated a role for neuropeptide Y (NPY)-related signaling in long-term behavioral suppression and discovered that drugs targeting human NPY receptors modulate mosquito host-seeking. In a screen of all 49 predicted Ae. aegypti peptide receptors, we identified NPY-like receptor 7 (NPYLR7) as the sole target of these drugs. To obtain small molecule agonists selective for NPYLR7, we performed a high-throughput cell-based assay of 265,211 compounds and isolated six highly selective NPYLR7 agonists that inhibit mosquito attraction to humans. NPYLR7 CRISPR-Cas9 null mutants are defective in behavioral suppression and resistant to these drugs. Finally, we show that these drugs can inhibit biting and blood-feeding on a live host, suggesting a novel approach to control infectious disease transmission by controlling mosquito behavior.

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