Zeledon Emely V, Baxt Leigh A, Khan Tanweer A, Michino Mayako, Miller Michael, Huggins David J, Jiang Caroline S, Vosshall Leslie B, Duvall Laura B
Laboratory of Neurogenetics and Behavior, The Rockefeller University, New York NY 10065, USA.
Howard Hughes Medical Institute, New York NY 10065, USA.
bioRxiv. 2024 Mar 5:2024.02.28.582529. doi: 10.1101/2024.02.28.582529.
Female mosquitoes can spread disease-causing pathogens when they bite humans to obtain blood nutrients required for egg production. Following a complete blood meal, host-seeking is suppressed until eggs are laid. Neuropeptide Y-like Receptor 7 (NPYLR7) plays a role in endogenous host-seeking suppression and previous work identified small molecule NPYLR7 agonists that suppress host-seeking and blood feeding when fed to mosquitoes at high micromolar doses. Using structure activity relationship analysis and structure-guided design we synthesized 128 compounds with similarity to known NPYLR7 agonists. Although potency (EC) was not strictly predictive of effect, we identified 3 compounds that suppressed blood feeding from a live host when fed to mosquitoes at a 1 μM dose, a 100-fold improvement over the original reference compound. Exogenous activation of NPYLR7 represents an innovative vector control strategy to block mosquito biting behavior and prevent mosquito/human host interactions that lead to pathogen transmission.
雌性蚊子在叮咬人类以获取产卵所需的血液营养时,能够传播致病病原体。在饱餐一顿血液后,寻找宿主的行为会受到抑制,直到产卵。神经肽Y样受体7(NPYLR7)在内源性寻找宿主行为抑制中发挥作用,先前的研究确定了小分子NPYLR7激动剂,当以高微摩尔剂量喂给蚊子时,这些激动剂会抑制寻找宿主和吸血行为。利用构效关系分析和结构导向设计,我们合成了128种与已知NPYLR7激动剂相似的化合物。尽管效力(EC)并不能严格预测效果,但我们确定了3种化合物,当以1μM的剂量喂给蚊子时,它们能抑制从活体宿主获取血液,比原始参考化合物有100倍的改善。NPYLR7的外源性激活代表了一种创新的病媒控制策略,可阻止蚊子的叮咬行为,并防止导致病原体传播的蚊子/人类宿主相互作用。