Piermarini Peter M, Esquivel Carlos J, Denton Jerod S
Department of Entomology, Ohio Agricultural Research and Development Center, The Ohio State University, Wooster, OH 44691, USA.
Departments of Anesthesiology and Pharmacology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Int J Environ Res Public Health. 2017 Jan 24;14(2):111. doi: 10.3390/ijerph14020111.
The Malpighian tubules and hindgut are the renal excretory tissues of mosquitoes; they are essential to maintaining hemolymph water and solute homeostasis. Moreover, they make important contributions to detoxifying metabolic wastes and xenobiotics in the hemolymph. We have focused on elucidating the molecular mechanisms of Malpighian tubule function in adult female mosquitoes and developing chemical tools as prototypes for next-generation mosquitocides that would act via a novel mechanism of action (i.e., renal failure). To date, we have targeted inward rectifier potassium (Kir) channels expressed in the Malpighian tubules of the yellow fever mosquito and malaria mosquito . Inhibition of these channels with small molecules inhibits transepithelial K⁺ and fluid secretion in Malpighian tubules, leading to a disruption of hemolymph K⁺ and fluid homeostasis in adult female mosquitoes. In addition, we have used next-generation sequencing to characterize the transcriptome of Malpighian tubules in the Asian tiger mosquito , before and after blood meals, to reveal new molecular targets for potentially disrupting Malpighian tubule function. Within 24 h after a blood meal, the Malpighian tubules enhance the mRNA expression of genes encoding mechanisms involved with the detoxification of metabolic wastes produced during blood digestion (e.g., heme, NH₃, reactive oxygen species). The development of chemical tools targeting these molecular mechanisms in Malpighian tubules may offer a promising avenue for the development of mosquitocides that are highly-selective against hematophagous females, which are the only life stage that transmits pathogens.
马尔皮基氏小管和后肠是蚊子的肾脏排泄组织;它们对于维持血淋巴中的水分和溶质稳态至关重要。此外,它们在清除血淋巴中的代谢废物和外源性物质方面也发挥着重要作用。我们致力于阐明成年雌性蚊子马尔皮基氏小管功能的分子机制,并开发化学工具作为下一代杀蚊剂的原型,这些杀蚊剂将通过一种新的作用机制(即肾衰竭)发挥作用。迄今为止,我们已将目标对准在黄热病蚊子和疟蚊的马尔皮基氏小管中表达的内向整流钾(Kir)通道。用小分子抑制这些通道会抑制马尔皮基氏小管中的跨上皮钾离子和液体分泌,导致成年雌性蚊子血淋巴中的钾离子和液体稳态受到破坏。此外,我们利用下一代测序技术对亚洲虎蚊在吸血前后马尔皮基氏小管的转录组进行了表征,以揭示可能破坏马尔皮基氏小管功能的新分子靶点。在吸血后24小时内,马尔皮基氏小管会增强参与消化血液过程中产生的代谢废物(如血红素、氨、活性氧)解毒机制的基因的mRNA表达。开发针对马尔皮基氏小管中这些分子机制的化学工具可能为开发对吸血雌性蚊子具有高度选择性的杀蚊剂提供一条有前景的途径,因为吸血雌性蚊子是唯一传播病原体的生命阶段。