Isoe Jun, Petchampai Natthida, Isoe Yurika E, Co Katrina, Mazzalupo Stacy, Scaraffia Patricia Y
Department of Chemistry and Biochemistry, University of Arizona, Tucson, Arizona, USA.
Department of Tropical Medicine, Vector-Borne Infectious Disease Research Center, School of Public Health and Tropical Medicine, Tulane University, New Orleans, Louisiana, USA.
FASEB J. 2017 Jun;31(6):2276-2286. doi: 10.1096/fj.201601185R. Epub 2017 Feb 8.
has 2 genes encoding xanthine dehydrogenase (XDH). We analyzed and gene expression by real-time quantitative PCR in tissues from sugar- and blood-fed females. Differential and gene expression was observed in tissues dissected throughout a time course. We next exposed females to blood meals supplemented with allopurinol, a well-characterized XDH inhibitor. We also tested the effects of injecting double-stranded RNA (dsRNA) against XDH1, XDH2, or both. Disruption of XDH by allopurinol or XDH1 by RNA interference significantly affected mosquito survival, causing a disruption in blood digestion, excretion, oviposition, and reproduction. XDH1-deficient mosquitoes showed a persistence of serine proteases in the midgut at 48 h after blood feeding and a reduction in the uptake of vitellogenin by the ovaries. Surprisingly, analysis of the fat body from dsRNA-XDH1-injected mosquitoes fell into 2 groups: one group was characterized by a reduction of the XDH1 transcript, whereas the other group was characterized by an up-regulation of several transcripts, including XDH1, glutamine synthetase, alanine aminotransferase, catalase, superoxide dismutase, ornithine decarboxylase, glutamate receptor, and ammonia transporter. Our data demonstrate that XDH1 plays an essential role and that XDH1 has the potential to be used as a metabolic target for vector control.-Isoe, J., Petchampai, N., Isoe, Y. E., Co, K., Mazzalupo, S., Scaraffia, P. Y. Xanthine dehydrogenase-1 silencing in mosquitoes promotes a blood feeding-induced adulticidal activity.
有2个编码黄嘌呤脱氢酶(XDH)的基因。我们通过实时定量PCR分析了取食糖水和血液的雌性蚊子组织中的 和 基因表达。在整个时间进程中解剖的组织中观察到了 和 基因的差异表达。接下来,我们让雌性蚊子取食添加了别嘌呤醇(一种特征明确的XDH抑制剂)的血液。我们还测试了注射针对XDH1、XDH2或两者的双链RNA(dsRNA)的效果。别嘌呤醇破坏XDH或RNA干扰破坏XDH1均显著影响蚊子的存活,导致血液消化、排泄、产卵和繁殖受到干扰。缺乏XDH1的蚊子在取食血液48小时后中肠中丝氨酸蛋白酶持续存在,卵巢对卵黄原蛋白的摄取减少。令人惊讶的是,对注射dsRNA-XDH1的蚊子脂肪体的分析分为两组:一组的特征是XDH1转录本减少,而另一组的特征是包括XDH1、谷氨酰胺合成酶、丙氨酸转氨酶、过氧化氢酶、超氧化物歧化酶、鸟氨酸脱羧酶、谷氨酸受体和氨转运体在内的几种转录本上调。我们的数据表明,XDH1起着至关重要的作用,并且XDH1有潜力被用作病媒控制的代谢靶点。-伊索,J.,佩昌派,N.,伊索,Y.E.,科,K.,马扎卢波,S.,斯卡拉菲亚,P.Y.蚊子中黄嘌呤脱氢酶-1沉默促进血液摄取诱导的成虫杀灭活性。