School of Natural Sciences, University of California Merced, 5200 N Lake Road, Merced, CA, 95343, USA.
Universidad de Sonora, Departamento de Ciencias Químico-Biológicas y Agropecuarias, Universidad de Sonora Unidad Regional Sur, Apartado Postal 85880, Navojoa, Sonora, Mexico.
Fish Shellfish Immunol. 2019 Sep;92:165-171. doi: 10.1016/j.fsi.2019.05.040. Epub 2019 May 27.
Hypoxia-inducible factor -1 (HIF-1) is a transcriptional factor that regulates the expression of several glycolytic genes. The white spot syndrome virus (WSSV) induces a shift in glycolysis that favors viral replication in white shrimp Litopenaeus vannamei. HIF-1 is related to the pathogenesis of the WSSV infection through the induction of metabolic changes in infected white shrimp. Although the WSSV infection is associated with metabolic changes, the role of HIF-1 on key glycolytic genes during the WSSV infection has not been examined. In this work, we evaluated the effect of HIF-1α silencing on expression and activity of glycolytic enzymes (Hexokinase-HK, phosphofructokinase-PFK and pyruvate kinase-PK) along with the glucose transporter 1 (Glut1), regulatory enzymes (glucose-6-phosphate dehydrogenase-G6PDH and pyruvate dehydrogenase-PDH), and metabolic intermediates of glycolysis (glucose-6-phosphate-G6P and pyruvate). The expression of Glut1 increased in each tissue evaluated after WSSV infection, while HK, PFK and PK gene expression and enzyme activities increased in a tissue-specific manner. G6PDH activity increased during WSSV infection, and its substrate G6P decreased, while PDH activity decreased and its substrate pyruvate increased. Silencing of HIF-1α blocked the WSSV-induced Glut1 and glycolytic genes upregulation and enzyme activity in a tissue-specific manner. We conclude that HIF-1 regulates the WSSV-induced glycolysis through induction of glycolytic genes contributing to glucose metabolism in tissues of infected shrimp. Also, the inhibition, and activation of regulatory genes are likely to decrease the availability of the raw materials essential for WSSV replication and increase oxidative metabolism.
缺氧诱导因子-1(HIF-1)是一种转录因子,可调节几种糖酵解基因的表达。白斑综合征病毒(WSSV)诱导糖酵解发生转变,有利于白对虾(Litopenaeus vannamei)中病毒的复制。HIF-1通过诱导感染白对虾的代谢变化与 WSSV 感染的发病机制有关。尽管 WSSV 感染与代谢变化有关,但在 WSSV 感染期间,HIF-1 对关键糖酵解基因的作用尚未得到研究。在这项工作中,我们评估了 HIF-1α 沉默对糖酵解酶(己糖激酶-HK、磷酸果糖激酶-PFK 和丙酮酸激酶-PK)以及葡萄糖转运蛋白 1(Glut1)、调节酶(葡萄糖-6-磷酸脱氢酶-G6PDH 和丙酮酸脱氢酶-PDH)的表达和活性的影响,以及糖酵解的代谢中间产物(葡萄糖-6-磷酸-G6P 和丙酮酸)。WSSV 感染后,每种组织中 Glut1 的表达均增加,而 HK、PFK 和 PK 基因的表达和酶活性则以组织特异性的方式增加。G6PDH 活性在 WSSV 感染期间增加,其底物 G6P 减少,而 PDH 活性降低,其底物丙酮酸增加。HIF-1α 的沉默以组织特异性的方式阻断了 WSSV 诱导的 Glut1 和糖酵解基因的上调以及酶活性。我们得出结论,HIF-1 通过诱导糖酵解基因的表达来调节 WSSV 诱导的糖酵解,从而促进感染虾组织中的葡萄糖代谢。此外,调节基因的抑制和激活可能会降低病毒复制所需的原材料的可用性,并增加氧化代谢。