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磷酸丙糖异构酶(TPI)促进对虾白斑综合征病毒在脊尾白虾中的复制。

Triosephosphate isomerase (TPI) facilitates the replication of WSSV in Exopalaemon carinicauda.

作者信息

Liu Fei, Li Shihao, Liu Guangxing, Li Fuhua

机构信息

Key Laboratory of Marine Environment and Ecology, Ministry of Education, Ocean University of China, Qingdao 266100, China; Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China.

Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China.

出版信息

Dev Comp Immunol. 2017 Jun;71:28-36. doi: 10.1016/j.dci.2017.01.018. Epub 2017 Jan 23.

Abstract

Triosephosphate isomerase (TPI) is a vital enzyme in the glycolytic pathway, which can catalyze the interconversion of glyceraldehyde-3-phosphate (GAP) and dihydroxyacetone phosphate (DHAP). DHAP is involved in lipid metabolism and phospholipid synthesis. In order to know the role of TPI in WSSV infection to prawn, we cloned the full length cDNA of triosephosphate isomerase gene (EcTPI) from Exopalaemon carinicauda, and its function during WSSV infection was analyzed. EcTPI transcripts were widely distributed in all tissues, but showed relatively higher expression levels in the gill and epidermis. Its expression was apparently up-regulated after 24 h post WSSV injection (hpi), when the virus load began to rise. Furthermore, we detected the expressions of the key genes encoding the enzymes which catalyze the key steps in the glycolysis during WSSV infection. The data showed that genes encoding the enzymes which catalyzed upper steps of glycolysis to produce GAP, including hexokinase (HK), glucose-6-phosphate isomerase (GPI) and phosphofructokinase-1 (PFK-1), were significantly up-regulated at 24 and 27 hpi. Genes encoding the enzymes catalyzing down steps of glycolysis after GAP, including glyceraldehyde-3-phosphate dehydrogenase (GAPDH), enolase (ENO) and pyruvate kinase (PK), were apparent down-regulated at 24 and 27 hpi. Meanwhile, the gene encoding the enzyme glycerol-3-phosphate dehydrogenase (GPDH) catalyzing DHAP to glycerol-3-phosphate (G-3-P) showed down-regulation at 12-27 hpi, while the gene encoding dihydroxyacetone-phosphate acyltransferase (DHAPAT) catalyzing DHAP to further synthesis of phospholipids showed up-regulation at 12-24 hpi. These data suggested that WSSV infection could change the glycolysis pathway to make them produce more phospholipids which could be very helpful for virus replication. In order to further confirm the above speculation, dsRNA interference (RNAi) approach was used to knock down EcTPI gene and analyze its effect on WSSV load in prawn. The data showed that interference of EcTPI gene led to a significant decrease of WSSV loads in WSSV infected prawn. These data provided useful information to understand the infection mechanism of WSSV.

摘要

磷酸丙糖异构酶(TPI)是糖酵解途径中的一种关键酶,它能够催化磷酸甘油醛(GAP)和磷酸二羟丙酮(DHAP)之间的相互转化。DHAP参与脂质代谢和磷脂合成。为了了解TPI在对虾感染白斑综合征病毒(WSSV)过程中的作用,我们克隆了脊尾白虾磷酸丙糖异构酶基因(EcTPI)的全长cDNA,并分析了其在WSSV感染过程中的功能。EcTPI转录本广泛分布于所有组织中,但在鳃和表皮中的表达水平相对较高。在注射WSSV后24小时(hpi),当病毒载量开始上升时,其表达明显上调。此外,我们检测了在WSSV感染期间催化糖酵解关键步骤的酶的关键基因的表达。数据显示,编码催化糖酵解上游步骤以产生GAP的酶的基因,包括己糖激酶(HK)、葡萄糖-6-磷酸异构酶(GPI)和磷酸果糖激酶-1(PFK-1),在24和27 hpi时显著上调。编码在GAP之后催化糖酵解下游步骤的酶的基因,包括磷酸甘油醛脱氢酶(GAPDH)、烯醇化酶(ENO)和丙酮酸激酶(PK),在24和27 hpi时明显下调。同时,编码催化DHAP转化为3-磷酸甘油(G-3-P)的酶甘油-3-磷酸脱氢酶(GPDH)的基因在12 - 27 hpi时下调,而编码催化DHAP进一步合成磷脂的磷酸二羟丙酮酰基转移酶(DHAPAT)的基因在12 - 24 hpi时上调。这些数据表明,WSSV感染可以改变糖酵解途径,使其产生更多对病毒复制非常有帮助的磷脂。为了进一步证实上述推测,采用双链RNA干扰(RNAi)方法敲低EcTPI基因,并分析其对感染WSSV的对虾体内病毒载量的影响。数据显示,干扰EcTPI基因导致感染WSSV的对虾体内病毒载量显著降低。这些数据为了解WSSV的感染机制提供了有用信息。

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