文献类型：期刊文献

中文题名：溶藻弧菌诱导凡纳滨对虾消减文库的构建及其表达序列标签分析

英文题名：CONSTRUCTION OF SUBSTRACTED cDNA LIBRARY OF LITOPENAEUS VANNAMEI INDUCED BY VIBRIO ALGINOLYTICUS AND ANALYSIS OF EXPRESSED SEQUENCE TAGS

作者：蔡小辉[1];鲁义善[1];吴灶和[1];简纪常[1];王蓓[1];蔡双虎[1]

机构：[1]广东海洋大学水产学院,广东省水产经济动物病原生物学及流行病学重点试验室暨广东省教育厅水产经济动物病害控制重点实验室,湛江524025

年份：2010

期号：1

起止页码：157

中文期刊名：水生生物学报

外文期刊名：Acta Hydrobiologica Sinica

收录：CSTPCD、、CSCD2011_2012、北大核心2008、北大核心、CSCD

基金：广东省科技计划项目(2005B20301008)资助

语种：中文

中文关键词：凡纳滨对虾;溶藻弧菌;抑制消减杂交(SSH);表达序列标签(EST)

外文关键词：Litopenaeus vannamei; Vibrio alginolyticus; Suppression subtractive hybridization （SSH）; Expressed sequence tag （EST）

中文摘要：利用抑制消减杂交技术构建了溶藻弧菌(Vibrio alginolyticus)诱导的凡纳滨对虾(Litopenaeus vannamei)血淋巴细胞cDNA文库。用DNAMAN5.2.2软件对560条高质量的ESTs进行聚类,共获得239个Unigenes。与GenBank进行BLASTx和BLASTn同源比较,其中66.9%为已知功能基因,33.1%为未知功能基因,GO分类将其分为7类,包括能量和基础代谢类相关的基因为第一大类占36%,免疫相关基因占15%,其他基因占8%,信号转导类占3%,抗氧化酶和凋亡相关蛋白均为2%,核蛋白类占1%。实验结果表明凡纳滨对虾在溶藻弧菌诱导下可产生一系列特异基因的表达,通过对文库的分析显示,基于PCR方法建立的SSH文库为取得大量免疫相关基因的ESTs序列提供了可能。

外文摘要：Vibrio alginolyticus is one of the main causative agents resulting in serious infectious diseases of Litopenaeus vannamei and other animals. Suppression subtractive hybridization （SSH） is a new and highly effective method for analysing differentially expressed or tissue-specific cDNA probes and libraries. It is applicable to diagnosis of disease, development, tissue specificity, or other differential expressing. Based on the user manual of Clontech PCR-SelectTM cDNA subtraction kit, a suppression subtraction cDNA libraries of Litopenaeus vannamei were made by a PCR method. Experimental shrimp were injected with 5×10^7CFU live Vibrio alginolyticus and the control shrimp were injected with steriled normal saline. The mRNA from hemocytes of normal shrimp and vibrio-challenging shrimp must be isolated firstly. After mRNA was reverse transcribed into double strand cDNA, the two kinds of ds cDNA were denominated with Driver cDNA （normal shrimp） and Tester cDNA （vibrio challenging shrimp） separately. Then they were digested with Rsa I at the same time but only Tester ds cDNA were diluted and ligated to adaptor l and adaptor 2R in separate ligation reactions in the same total volume. Then an excess of driver cDNA was added to each tester cDNA for the first round of hybridization to enrich for differentially expressed sequences. Secondly, the two samples from the first hybridization were mixed together and freshly denatured driver DNA was added to each tester cDNA for differentially expressed sequences. Only the remaining normalized and subtracted ss tester cDNA were able to reassociate and form newly hybrids with different adaptors at their 5＇-ends in the second hybridization. The new hybrids were preferentially amplified by PCR with a pair of primers, nested PCR primer 1 and nested PCR primer 2R. Litopenaeus vannamei β-actin gene was used as internal control to estimate the efficiency of subtractive successfully constructed. In this library, β-actin was subtracted significantly above 10 cycles, suggesting that the subtractive cDNA library was successfully constructed. The substracted products were cloned into the pMD-T 18 Vector. Then the recombinated plasmid was transformed into DH5α. PCR analysis showed that the inserts were 488bp equally in length. The subtracted cDNA library including 2000 clones and picked 600 clones to sequence randomly. The obtained 560 ESTs were assembled to 239 Unigenes （164 contigs and 75 singletons） with DNAMAN 5.2.2 software. Compared with sequences in unigene database of GeneBank with BLASTx and BLASTn algorithm, 159 ESTs of them had comparatively clear results and the percent of them in acquired ESTs was 66.9%. The sequences of these ESTs were subjected to GO annotation. According to their physioligical function, they could be subdivided into 7 categories, 36% were metabolism genes; 15% were immune-related genes; 8% were others genes; 3% were regulation and signal transaction factors; 2% were apoptotic-related proteins and antioxidant enzyme; 1% were ribosomal proteins. The result showed that Litopenaeus vannamei, induced by Vibrio alginolyticus, could express serials of special genes. Analysis of the libraries indicates the PCR based suppression subtraction cDNA libraries is feasible used to discover the immune gene in shrimp.