2014, 21(4):0.
摘要:Tilapia is one of the most extensively cultured species in aquaculture with great economic importance, and has been introduced to nearly 100 countries in the world. China is the biggest country in tilapia production, accounting for about 55% of the total production in the world. In which, Nile tilapia () has played an important role in developing tilapia industry. Since 1978, Nile tilapia first introduced to China, it has been multiply introduced from different countries or areas for several times. Consequently a number of domesticated strains or populations have been established and developed with different selective pressures and divergent genetic characteristics in China. This gives us a chance to combine multiple germplasm resources in breeding practices of tilapia. However, the genetic evaluation and investigation of these domesticated populations of Nile tilapia in China have been relatively poorly conducted. In this study, genetic diversity and genetic relationships of the eight domesticated populations of Nile tilapia in China were examined using partial mitochondrial control region (D-loop) sequence, including the Egypt (EGY), Gilada (GLD), American (USA), Luye (LY), Genomar (GNM), Baolu (BL), Guangdong (GD) and New GIFT (NGF) populations. The results showed that only 15 haplotypes were defined in the 237 analyzed individuals, in which, BL1 haplotype was shared by the five populations (BL, EGY, GLD, GNM, LY), but no one shared haplotype was found for all the populations. The Number of variable sites (), haplotype diversity () and 4 to 83, 0.50 to 37.26, 0.190 8 to 0.802 3 and0.000 8 to 0.056 9, respectively. The genetic diversity in the LY was the lowest in the eight populations analyzed. The results of analysis of molecular variance (AMOVA) indicated significant genetic divergence (<0.01) among the populations. The cluster analysis based on Kimura two-parameter model exhibited the two clusters among them, one cluster included the three populations of BL, GD and NGF, and another cluster consisted of the five populations of EGY, LY, GNM, GLD and USA. However, it was not well supported by the haplotype network profile in network. This study provided insight into the genetic basis of Nile tilapia in combining their germplasm in future
2014, 21(4):0.
摘要:首先在凡纳滨对虾(Litopenaeus vannamei)转录组测序的基础上, 应用RT-PCR方法获得了凡纳滨对虾泛素交联酶E2 (UE2)基因的开放阅读框序列。该序列长为447 bp, 编码148个氨基酸, 理论相对分子量为16.84 kD, 等电点为4.90。同源性比对和系统进化分析显示, 不同物种的UE2基因具有较高的同源性, 其中凡纳滨对虾与中国明对虾(Fenneropenaeus chinensis)的同源性最高并聚为一支。半定量RT-PCR分析表明, UE2基因在所检测的组织中均有表达; 实时定量PCR分析表明, UE2基因在肝胰腺和肠中的表达量最高, 在心脏、鳃、胃和肌肉组织中的表达量略低, 在血淋巴中的表达量最低。原核表达分析结果显示, PCR®T7/NT-Topo TA-UE2表达载体在1.0 mmol/L IPTG、37℃诱导3 h条件下可获得纯度较高的分子量约17 kD的蛋白。利用亲和层析的方法将蛋白进行纯化用以制备抗体。研究结果将为深入研究UE2基因在对虾白斑综合症病毒侵染过程中的作用机制奠定基础。
2014, 21(4):0.
摘要:大鲵虹彩病毒是近年中国大陆新发现的引起人工养殖大鲵Andrias davidianus大规模死亡的病毒病原。为了揭示大鲵虹彩病毒流行株的基因型差异本研究对年采集自全国不同大鲵养殖区域的患虹彩病毒病的大鲵样本进行了分子检测、病毒分离培养以及病毒主衣壳蛋白基因测序与比对分析。结果显示采自陕西、湖北、湖南、浙江、江西、福建等省的个样本检测为阳性通过细胞培养获得株病毒流行株。对该株流行株基因的测序与比对分析发现核苷酸序列相似性达到其推测的氨基酸序列无明显差异证实中国大鲵虹彩病毒流行株属同一基因型。所选大鲵虹彩病毒与蛙病毒分别聚为一枝但其亲缘关系较近。本研究结果旨为大鲵虹彩病毒病的疫苗研制及其免疫防控技术研究奠定基础。
2014, 21(4):0.
摘要:、、不同组织之间甲基化水平差异显著。太平洋牡蛎中存在组织特异性甲基化片段和非组织特异性甲基化片段这可能与牡蛎较高的杂合度相关。对实验样品进行的荧光标记的扩增片段长度多态性基于以上结果可以推测基因组甲基化水平可能与个体遗传背景相关联。
2014, 21(4):655-661.
2014, 21(4):720-728.
摘要:(025.12 mmol/L63.10 mmol/L))方正鲫和大鳞鲃精子的激烈运动时间、快速运动时间和寿命最长(48.91±1.43) s(102.16±8.82) s8盐度大于方正鲫和大鳞鲃精子死亡盐度大于松浦镜鲤精子死亡。种鱼的精子激烈运动时间、快速运动时间和寿命均最长时63.0%372.3%, , 分别为和
2014, 21(4):747-758.
摘要:), 4 h12 h48 h96 h14 d, 种组织中白介素细胞表面受体细胞表面受体, 基因的表达高峰出现时间在2~703TNFα表达高峰出现在在头肾和鳃中表达高峰出现在7 d, IgM各基因表达最高值, 且脾、头肾中表达量最高值出现时间早于浸泡组
2014, 21(4):759-768.
摘要:carpio haematopterus]攻毒后的抵抗能力。选择体质量为1 80012350Ⅶ–Ⅻ750 mg/kg(Ⅱ–Ⅵ150 mg750 mg β-)42 d14, 502550 14 d。结果表明葡聚糖均显著提高黄河鲤的活性和PI, , 葡聚糖对黄河鲤的产生抑制效应LZM但是注射高剂量的组对比中等剂量组偏低。攻毒实验显示葡聚糖剂量在, 85.46±7.71, RPS92.96±2.89