773 resultados para Fenneropenaeus indicus


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The study was undertaken to ascertain the commercially important species of penaeid prawns caught in Batan Bay, Philippines and their abundance in fish corrals. A total of 12 species were commercially caught: Penaeus monodon, P. semisulcatus, P. merguiensis, P. indicus, P. latisulcatus, P. japonicus, P. canaliculatus, Metapenaeus ensis, M. endeavouri, M. dalli, M. elegans, and Trachypenaeus fulvus.

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Dynamics of penaeid postlarval ingression and settlement in the backwaters of Cochin were studied. Postlarval recruits were constituted by Metapenaeus dobsoni (70.8-78.4%), Penaeus indicus (17.5-24.6%), M. monoceros (3.8-4.6%) and P. monodon (0.3-0.4%). Their composition varied with location and season. Postlarval abundance and ingression were influenced by diel, tidal, lunar and seasonal factors. Ingression is mainly nocturnal in all species with nearly 84% of the activity during night hours. Abundance and ingression peaked up during high tides at night with major peaks coinciding with spring tides of full and new moon. It also followed a generalized seasonal pattern with two well-defined peaks for all species. It was pre-monsoon followed by post-monsoon for P. indicus and M. monoceros and post-monsoon followed by pre-monsoon for M. dobsoni. Sizes of the recruits were relatively small during pre-monsoon and post-monsoon and large during monsoon.

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Previously an asteroid starfish Astropecten indicus has been described by Tahera (1996), and another species of the genus Astropecten i.e. A. polyacanthus Muller and Troschel, 1842 has been collected from the subtidal region of a sandy shore of Clifton (24°47'42"N 66°59'6"E), Karachi. The latter species is here reported for the first time from the Pakistan coast of the northern Arabian Sea and fills the gap in the known distribution. The species is briefly described and illustrated.

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This project was done for identifying the mesopelagic fish of the Iranian waters of Oman Sea, during two year from 2008 to 2010. The specimens were collected using two trawler vessel from nine station. All the specimens were fixed in formalin then in 70% alcohol and carried to the laboratory. In total of 19 species belonged to 14 families of 6 orders identified including: Echinorhinidae, Stomidae, Phosichthyidae, Synodontidae, Paralepididae, Myctophidae, Acropomatidae, Priacanthidae, Pentacerotidae, Champsodontidae, Gempylidae, Trichiuridae, Nomeidae and Congridae. Of which 17 species were identified up to species level including: Echinorhinus brucus, Bathophilus indicus, Chauliodus sloani, Harpadon nehereus, Lestrolepis japonica, Benthosema pterotum, Diaphus garmani, Diaphus effulgens, Bolinichthys photothorax, Acropoma japonicum, Synagrops adeni, Cookeolus boops, Histiopterus typus, Champsodon sagittus, Neoepinnula orientalis, Trichiurus lepturus, Cubiceps baxteri. Vinciguerria was identified up to genus level because only one specimen caught during the survey and one species (Congridae) was identified up to family level because only 3 specimens of this fish in early stage of life were caught and their characters were not suitable for identify up to species level. The highest species belong to Myctophidae family of Myctophiformes order.

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The phylogenetic relationships within the family Penaeidae are examined based on mitochondrial 16S rRNA gene sequence analysis of 30 species from 20 genera. The analysis generally supports the three- tribe scheme proposed by Burkenroad ( 1983) but it is not consistent with the five- group classification of Kubo ( 1949). Three clades are resolved: ( Penaeus sensu stricto + Fenneropenaeus + Litopenaeus + Farfantepenaeus + Marsupenaeus + Melicertus + Funchalia + Heteropenaeus), ( Metapenaeus + Parapenaeopsis + Xiphopenaeus + Rimapenaeus + Megokris + Trachysalambria) and ( Metapenaeopsis + Penaeopsis + Parapenaeus), corresponding to the Penaeini, Trachypenaeini and Parapenaeini respectively, while the affinities of Atypopenaeus and Trachypenaeopsis are obscure. The molecular data support that Miyadiella represents the juvenile stage of Atypopenaeus. Within the Trachypenaeini, Trachypenaeus sensu lato is clearly paraphyletic, while the monophyly of Penaeus sensu lato in the Penaeini is questionable.

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Penaeidins, members of a new family of antimicrobial peptides constitutively produced and stored in the haemocytes of penaeid shrimp, display antimicrobial activity against bacteria, and fungi. Here, a DNA sequence encoding the mature Ch-penaeidin peptide was cloned into the pPIC9K vector and transformed into Pichia pastoris. The transformed cells were screened for multi-copy plasmids using increasing concentrations of G418. Positive colonies carrying chromosomal integrations of the Chp gene were identified by phenotype and PCR. When transformed cells were induced with methanol, SDS-PAGE and Western blotting revealed the production of a similar to6100 Da recombinant CHP (rCHP) expression product. Large scale expression revealed that rCHP was produced at 108 mg/L under optimal conditions in the highest Chp-producing P. pastoris clone. The antimicrobial activities of rCHP were studied by liquid phase analysis, which revealed that rCHP exhibited activities against some Gram-negative and Gram-positive bacteria, but had a relatively low activity against some fungi. Purification of rCHP by cation exchange chromatography and subsequent automated amino acid sequencing revealed the presence of four additional amino acids (YVEF) at the N-terminus that belonged to the cleaved fusion signal peptide; these residues may account for the observed decrease in antifungal activity. Together, these observations indicate that rCHP is an effective antimicrobial peptide that can be successfully produced at high levels in the yeast, and therefore may be a potential antimicrobial candidate for practical use. (C) 2004 Elsevier Inc. All rights reserved.

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Genetic differentiation of the shrimp Penaeus chinensis in the Yellow Sea and Bohai Sea was investigated using the mitochondrial control region (CR). RFLP of a partial CR segment (613 bp) shows that 106 out of 122 (86.9%) individuals from six sampling localities along the coast of northern China and the west coast of the Korean Peninsula share the same haplotype, and the haplotype frequencies among localities are not significantly different. The findings are further confirmed by sequencing the complete CR. Divergence of the complete CR (992 bp) is less than 1.6% in 14 individuals from the six localities. F-statistics based on RFLP data and the TCS network of sequencing data suggest little genetic differentiation of P. chinensis in the Yellow Sea and Bohai Sea. Mismatch analysis suggests a rapid expansion of P. chinensis population to the Yellow Sea and the Bohai Sea, which probably occurred with the rapid rise in sea level after the last glacial maximum. Despite the lack of genetic heterogeneity, we propose that P. chinensis populations in this region should be treated as separate management units, as fishery management programs have to be applied on a local basis by different governments.

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A crustin-like protein (CruFc) from Fenneropenaeus chinensis was expressed in Pichia pastoris and then purified to electrophoretic homogeneity on a Sephacryl S-100 column with a band corresponding to the expected one (13 kDa) shown by 15% SDS-PAGE. Western blot indicated that the rCruFc specifically reacted with polyclonal rabbit anti-Fenneropenaeus chinensis CruFc. Production in a 5 l bioreactor gave 237 mg rCruFc/l. Antimicrobial assay revealed that 4 mu M rCruFc inhibited growth of Staphylococcus aureus.

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Fenneropenaeus chinensis is confined to the Yellow Sea and Bohai Sea in China and the West Coast of the Korean Peninsula. Intra- and intercross populations were produced between Rushany (YP) and Korean (KN) populations. Seven traits were recorded. The heterosis of hybrids was computed and comparison between treatments was performed by ANOVA. At the fourth month after post-larvae, six indexes of growth trait and viability showed a range of heterosis, ranging from 0.514% to 14.950%. At the fifth month after post-larvae, six indexes of growth trait and viability ranged from -9.000% to 19.090%. The negative heterosis was observed in CL, HST and viability. The heterosis of KN female xYP male tended generally to increase as the age of the Chinese shrimp increased while the heterosis of YP female xKN male tended to decrease. The results indicated that the viability of reciprocal hybrids were not significantly different (P > 0.05) from their parents during the experiment. The result of ANOVA indicated that the F1 hybrids were significantly different (P < 0.05) in WST and TW at the fourth month. The multiple comparisons of LSD test indicated that the hybrids of YP female xKN male were significantly different (P < 0.05) from their parents in TW. The hybrids of YP female xKN male were significantly different (P < 0.05) from the other three combinations in WST. At the fifth months, the F1 hybrids had significant difference (P < 0.05) in body weight while other traits showed no significant differences (P > 0.05) from their parents. The multiple comparisons of LSD test indicated that the hybrids of KN female xYP male were significantly different (P < 0.05) from the KN parents in TW. The results indicate that in experimental conditions, the F-1 hybrids created from two populations of Chinese shrimp showed a certain level of heterosis for growth performance and viability. The crossing scheme may improve growth performance and viability in Chinese shrimp, but the improvement may be limited because effective crossbreeding requires the maintenance of pure, preferably inbred, lines and possibly involves specialized sire and dam lines. Therefore, the exploitation of heterosis through single crossbreeding in Chinese shrimp is of limited utility in practical commercial shrimp aquaculture in spite of the potential of significant heterosis. The crossbreeding of different populations can be applied in the establishment of base populations.

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对虾病害在世界范围内的广泛传播,给水产养殖和沿海农村经济造成了重大损失。深入开展对虾免疫机制研究并在此基础上寻找对虾疾病防治的有效方法已成为当务之急。研究表明,当对虾等甲壳动物受到外界病原刺激时,其体内的吞噬细胞在吞噬活动中会激活磷酸己糖支路的代谢,引起呼吸爆发,产生多种活性氧分子。另外,受到病原侵染的对虾还会产生其他多种免疫反应,这些免疫反应将消耗大量的能量(ATP),产能的呼吸链会加速运转,由此也会引发大量活性氧的产生。这些活性氧分子可以杀灭入侵的病原微生物,但同时由于活性氧分子反应的非特异性,它们也会对宿主的细胞、组织和器官造成严重伤害,进而导致对虾生理机能的损伤和免疫系统的破坏。所以,消除对虾体内因过度免疫反应产生的过量氧自由基将能够增强其抵御病原侵染的能力,提高免疫力。本论文从中国明对虾体内克隆了线粒体型超氧化物歧化酶(mMnSOD)、胞质型超氧化物歧化酶(cMnSOD)、过氧化氢酶(Catalase)和过氧化物还原酶(Peroxiredoxin)等四种与免疫系统相关的抗氧化酶基因,分析了它们的分子结构特征,组织分布及应答不同病原刺激的表达变化模式,并对其中的mMnSOD基因和Peroxiredoxin基因进行了体外重组表达、分离纯化和酶活性分析。 采用RACE技术从中国明对虾血细胞中克隆了两个超氧化物歧化酶(SOD)基因,通过序列比对分析发现,其中一个为mMnSOD基因,另一个为cMnSOD基因。mMnSOD基因的cDNA全长为1185个碱基,其中开放阅读框为660个碱基,编码220个氨基酸,其中推测的信号肽为20个氨基酸。多序列比对结果显示中国明对虾mMnSOD基因的推导氨基酸序列与罗氏沼虾、蓝蟹的推导氨基酸序列同源性分别为88%和82%。Northern blot结果表明,该基因在对虾的肝胰脏、血细胞、淋巴器官、肠、卵巢、肌肉和鳃等组织中均有表达。半定量RT-PCR结果显示,对虾感染病毒3 h时,该基因在血细胞和肝胰脏中的转录水平显著升高。此外,通过构建原核表达载体,本研究对该基因进行了体外重组表达,并对纯化的重组蛋白进行了质谱鉴定和酶活分析。cMnSOD基因的cDNA全长为1284个碱基,其中开放阅读框为861个碱基,编码287个氨基酸。多序列比对结果显示中国明对虾cMnSOD基因的推导氨基酸序列与斑节对虾和凡纳滨对虾的同源性高达98%和94%。组织半定量结果显示,cMnSOD基因在对虾被检测的各个组织中均有表达。 另外,半定量RT-PCR结果表明,对虾感染病毒23h时,该基因在肝胰脏中的转录上升到正常水平的3.5倍;而感染后59 h时,该基因在血细胞中的转录上升到正常水平的2.5倍。 利用根据其他生物过氧化氢酶保守氨基酸序列设计的简并引物,结合RACE技术,从中国明对虾肝胰脏中克隆到了过氧化氢酶基因的部分片段,片段长1725个碱基。多序列比对结果发现目前所得中国明对虾Catalase基因部分片段的推导氨基酸序列与罗氏沼虾和皱纹盘鲍Catalase氨基酸序列的同源性分别达到95%和73%。通过实时荧光定量PCR技术对中国明对虾Catalase基因在各个组织中的分布情况及病毒感染后该基因在血细胞和肝胰脏中的转录变化进行了研究。结果发现,该基因在肝胰脏、鳃、肠和血细胞中表达水平较高,在卵巢、淋巴器官和肌肉中的表达水平相对较弱;感染病毒23 h和37 h时,对虾血细胞和肝胰脏中该基因mRNA的表达量分别出现显著性上升。 依据中国明对虾头胸部cDNA文库提供的部分片段信息,结合SMART-RACE技术,从中国明对虾肝胰脏中克隆到了过氧化物还原酶基因(Peroxiredoxin), 该基因的cDNA全长为942个碱基,其中开放阅读框为594个碱基,编码198个氨基酸。中国明对虾Peroxiredoxin基因的推断氨基酸序列与伊蚊、文昌鱼和果蝇等Peroxiredoxin基因的推断氨基酸序列同源性分别为77%、76%和73%。其蛋白理论分子量为22041.17 Da,pI为5.17。Northern blot结果表明,Peroxiredoxin基因在对虾的肝胰脏、血细胞、淋巴器官、肠、卵巢、肌肉和鳃等组织中均有表达。实时荧光定量PCR结果显示,弧菌感染后,该基因在对虾血细胞和肝胰脏中的转录水平都有明显变化并且表达模式不同。另外,对该基因进行了体外重组表达,并对纯化的重组蛋白进行了质谱鉴定和酶活性分析。酶活性分析表明,复性后的重组蛋白能在DTT存在的条件下还原H2O2。

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对虾流行病爆发以来,我国乃至世界的对虾产业一直受到各种虾病的困扰,对虾养殖业严重受阻。解决这一问题的关键是加强对虾免疫机制的研究,并在此基础上寻找对虾疾病防治的有效方法。Rel/NF-κB是一类核转录因子,在无脊椎动物的先天性免疫中,起着极为重要的作用。 本论文根据其他无脊椎动物中NF-κB家族基因Relish和Dorsal的保守氨基酸序列分别设计简并引物,从中国明对虾血细胞cDNA中先后克隆到了Relish和Dorsal基因的部分片段,并结合SMART-RACE技术分别获得了中国明对虾Relish基因(FcRelish)和Dorsal基因(FcDorsal)的cDNA 全长。 FcRelish的cDNA 全长为2157个碱基,其中开放阅读框为1512个碱基,编码504个氨基酸;FcRelish蛋白的推导分子量为57373.5 Da,理论等电点为7.00。FcDorsal基因的cDNA 全长为1627个碱基,其中开放阅读框为1071个碱基,编码357个氨基酸;FcDorsal蛋白的推导分子量为39780.7 Da,理论等电点为8.85。 分析了FcRelish基因和FcDorsal基因的在血细胞、淋巴器官、肠和肌肉等12个组织中的表达水平。组织表达结果表明FcRelish和FcDorsal在淋巴器官和血细胞中表达水平明显高于其他组织,而淋巴器官和血细胞是对虾免疫系统中最重要的两个组织,由此可以推测中国明对虾中的Relish和Dorsal可能与免疫关系密切。 本论文还利用实时荧光定量PCR技术,对灭活鳗弧菌刺激,以及WSSV病毒刺激后,对虾血细胞和淋巴器官中FcRelish基因和FcDorsal基因的转录水平进行了研究。FcRelish基因在WSSV病毒刺激后,在血细胞和淋巴器官中都出现了波浪形变化,说明FcRelish对WSSV病毒刺激产生了应答。在灭活鳗弧菌刺激后,FcRelish在血细胞中变化不明显,而在淋巴器官中出现了两次明显的下调上调交替,出现这种现象的具体原因有待探究。在WSSV病毒刺激后,血细胞和淋巴器官中FcDorsal的转录表达呈波浪形变化。而在鳗弧菌刺激后,FcDorsal在血细胞和淋巴器官中的转录均在短时间内出现明显的上调表达,说明FcDorsal对鳗弧菌非常敏感。 作为核转录因子的NF-κB蛋白的转录激活作用需要在细胞质中通过蛋白水解作用来激活,为了进一步阐明NF-κB对病菌感染的应答机制,需要进一步研究这两种转录因子在蛋白水平的变化,以便从分子水平阐明NF-κB在对虾天然免疫中的作用。

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本文以鲜活饵料赤子爱胜蚓(Eisenia foetida)为研究对象,从营养学和免疫学的角度研究探讨了蚯蚓对对虾生长和抗病力的影响,为目前虾病问题的解决进行了有益的探索,为蚯蚓在规模化养殖生产中的推广应用提供了参考和依据。主要研究结果如下: 1、以鲜活饵料赤子爱胜蚓为主,双齿围沙蚕(Perinereis aibuhitensis)和人工配合饵料为对照,比较研究了凡纳滨对虾(Litopenaeus vannamei)摄食不同饵料的生长和免疫指标的差异。结果表明:沙蚕和蚯蚓单独投喂或与人工饵料配合投喂都可显著提高凡纳滨对虾的生长速率,提高对虾肌肉蛋白的营养价值,但用沙蚕单独投喂的对虾成活率较低。在增强对虾的免疫功能方面,蚯蚓和沙蚕与人工饵料配合投喂优于蚯蚓和沙蚕单独投喂,同时蚯蚓的饵料效果优于沙蚕。 2、采用鲜活饵料赤子爱胜蚓和人工配合饵料的不同配比投喂处于健康状态下的中国明对虾(Fenneropenaeus chinensis)幼虾,研究了其生长和免疫特征。结果表明:在人工饵料中配合投喂1/4的蚯蚓(干重)可显著加快中国明对虾的生长速率,增加对虾肌肉蛋白质含量,提高对虾肌肉蛋白的营养价值,减少脂肪含量,但对处于健康状态下的中国明对虾幼虾免疫功能的增强无明显效果。 3、考虑到对虾规模化养殖的可行性,采用冰冻蚯蚓赤子爱胜蚓和人工饵料的不同配比投喂处于非健康状态下的凡纳滨对虾,测定分析对虾的生长、营养成分和免疫指标,结果表明:蚯蚓投喂量(干重)占日投喂量的1/4时可以显著提高对虾的生长速率,增加对虾营养,增强对虾免疫功能,提高对虾成活率。 我国蚯蚓资源丰富,来源广泛,研究证实,以蚯蚓作为对虾饵料可增加对虾营养,促进对虾生长,提高机体免疫力,是对虾规模化养殖生产中的优质绿色动物性饵料。

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本研究以中国对虾为材料,以杂交育种和选择育种为目标,进行了系统的中国对虾杂交育种试验、生长性状遗传参数试验及其分子遗传连锁图谱的构建工作。结果表明以不同地理群体杂交作为基础群体,然后采用系统的选择育种方法可以获得较好的选择效果。构建的遗传连锁图谱为中国对虾分子辅助育种提供一定的基础。这些试验结果为中国对虾合理系统的育种工作提供了理论基础和数据支持。其具体结果如下: 1. 试验对中国对虾黄渤海水域乳山湾群体(WYP)和朝鲜半岛南海群体(WKN)的2个群体及其杂交后代不同月龄生长情况和存活率进行了研究,测量体长(TL)、头胸甲长(CL)、头胸甲宽(CW)、第2、3腹节高(HST)、第2、3腹节宽(WST)、体重(BW)和存活率共7个性状,计算各项指标的杂种优势率,并对各性状进行了方差分析和多重比较。其3月龄生长情况和存活率研究结果表明,存活率在乳山湾群体(WYP♀)× 朝鲜半岛南海群体(WKN♂)杂交后代出现杂种劣势外,其他指标都表现出不同程度的杂种优势(4.37%~23.96% )。除了存活率外,杂交后代生长性状均显著高于亲本,乳山湾群体(WYP♀)×朝鲜半岛南海群体(WKN♂)杂交后代高于朝鲜半岛南海群体(WKN♀)× 乳山湾群体(WYP♂)杂交后代,黄渤海水域乳山湾群体高于朝鲜半岛南海群体后代。为确定测量性状与中国对虾体重的相关程度,建立了用体长(X1),头胸甲宽(X2),第2、3腹节宽(X3),头胸甲长(X4),第2、3腹节高(X5)估计体重的多元回归方程:Y = -2.056 + 0.03X1 + 0.076X2 + 0.078X3 + 0.033X4 + 0.043X5。 2. 中国对虾黄渤海水域乳山湾群体(WYP)和朝鲜半岛南海群体(WKN)2个群体及其杂交后代在4月龄时期的6个生长指标和存活率的杂种优势范围在0.514%到14.95%之间,WYP♀×WKN♂杂交后代在这7个指标中都高于WKN♀×WYP♂杂交后代。5月龄杂交后代也表现出一定程度的杂种优势,其范围在-9.000%~19.090%之间,但头胸甲长、第2、3腹节处高和存活率3个指标出现杂种劣势。不同杂交组合各个阶段生长发育情况和存活率在杂种优势表现出一定的规律。随着月龄的增加,WKN♀×WYP♂杂交后代杂种优势率有所增加,而WYP♀×WKN♂杂交后代的却有所降低。ANOVA分析结果表明,杂交后代在存活率方面与双亲差异不显著。4月龄的分析结果发现杂交后代在WST和BW这2个指标上存在显著差异。LSD多重比较结果显示,WYP♀×WKN♂杂交后代在BW指标上与亲本存在显著差异,在WST指标方面与其他3个组合的后代差异显著。5月龄的数据分析结果发现,杂交后代除体重存在显著差异外,其他各项指标差异均不显著。LSD多重比较结果发现,WKN♀×WYP♂杂交后代体重与其亲本WKN存在显著差异。 3. 对2个野生群体——朝鲜半岛南海岸群体(WKN)和黄渤海群体(WYP)和3个养殖群体——朝鲜半岛群体的养殖一代(FKN),黄海1号(HH1)和即抗98(JK98)进行杂交试验的研究,结果表明JK98 (♀)  WKN (♂)组合在存活率方面最高,其余的依次为WYP (♀) WKN (♂),WKN (♀) WYP (♂),FKN (♀)HH1 (♂) 和 WYP (♀) FKN (♂)。而在体重方面FKN(♀)  HH1(♂)组合最高,其余的依次为WKN (♀) WYP (♂),WYP (♀) WKN (♂),WYP (♀)FKN (♂) 和 JK98 (♀)WKN (♂)。在所有生长性状方面,JK98 (♀)  WKN (♂)在5个组合中是最低的。方差检测结果表明,TL、CL、HST、LL和BW这5个指标在不同组合间存在差异,而其他指标不存在差异。多重比较结果发现JK98 (♀)WKN (♂)组合的TL与其他组合间差异极显著,HST指标与WKN (♀) WYP (♂),FKN(♀)  HH1(♂)和 WYP (♀)  WKN (♂)这3个组合差异显著,BW指标与WKN (♀) WYP (♂) 和 FKN(♀)  HH1(♂)差异显著。 4. 通过人工授精的方法建立了中国对虾21个半同胞家系,测量了中国对虾21个半同胞(46个全同胞)家系的TL、CL、CW、HST、WST、第1腹节长(FL)、第6腹节长(LL)。利用MTDFREML软件得到生长性状遗传力在0.15~0.35之间,属于中度遗传力范围。TL的遗传力为0.34±0.071,CL的为0.30±0.070,CW为0.35±0.077,WST为0.33±0.073,HST为0.33±0.073,FL的最低为0.15±0.044,LL的为0.24±0.059。各个性状间表现出高的正相关,其中CW和TL以及HST的遗传相关最大,FL和WST的遗传相关最小。 通过以上杂交育种和选择育种的研究,认为单纯的依靠杂交育种来改善中国对虾的育种工作可能具有一定的局限性。所以在实际的育种过程中,以中国对虾不同群体的杂交后代作为基础群体,并以此为基础进行系统的选择育种应该具有更大的潜力。 5. 本试验利用中国对虾F2群体和AFLP分子标记技术进行了遗传连锁图谱的构建。利用55对AFLP引物组合对F2家系的110个个体进行了研究,结果检测到532个符合作图策略的AFLP标记。利用卡方检验检测分离位点是否符合孟德尔分离定律。对于符合3:1比例的分离位点利用F2自交模型构建性别平均连锁图谱,对于符合1:1比例的分离位点利用拟测交理论分别构建中国对虾的雌性和雄性遗传连锁图谱。雌性、雄性和性别平均遗传图谱分别有28、35和44个连锁群,图谱实际长度分别为1090、1617和1772.1 cM。中国对虾遗传连锁图谱估计基因组长度为2420 cM,符合与人类基因组相比的对虾类基因组长度。中国对虾雄性遗传连锁图谱比雌性遗传连锁图谱长32.6%,这可能说明中国对虾不同性别存在不同的重组率。通过皮尔逊相关系数检测认为AFLP标记在中国对虾图谱上分布均匀。本文利用AFLP标记构建的中国对虾遗传连锁图谱为中国对虾基因组研究和遗传改良提供一定的基础,同时也应该开发微卫星等共显性标记,为遗传连锁图谱的整合提供条件。

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对虾病害在世界范围内肆虐,给水产养殖和沿海农村经济造成了重大损失。在水产养殖的实践中快速检测水产动物的病害并及时采取隔离等措施对于控制病害尤为重要,其中关键的环节就是快速检测出病害,并在对虾免疫机制上寻找对虾疾病防治的有效方法。研究表明当对虾等甲壳动物受到外界病原刺激时,极微量的微生物多糖就可以激活proPO系统。激活过程中涉及和产生一系列活性物质,如黑色素、酚氧化酶原激活因子(PPA)、模式识别蛋白(BGBP、PGBP、LGBP、LBP)及其膜上受体和A2巨球蛋白等,它们可通过多种方式参与防御反应,包括提供调理素,促进血细胞吞噬作用,形成结节或包囊以及介导凝集和凝固,产生杀菌物质并且黑色素化。黑色素常常在节肢动物的体表形成黑色斑点,形成的色素沉着对机体起到保护作用。所以,酚氧化酶原激活的级联反应是节肢动物免疫的关键因素。本论文研究开发了以环等温介导技术(LAMP)为基础的检测对虾白斑病毒(WSSV)和鳗弧菌(V. anguillarum)的快速检测方法。并从对虾对病害的免疫机制为切入点,从中国明对虾体内克隆了酚氧化酶原(PrpPO)和丝氨酸蛋白酶FcSP3这两个免疫系统中重要的基因,分析了它们的分子结构特征,组织分布及应答鳗弧菌病原刺激的表达变化模式。 建立的对虾常见病害对虾白班病毒(WSSV)和鳗弧菌(V. anguillarum)的LAMP检测方法,经过实验比对和Blast检索,发现本研究中使用的引物,比已经报导的LAMP方法或者PCR方法具有更宽的检测范围(更低的假阴性)。检测WSSV的LAMP方法使用病毒的VP28基因设计引物,而鳗弧菌的检测方法使用empA基因设计引物。在方法中,首次提出加入UNG酶和dUTP的措施来预防污染,在实际检测中非常有效。LAMP方法与PCR检测方法的灵敏性比较也进行了研究,二者灵敏性相当。 依据中国明对虾血液cDNA文库提供的部分片段信息,结合SMART-RACE技术,克隆了酚氧化酶原(PrpPO)基因,通过序列比对分析发现,PrpPO基因cDNA全长为3040 bp,其中开放阅读框2061 bp,编码686个氨基酸,其中推测的信号肽为12个氨基酸。推测的序列与斑节对虾(P. monodon)同源性为93%,与短钩对虾(P. semisulcatus.)同源性为92%。real time RT-PCR实验结果表明, ProPO在血细胞中的相对表达量最高,肝胰脏中表达量最低。弧菌刺激实验中注射弧菌,刺激了血细胞和淋巴器官中的ProPO mRNA显著增加,说明在血细胞和淋巴器官中存在快速反应的ProPO通路。而ProPO mRNA量在淋巴器官中在时间上早于血液中升至最高,说明该动物在在病原刚开始入侵的时候先有淋巴器官发挥主要的免疫作用,随着时间推移血细胞便变成主要的免疫器官。 根据中国明对虾肝胰脏cDNA文库提供EST信息,经过SMART-RACE克隆了一个丝氨酸蛋白酶FcSP3基因,通过序列比对分析发现,该丝氨酸蛋白酶基因cDNA全长为1622 bp,其中开放阅读框1431 bp,编码477个氨基酸,其中推测的信号肽为22个氨基酸。推测的序列与疟蚊的丝氨酸蛋白酶(A. gambiae)同源性为33%,与丽蝇蛹集金小蜂的酚氧化酶原激活因子(N. vitripennis)同源性为32%,与东北大黑鳃金龟的酚氧化酶原激活因子(H. diomphalia)同源性为34%。淋巴器官中PPAⅡ表达量约为血液中表达量的47560倍,肝胰脏中的FCSP3表达量为血细胞表达量的6226倍。鳗弧菌注射对虾后,淋巴器官中刺激组和对照组FcSP3的mRNA量在刺激后6小时显著降低,但是刺激组的表达量明显高于对照组。刺激组的血细胞与肝胰脏中FcSP3 mRNA的相对表达量增高。而病原刺激后的血液与肝胰脏中的FcSP3 mRNA的增长趋势也在时间上先与ProPO mRNA。这说明FcSP3对ProPO有正调控的作用,但这个调控有一个时间差,并且在不同组织中有不同的调控效率。