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Genetic resources in wild and cultured stocks of the Asian mud crab, Scylla paramamosain

机译:亚洲泥蟹Sylla paramamosain野生和养殖种群的遗传资源

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摘要

The mud crab (Scylla spp.) aquaculture industry has expanded rapidly in recent years in many countries in the Indo - West Pacific (IWP) region as an alternative to marine shrimp culture because of significant disease outbreaks and associated failures of many shrimp culture industries in the region. Currently, practices used to produce and manage breeding crabs in hatcheries may compromise levels of genetic diversity, ultimately compromising growth rates, disease resistance and stock productivity. Therefore, to avoid “genetic pollution” and its harmful effects and to promote further development of mud crab aquaculture and fisheries in a sustainable way, a greater understanding of the genetic attributes of wild and cultured mud crab stocks is required. Application of these results can provide benefits for managing wild and cultured Asian mud crab populations for multiple purposes including for commercial production, recreation and conservation and to increase profitability and sustainability of newly emerging crab culture industries. Phylogeographic patterns and the genetic structure of Asian mud crab populations across the IWP were assessed to determine if they were concordant with those of other widespread taxa possessing pelagic larvae of relatively long duration. A 597 bp fragment of the mitochondrial DNA COI gene was amplified and screened for variation in a total of 297 individuals of S. paramamosain from six sampling sites across the species’ natural geographical distribution in the IWP and 36 unique haplotypes were identified. Haplotype diversities per site ranged from 0.516 to 0.879. Nucleotide diversity estimates among haplotypes were 0.11% – 0.48%. Maximum divergence observed among S. paramamosain samples was 1.533% and samples formed essentially a single monophyletic group as no obvious clades were related to geographical location of sites. A weak positive relationship was observed however, between genetic distance and geographical distance among sites. Microsatellite markers were then used to assess contemporary gene flow and population structure in Asian mud crab populations sampled across their natural distribution in the IWP. Eight microsatellite loci were screened in sampled S. paramamosain populations and all showed high allelic diversity at all loci in sampled populations. In total, 344 individuals were analysed, and 304 microsatellite alleles were found across the 8 loci. The mean number of alleles per locus at each site ranged from 20.75 to 28.25. Mean allelic richness per site varied from 17.2 to 18.9. All sites showed high levels of heterozygosity as average expected heterozygosities for all loci ranged from 0.917 – 0.953 while mean observed heterozygosity ranged from 0.916 – 0.959. Allele diversities were similar at all sites and across all loci. The results did not show any evidence for major differences in allele frequencies among sites and patterns of allele frequencies were very similar in all populations across all loci. Estimates of population differentiation (FST) were relatively low and most probably largely reflect intra – individual variation for very highly variable loci. Results from nDNA analysis showed evidence for only very limited population genetic structure among sampled S. paramamosain, and a positive and significant association for genetic and geographical distance among sample sites. Microsatellite markers were then employed to determine if adequate levels of genetic diversity has been captured in crab hatcheries for the breeding cycle. The results showed that all microsatellite loci were polymorphic in hatchery samples. Culture populations were in general, highly genetically depauperate, compared with comparable wild populations, with only 3 to 8 alleles recorded for the same loci set per population. In contrast, very high numbers of alleles per locus were found in reference wild S. paramamosain populations, which ranged from 18 to 46 alleles per locus per population. In general, this translates into a 3 to 10 fold decline in mean allelic richness per locus in all culture stocks compared with wild reference counterparts. Furthermore, most loci in all cultured S. paramamosain samples showed departures from HWE equilibrium. Allele frequencies were very different in culture samples from that present in comparable wild reference samples and this in particular, was reflected in a large decline in allele diversity per locus. The pattern observed was best explained by significant impacts of breeding practices employed in hatcheries rather than natural differentiation among wild populations used as the source of brood stock. Recognition of current problems and management strategies for the species both for the medium and long-term development of the new culture industry are discussed. The priority research to be undertaken over the medium term for S. paramamosain should be to close the life cycle fully to allow individuals to be bred on demand and their offspring equalised to control broodstock reproductive contributions. Establishing a broodstock register and pedigree mating system will be required before any selection program is implemented. This will ensure that sufficient genetic variation will be available to allow genetic gains to be sustainably achieved in a future stock improvement program. A fundamental starting point to improve hatchery practices will be to encourage farmers and hatchery managers to spawn more females in their hatcheries as it will increase background genetic diversity in culture stocks. Combining crablet cohorts from multiple hatcheries into a single cohort for supply to farmers or rotation of breeding females regularly in hatcheries will help to address immediate genetic diversity problems in culture stocks. Application of these results can provide benefits for managing wild and cultured Asian mud crab populations more efficiently. Over the long-term, application of data on genetic diversity in wild and cultured stocks of Asian mud crab will contribute to development of sustainable and productive culture industries in Vietnam and other countries in the IWP and can contribute towards conservation of wild genetic resources.
机译:近年来,由于西印度洋-西太平洋(IWP)地区许多疾病的爆发和许多虾类养殖业的相关失败,泥蟹(Scylla spp。)的养殖业在印度洋-西太平洋(IWP)地区的许多国家迅速发展。该区域。当前,用于在孵化场生产和管理繁殖蟹的做法可能会损害遗传多样性的水平,最终损害增长率,抗病性和种群生产力。因此,为了避免“遗传污染”及其有害影响,并以可持续的方式促进泥蟹水产养殖和渔业的进一步发展,需要对野生和养殖泥蟹种群的遗传特性有更多的了解。这些结果的应用可以为管理野生和养殖亚洲泥蟹种群提供多种益处,包括用于商业生产,娱乐和保护等多种用途,并增加新兴蟹养殖业的盈利能力和可持续性。评估了整个IWP中亚洲泥蟹种群的系统记录模式和遗传结构,以确定它们是否与其他具有相对较长持续时间的中上层幼虫的其他广泛分类单元一致。扩增并筛选了线粒体DNA COI基因的597 bp片段,从IWP中该物种自然地理分布的六个采样点中的共297个副嗜毛链球菌个体进行了变异,并鉴定出36种独特的单倍型。每个位点的单倍型多样性为0.516至0.879。单倍型之间的核苷酸多样性估计为0.11%– 0.48%。在S. paramamosain样品之间观察到的最大差异为1.533%,并且样品基本上形成一个单一的系统组,因为没有明显的进化枝与位点的地理位置有关。然而,在站点之间的遗传距离和地理距离之间观察到了弱的正相关。然后,微卫星标记被用于评估在IWP中通过其自然分布取样的亚洲泥蟹种群的当代基因流和种群结构。在抽样的副嗜杀链球菌种群中筛选了八个微卫星基因座,并且在抽样种群的所有基因座上均显示出高等位基因多样性。总共分析了344个个体,在8个基因座中发现了304个微卫星等位基因。每个位点在每个位点的平均等位基因数范围为20.75至28.25。每个位点的平均等位基因丰富度从17.2至18.9不等。所有位点均显示高杂合度,所有基因座的平均预期杂合度在0.917 – 0.953之间,而平均观察到的杂合度在0.916 – 0.959之间。所有位点和所有基因座的等位基因多样性都相似。结果没有显示任何证据表明位点之间的等位基因频率存在重大差异,并且在所有位点的所有人群中等位基因频率的模式都非常相似。种群分化(FST)的估计值相对较低,很可能很大程度上反映了高度可变位点的个体内部差异。 nDNA分析的结果表明,证据仅显示抽样的副嗜杀沙门氏菌中的种群遗传结构非常有限,并且样本位点之间的遗传和地理距离呈正相关关系。然后,使用微卫星标记确定蟹孵化场是否已为繁殖周期捕获到​​足够水平的遗传多样性。结果表明,孵化场样本中的所有微卫星基因座都是多态的。与可比的野生种群相比,培养种群总体上遗传上无繁殖力,每个种群的相同基因座集仅记录了3至8个等位基因。相比之下,在参照野生嗜酸链球菌参考野生种群中,每个基因座的等位基因数量很高,每个种群每个基因座的等位基因范围为18至46个等位基因。通常,与野生参考对应物相比,这意味着所有培养物中每个基因座的平均等位基因丰富度下降了3到10倍。此外,在所有培养的副嗜乳链球菌样品中的大多数基因座均显示出偏离HWE平衡。培养样品中的等位基因频率与可比较的野生参考样品中的等位基因频率有很大不同,尤其是,反映在每个基因座的等位基因多样性大大下降。孵化场采用的育种方法的重大影响,而不是用作亲鱼来源的野生种群之间的自然分化,可以最好地解释观察到的模式。讨论了新文化产业的中长期发展对物种当前问题的认识和管理策略。在中期,将对副寄生沙门氏菌进行的优先研究应是完全关闭生命周期,以便按需繁殖个体,使其后代均衡以控制亲鱼的繁殖贡献。在实施任何选拔程序之前,都需要建立亲虾登记册和家谱交配系统。这将确保有足够的遗传变异,以便在未来的种群改良计划中可持续实现遗传增益。改善孵化场实践的根本出发点将是鼓励农民和孵化场管理者在其孵化场中产卵更多的雌性,因为这将增加养殖种群的背景遗传多样性。将来自多个孵化场的螃蟹群合并为一个单一群,以提供给农民或在孵化场定期轮换育种雌性,将有助于解决养殖种群中的直接遗传多样性问题。这些结果的应用可以为更有效地管理亚洲野生和养殖泥蟹种群提供好处。长期而言,将亚洲泥蟹野生和养殖种群遗传多样性数据的应用将有助于在IWP中发展越南和其他国家的可持续和生产性养殖产业,并有助于保护野生遗传资源。

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    Le Van Chi;

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  • 年度 2010
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