开发用于快速鉴定多种 Saccostrea 物种的多重 PCR 检测方法,并将其实际应用于修复和水产养殖。

IF 2.3 Q2 ECOLOGY BMC ecology and evolution Pub Date : 2024-05-21 DOI:10.1186/s12862-024-02250-1
Marina A Richardson, Nikolina Nenadic, Max Wingfield, Carmel McDougall
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摘要

背景:人们对热带地区牡蛎(蚝科)的生态学和生物学知之甚少。牡蛎的形态可塑性和共同特征导致了物种的错误识别,给了解物种特异性的基本生物信息带来了挑战,而这些信息是恢复和水产养殖所必需的。事实证明,遗传条形码对准确识别物种和了解物种地理范围至关重要。为了降低分子物种鉴定的成本,我们利用细胞色素 c 氧化酶亚单位 I(COI 或 cox1)条形码基因开发了多重检测方法,用于快速鉴定澳大利亚昆士兰州常见的 Saccostrea 属中的五个牡蛎物种:结果显示:多重检测成功地鉴定了澳大利亚昆士兰常见的 Saccostrea 属中的五个牡蛎物种:Saccostrea glomerata、Saccostrea B 系、Saccostrea F 系、Saccostrea G 系和 Saccostrea spathulata(J 系):多重检测成功地对目标物种进行了物种特异性扩增。这些引物的实际应用在昆士兰莫尔顿湾一个试点恢复项目中收集的野生蛎壳上进行了测试,通过桑格测序验证了已确定的物种(S. glomerata、B 系和 G 系)。此外,还对从昆士兰州努萨河口采集的成年牡蛎进行了提取牡蛎表皮液的 DNA 取样测试,以评估是否能以非破坏性方式识别牡蛎。在大多数情况下,低至 1 纳克/微升的 DNA 浓度仍可扩增,从而进行鉴定,而且在采集牡蛎鳞片液 6 周后的死亡率很低(104 只采样牡蛎中只有 3 只死亡):这些多重检测方法将成为未来研究中物种鉴定的重要工具,我们成功地展示了它们在昆士兰修复和水产养殖中的实际应用。本研究中开发的多重检测方法很容易复制,可用于开发更多物种特异性引物集,以快速鉴定在印度洋-太平洋地区发现的 Saccostrea 其他物种,这将有助于解开热带地区该属物种分类的模糊性。
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The development of multiplex PCR assays for the rapid identification of multiple Saccostrea species, and their practical applications in restoration and aquaculture.

Background: The ecology and biology of oysters (Ostreidae) across the tropics is poorly understood. Morphological plasticity and shared characteristics among oysters have resulted in the misidentification of species, creating challenges for understanding basic species-specific biological information that is required for restoration and aquaculture. Genetic barcoding has proven essential for accurate species identification and understanding species geographic ranges. To reduce the costs of molecular species identification we developed multiplex assays using the cytochrome c oxidase subunit I (COI or cox1) barcoding gene for the rapid identification of five species of oysters within the genus Saccostrea that are commonly found in Queensland, Australia: Saccostrea glomerata, Saccostrea lineage B, Saccostrea lineage F, Saccostrea lineage G, and Saccostrea spathulata (lineage J).

Results: Multiplex assays were successful in species-specific amplification of targeted species. The practical application of these primers was tested on wild spat collected from a pilot restoration project in Moreton Bay, Queensland, with identified species (S. glomerata, lineage B and lineage G) validated by Sanger sequencing. DNA sampling by extraction of oyster pallial fluid was also tested on adult oysters collected from the Noosa estuary in Queensland to assess whether oysters were able to be identified non-destructively. DNA concentrations as low as 1 ng/ μL still amplified in most cases, allowing for identification, and mortality at 6 weeks post pallial fluid collection was low (3 out of 104 sampled oysters).

Conclusion: These multiplex assays will be essential tools for species identification in future studies, and we successfully demonstrate their practical application in both restoration and aquaculture contexts in Queensland. The multiplex assays developed in this study outline easily replicable methods for the development of additional species-specific primer sets for the rapid identification of other species of Saccostrea found across the Indo-Pacific, which will be instrumental in unravelling the taxonomic ambiguities within this genus in tropical regions.

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