Dhar Bishal, Ghosh Sankar Kumar
Department of Biotechnology, Assam University, Silchar 788011, Assam, India.
Department of Biotechnology, Assam University, Silchar 788011, Assam, India; University of Kalyani, Kalyani 741235, West Bengal, India.
Gene. 2017 Sep 5;627:248-254. doi: 10.1016/j.gene.2017.06.043. Epub 2017 Jun 23.
The ornamental fishes were exported under the trade names or generic names, thus creating problems in species identification. In this regard, DNA barcoding could effectively elucidate the actual species status. However, the problem arises if the specimen is having taxonomic disputes, falsified by trade/generic names, etc., On the other hand, barcoding the archival museum specimens would be of greater benefit to address such issues as it would create firm, error-free reference database for rapid identification of any species. This can be achieved only by generating short sequences as DNA from chemically preserved are mostly degraded. Here we aimed to identify a short stretch of informative sites within the full-length barcode segment, capable of delineating diverse group of ornamental fish species, commonly traded from NE India. We analyzed 287 full-length barcode sequences from the major fish orders and compared the interspecific K2P distance with nucleotide substitutions patterns and found a strong correlation of interspecies distance with transversions (0.95, p<0.001). We, therefore, proposed a short stretch of 171bp (transversion rich) segment as mini-barcode. The proposed segment was compared with the full-length barcodes and found to delineate the species effectively. Successful PCR amplification and sequencing of the 171bp segment using designed primers for different orders validated it as mini-barcodes for ornamental fishes. Thus, our findings would be helpful in strengthening the global database with the sequence of archived fish species as well as an effective identification tool of the traded ornamental fish species, as a less time consuming, cost effective field-based application.
观赏鱼以商品名或通用名出口,这给物种鉴定带来了问题。在这方面,DNA条形码技术可以有效地阐明实际的物种状况。然而,如果标本存在分类学争议、被商品名/通用名等伪造,问题就会出现。另一方面,对博物馆存档标本进行条形码编码将更有助于解决此类问题,因为它将创建一个可靠、无错误的参考数据库,以便快速鉴定任何物种。这只有通过生成短序列才能实现,因为化学保存的DNA大多已降解。我们的目标是在全长条形码片段中识别一段短的信息位点,能够区分从印度东北部常见交易的各种观赏鱼物种。我们分析了来自主要鱼类目287条全长条形码序列,并将种间K2P距离与核苷酸替换模式进行比较,发现种间距离与颠换有很强的相关性(0.95,p<0.001)。因此,我们提出了一段171bp(富含颠换)的短片段作为微型条形码。将该片段与全长条形码进行比较,发现它能有效地区分物种。使用针对不同目的设计引物对171bp片段进行成功的PCR扩增和测序,验证了它作为观赏鱼微型条形码的有效性。因此,我们的研究结果将有助于通过存档鱼类物种的序列加强全球数据库,并作为一种耗时少、成本效益高的基于现场的应用,成为交易观赏鱼物种的有效鉴定工具。