Velasco-Cuervo Sandra M, Aguirre-Ramirez Elkin, Gallo-Franco Jenny Johana, González Obando Ranulfo, Carrejo Nancy, Toro-Perea Nelson
Departamento de Biología, Sección de Genética, Universidad del Valle, Calle 13 # 100-00, Cali, Colombia.
Departamento de Biología, Sección de Entomología, Universidad del Valle, Calle 13 # 100-00, Cali, Colombia.
J Adv Res. 2018 Nov 23;16:123-134. doi: 10.1016/j.jare.2018.11.001. eCollection 2019 Mar.
The fragmentation of DNA in historical specimens is very common, so obtaining sequences that allow molecular identification and the study of diversity is quite challenging. In this study, we used preserved and fresh specimens of the fruit fly genus , a genus of economic impact of fruit crops of the Neotropic. From these specimens, we evaluated: (1) the success PCR amplification rates of mini-barcodes fragments of the subunit I (COI) gene, and (2) the usefulness of mini-barcodes in the reconstruction of haplotypes for the identification of species and the diversity analysis. We used 93 specimens from 12 species, which had been preserved in 70% ethanol for more than 20 years. Internal primers were designed in the COI region and primers available in the literature were also evaluated. We obtained amplifications for 62.36% of the samples processed, and reconstructed haplotypes between 171 bp and 632 bp. Variable amplification rates between combinations of primers and between species were obtained, and molecular identification of some museum specimens was achieved. It was also possible to compare the haplotypes obtained in four species from which both fresh and museum samples were available. Our results also show the importance of the adjustment of the primers for the amplification, allowing to amplify fragments of up to 400 bp. The use available resources in biological collections is key to increasing knowledge of species of interest, and by means of the amplification of mini-barcodes, short sequences can be obtained that allow the molecular identification of specimens and the reconstruction of haplotypes with multiple purposes.
历史标本中的DNA片段化非常普遍,因此获得能够进行分子鉴定和多样性研究的序列颇具挑战性。在本研究中,我们使用了果蝇属的保存标本和新鲜标本,果蝇属对新热带区的水果作物具有经济影响。从这些标本中,我们评估了:(1)细胞色素氧化酶亚基I(COI)基因的微型条形码片段的PCR扩增成功率,以及(2)微型条形码在重建单倍型以进行物种鉴定和多样性分析中的有用性。我们使用了来自12个物种的93个标本,这些标本已在70%乙醇中保存了20多年。在COI区域设计了内部引物,并对文献中可用的引物也进行了评估。我们对62.36%的处理样本进行了扩增,并重建了171 bp至632 bp之间的单倍型。获得了引物组合之间以及物种之间不同的扩增率,并实现了对一些博物馆标本的分子鉴定。还可以比较从新鲜样本和博物馆样本均有的四个物种中获得的单倍型。我们的结果还表明了调整引物进行扩增的重要性,从而能够扩增出长达400 bp的片段。利用生物标本馆中的现有资源是增加对感兴趣物种了解的关键,通过微型条形码的扩增,可以获得短序列,从而实现标本的分子鉴定和多种用途的单倍型重建。