Quality of DNA extracted from freshwater fish scales and mucus and its application in genetic diversity studies of Perca fluviatilis and Rutilus rutilus.

IF 2.5 Q3 BIOCHEMICAL RESEARCH METHODS Biology Methods and Protocols Pub Date : 2023-09-28 eCollection Date: 2023-01-01 DOI:10.1093/biomethods/bpad022
Ieva Ignatavičienė, Adomas Ragauskas, Vytautas Rakauskas, Dalius Butkauskas
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Abstract

Studies on genetic diversity require biological material containing a reliable source of DNA that can be extracted and analyzed. Recently, non-invasive sampling has become a preferred sampling method of biological material. The suitability of a less invasive approach that involves obtaining samples by swabbing the fish skin (including live, non-anesthetized fish) should be considered. In this study, we compared the efficiency of DNA extraction, amplification, and sequencing of mtDNA fragments of two fish species Perca fluviatilis and Rutilus rutilus based on DNA collected from the scales and mucus using the modified Aljanabi and Martinez method. The results revealed a higher quality of DNA extracted from the mucus; however, the mean DNA concentration obtained from the scales of both fish species was higher. We verified the method suitable for amplification and sequencing of mtDNA fragments of both fish species using newly designed markers (D-loop, ATP6) and examined the potential risk of intraspecific cross-contamination. The DNA sequence alignment analysis revealed identical sequences attributed to the same individual when DNA, extracted from two different sources (scales and mucus), was used. We demonstrated that the quantity and quality of DNA extracted from the scales and mucus using the proposed method were high enough to carry out genetic diversity studies based on sampling of live fish with the possibility to release it after collecting samples.

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从淡水鱼鳞和粘液中提取的DNA质量及其在河豚和鲁蒂鲁遗传多样性研究中的应用。
对遗传多样性的研究需要含有可提取和分析的可靠DNA来源的生物材料。近年来,无创采样已成为生物材料的首选采样方法。应考虑通过擦拭鱼皮(包括活的、未麻醉的鱼)获取样本的微创方法的适用性。在本研究中,我们使用改良的Aljanabi和Martinez方法,基于从鳞片和粘液中收集的DNA,比较了两种鱼类Perca fluviatilis和Rutilus Rutilus mtDNA片段的DNA提取、扩增和测序效率。结果显示,从粘液中提取的DNA质量更高;然而,从两种鱼类的鳞片中获得的平均DNA浓度更高。我们使用新设计的标记物(D-loop,ATP6)验证了适用于扩增和测序两种鱼类mtDNA片段的方法,并检查了种内交叉污染的潜在风险。DNA序列比对分析显示,当使用从两种不同来源(鳞片和粘液)提取的DNA时,属于同一个体的相同序列。我们证明,使用所提出的方法从鳞片和粘液中提取的DNA的数量和质量足够高,可以在活鱼采样的基础上进行遗传多样性研究,并有可能在采集样本后释放。
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来源期刊
Biology Methods and Protocols
Biology Methods and Protocols Agricultural and Biological Sciences-Agricultural and Biological Sciences (all)
CiteScore
3.80
自引率
2.80%
发文量
28
审稿时长
19 weeks
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