Speller Camilla F, Nicholas George P, Yang Dongya Y
Centre for Forensic Research, Ancient DNA Laboratory, Department of Archaeology, Simon Fraser University, 8888 University Drive, Burnaby, BC, V5A 1S6, Canada.
Investig Genet. 2011 Jul 28;2:16. doi: 10.1186/2041-2223-2-16.
The ability to accurately identify bird species is crucial for wildlife law enforcement and bird-strike investigations. However, such identifications may be challenging when only partial or damaged feathers are available for analysis.
By applying vigorous contamination controls and sensitive PCR amplification protocols, we found that it was feasible to obtain accurate mitochondrial (mt)DNA-based species identification with as few as two feather barbs. This minimally destructive DNA approach was successfully used and tested on a variety of bird species, including North American wild turkey (Meleagris gallopavo), Canada goose (Branta canadensis), blue heron (Ardea herodias) and pygmy owl (Glaucidium californicum). The mtDNA was successfully obtained from 'fresh' feathers, historic museum specimens and archaeological samples, demonstrating the sensitivity and versatility of this technique.
By applying appropriate contamination controls, sufficient quantities of mtDNA can be reliably recovered and analyzed from feather barbs. This previously overlooked substrate provides new opportunities for accurate DNA species identification when minimal feather samples are available for forensic analysis.
准确识别鸟类物种的能力对于野生动物执法和鸟类撞击事件调查至关重要。然而,当仅有部分或受损羽毛可供分析时,此类识别可能具有挑战性。
通过实施严格的污染控制和灵敏的聚合酶链反应(PCR)扩增方案,我们发现用少至两根羽支获得基于线粒体(mt)DNA的准确物种识别是可行的。这种微创性的DNA方法已成功应用于多种鸟类并进行了测试,包括北美野火鸡(Meleagris gallopavo)、加拿大鹅(Branta canadensis)、苍鹭(Ardea herodias)和侏鸺(Glaucidium californicum)。线粒体DNA已成功从“新鲜”羽毛、历史博物馆标本和考古样本中获得,证明了该技术的灵敏性和通用性。
通过实施适当的污染控制,可从羽支可靠地回收和分析足够量的线粒体DNA。当仅有极少羽毛样本可用于法医分析时,这种先前被忽视的样本为准确的DNA物种识别提供了新机会。