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新鲜为佳:从考拉粪便中进行准确的单核苷酸多态性基因分型。

Fresh is best: Accurate SNP genotyping from koala scats.

作者信息

Schultz Anthony J, Cristescu Romane H, Littleford-Colquhoun Bethan L, Jaccoud Damian, Frère Céline H

机构信息

GeneCology Research Centre University of the Sunshine Coast Maroochydore DC Qld Australia.

Global Change Ecology Research Centre University of the Sunshine Coast Maroochydore DC Qld Australia.

出版信息

Ecol Evol. 2018 Feb 18;8(6):3139-3151. doi: 10.1002/ece3.3765. eCollection 2018 Mar.

DOI:10.1002/ece3.3765
PMID:29607013
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5869377/
Abstract

Maintaining genetic diversity is a crucial component in conserving threatened species. For the iconic Australian koala, there is little genetic information on wild populations that is not either skewed by biased sampling methods (e.g., sampling effort skewed toward urban areas) or of limited usefulness due to low numbers of microsatellites used. The ability to genotype DNA extracted from koala scats using next-generation sequencing technology will not only help resolve location sample bias but also improve the accuracy and scope of genetic analyses (e.g., neutral vs. adaptive genetic diversity, inbreeding, and effective population size). Here, we present the successful SNP genotyping (1272 SNP loci) of koala DNA extracted from scat, using a proprietary DArTseq protocol. We compare genotype results from two-day-old scat DNA and 14-day-old scat DNA to a blood DNA template, to test accuracy of scat genotyping. We find that DNA from fresher scat results in fewer loci with missing information than DNA from older scat; however, 14-day-old scat can still provide useful genetic information, depending on the research question. We also find that a subset of 209 conserved loci can accurately identify individual koalas, even from older scat samples. In addition, we find that DNA sequences identified from scat samples through the DArTseq process can provide genetic identification of koala diet species, bacterial and viral pathogens, and parasitic organisms.

摘要

维持遗传多样性是保护濒危物种的关键组成部分。对于标志性的澳大利亚考拉而言,关于野生种群的遗传信息极少,不是因有偏差的采样方法(例如,采样工作偏向城市地区)而产生偏差,就是由于所使用的微卫星数量少而实用性有限。利用下一代测序技术对从考拉粪便中提取的DNA进行基因分型,不仅有助于解决位置样本偏差问题,还能提高遗传分析的准确性和范围(例如,中性与适应性遗传多样性、近亲繁殖以及有效种群大小)。在此,我们展示了使用专有的DArTseq方案对从粪便中提取的考拉DNA成功进行单核苷酸多态性基因分型(1272个单核苷酸多态性位点)。我们将两天大的粪便DNA和14天大的粪便DNA的基因分型结果与血液DNA模板进行比较,以测试粪便基因分型的准确性。我们发现,较新鲜粪便中的DNA相比陈旧粪便中的DNA,信息缺失的位点更少;然而,根据研究问题的不同,14天大的粪便仍能提供有用的遗传信息。我们还发现,一个由209个保守位点组成的子集甚至可以从陈旧的粪便样本中准确识别出个体考拉。此外,我们发现通过DArTseq过程从粪便样本中鉴定出的DNA序列可以对考拉的食物种类、细菌和病毒病原体以及寄生生物进行遗传鉴定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f154/5869377/a7d2556e9821/ECE3-8-3139-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f154/5869377/77d6973d0ad9/ECE3-8-3139-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f154/5869377/732a9b5aeb15/ECE3-8-3139-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f154/5869377/a7d2556e9821/ECE3-8-3139-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f154/5869377/77d6973d0ad9/ECE3-8-3139-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f154/5869377/732a9b5aeb15/ECE3-8-3139-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f154/5869377/a7d2556e9821/ECE3-8-3139-g003.jpg

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