Noninvasive population assessment of moose (Alces alces) by SNP genotyping of fecal pellets

Abstract Noninvasive genetic studies of wild animals enable the recovery of information infeasible to obtain using other means. However, the low quantity and quality of noninvasively collected DNA often challenge the retrieval of reliable genotypes, which may cause biases in downstream analyses. In...

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Bibliographic Details
Published in:European Journal of Wildlife Research
Main Authors: Blåhed, Ida-Maria, Ericsson, Göran, Spong, Göran
Other Authors: Sveriges Lantbruksuniversitet, Statens veterinärmedicinska anstalt, Svenska Jägareförbundet, Lennanders stipendiestiftelse
Format: Article in Journal/Newspaper
Language:English
Published: Springer Science and Business Media LLC 2019
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Online Access:http://dx.doi.org/10.1007/s10344-019-1337-8
http://link.springer.com/content/pdf/10.1007/s10344-019-1337-8.pdf
http://link.springer.com/article/10.1007/s10344-019-1337-8/fulltext.html
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Summary:Abstract Noninvasive genetic studies of wild animals enable the recovery of information infeasible to obtain using other means. However, the low quantity and quality of noninvasively collected DNA often challenge the retrieval of reliable genotypes, which may cause biases in downstream analyses. In this study, we optimized SNP (single nucleotide polymorphism) genotyping of fecal samples from moose ( Alces alces ) with the main purpose of exploring the potential of using noninvasively retrieved genotypes for individual- and sex identification. Fecal pellets were collected during the late winter of 2016 on the Swedish island of Öland in the Baltic Sea and DNA was extracted and genotyped using 86 autosomal, six sex-specific and five species diagnostic SNPs. The SNP error rate of the quality filtered dataset was 0.06 and the probability of identity for siblings below 0.001. Following a thorough quality filtering process, 182 reliable genotypes were obtained, corresponding to 100 unique individuals (37 males, 63 females), with an estimated male proportion of 37% (± 9%). The population size, estimated using two different capture-mark-recapture approaches, was found to be in the range of 115–156 individuals (95% CI). Furthermore, moose on Öland showed significantly lower heterozygosity levels (z Hexp = −5.51, N = 69, p Hexp = 3.56·10 −8 , z Hobs = −3.58, N = 69, p Hobs = 3.38·10 −4 ) and appeared genetically differentiated from moose on the Swedish mainland. Thus, we show that quality controlled noninvasively derived SNP genotypes can be highly informative for individual and population monitoring in a large ungulate.