Skip to main content
Log in

Obtaining high-quality DNA from elusive small mammals using low-tech hair snares

  • Original Paper
  • Published:
European Journal of Wildlife Research Aims and scope Submit manuscript

Abstract

Noninvasive sampling approaches are becoming increasingly important for enabling genetic studies of wildlife populations. While a number of methods have been described to noninvasively sample hair from carnivores and medium-sized mammals, they have largely remained untested in elusive small mammals. Here we describe a novel and inexpensive noninvasive hair snare targeted at an elusive small mammal, the American pika (Ochotona princeps). We explore the quality of the sample by assessing PCR amplification success of mitochondrial and nuclear DNA fragments across four commercially available DNA isolation kits and two different quantities of hair in a factorial design. Additionally, we determined the sex of the individual samples using PCR–RFLP of ZFX/ZFY loci. We found that our snare is effective in obtaining hair that yield DNA of sufficient quality and quantity to successfully amplify a range of mitochondrial and nuclear fragment sizes. Specifically, we found the greatest success in amplifying mitochondrial DNA, nuclear microsatellites and ZFX/ZFY loci using at least 25 hairs as starting material and the DNA IQ™ system. The hair snares thus provide a cost-effective and minimally intrusive approach to sample elusive or rare small mammals. We anticipate that this approach will be useful to obtain samples for molecular studies of the ecology, evolution and conservation of small, elusive mammals.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

References

  • Banks SC, Hoyle SD, Horsup A, Sunnucks P, Taylor AC (2003) Demographic monitoring of an entire species (the northern hairy-nosed wombat, Lasiorhinus krefftii) by genetic analysis of non-invasively collected material. Anim Conserv 6:101–107

    Article  Google Scholar 

  • Beever EA, Brussard PE, Berger J (2003) Patterns of apparent extirpation among isolated populations of pikas (Ochotona princeps) in the Great Basin. J Mammal 84:37–54

    Article  Google Scholar 

  • Beja-Pereira A, Oliveira R, Alves PC, Schwartz MK, Luikart G (2009) Advancing ecological understandings through technological transformations in noninvasive genetics. Mol Ecol Resour 9:1279–1301

    Article  PubMed  Google Scholar 

  • Bremner-Harrison S, Harrison SWR, Cypher BL, Murdoch JD, Maldonado J, Darden SK (2006) Development of a single-sampling noninvasive hair snare. Wildl Soc B 34:456–461

    Article  Google Scholar 

  • Broquet T, Petit E (2004) Quantifying genotyping errors in noninvasive population genetics. Mol Ecol 13:3601–3608

    Article  PubMed  CAS  Google Scholar 

  • Connior MB, Risch TS (2009) Live trap for pocket gophers. Southwest Nat 54:100–103

    Article  Google Scholar 

  • DeSalle R, Amato G (2004) The expansion of conservation genetics. Nat Rev Genet 5:702–712

    Article  PubMed  CAS  Google Scholar 

  • DeYoung RW, Honeycutt RL (2005) The molecular toolbox: genetic techniques in wildlife ecology and management. J Wildl Manage 69:1362–1384

    Article  Google Scholar 

  • Excoffier L, Heckel G (2006) Computer programs for population genetics data analysis: a survival guide. Nat Rev Genet 7:745–758

    Article  PubMed  CAS  Google Scholar 

  • Fontanesi L, Tazzoli M, Pecchioli E, Hauffe HC, Robinson TJ, Russo V (2008) Sexing European rabbits (Oryctolagus cuniculus), European brown hares (Lepus europaeus) and mountain hares (Lepus timidus) with ZFX and ZFY loci. Mol Ecol Resour 8:1294–1296

    Article  CAS  Google Scholar 

  • Gomez A, Wright PJ, Lunt DH, Cancino JM, Carvalho GR, Hughes RN (2007) Mating trials validate the use of DNA barcoding to reveal cryptic speciation of a marine bryozoan taxon. P R Soc B 274:199–207

    Article  CAS  Google Scholar 

  • Hedmark E, Flagstad O, Segerstrom P, Persson J, Landa A, Ellegren H (2004) DNA-based individual and sex identification from wolverine (Gulo gulo) faeces and urine. Conserv Genet 5:405–410

    Article  CAS  Google Scholar 

  • Henry P, Miquelle D, Sugimoto T, McCullough DR, Caccone A, Russello MA (2009) In situ population structure and ex situ representation of the endangered Amur tiger. Mol Ecol 18:3173–3184

    Article  PubMed  CAS  Google Scholar 

  • Kendall KC, Stetz JB, Boulanger J, Macleod AC, Paetkau D, White GC (2009) Demography and genetic structure of a recovering grizzly bear population. J Wildl Manage 73:3–17

    Article  Google Scholar 

  • Litvaitis JA, Tash JP, Litvaitis MK, Marchand MN, Kovach AI, Innes R (2006) A range-wide survey to determine the current distribution of New England cottontails. Wildl Soc B 34:1190–1197

    Article  Google Scholar 

  • Manchester KL (1995) Value of a(260)/a(280) ratios for measurement of purity of nucleic-acids. Biotechniques 19:208–210

    PubMed  CAS  Google Scholar 

  • Mitrovski P, Heinze DA, Guthridge K, Weeks AR (2005) Isolation and characterization of microsatellite loci from the Australian endemic mountain pygmy-possum, Burramys parvus Broom. Mol Ecol Notes 5:395–397

    Article  CAS  Google Scholar 

  • Morin PA, Chambers KE, Boesch C, Vigilant L (2001) Quantitative polymerase chain reaction analysis of DNA from noninvasive samples for accurate microsatellite genotyping of wild chimpanzees (Pan troglodytes verus). Mol Ecol 10:1835–1844

    Article  PubMed  CAS  Google Scholar 

  • Mullins J, Statham MJ, Roche T, Turner PD, O’Reilly C (2010) Remotely plucked hair genotyping: a reliable and non-invasive method for censusing pine marten (Martes martes, L. 1758) populations. Eur J Wildl Res 56:443–453

    Article  Google Scholar 

  • Mullis K, Faloona F, Scharf S, Saiki R, Horn H, Erlich H (1986) Specific enzymatic amplification of DNA in vitro: the polymerase chain reaction. Cold Spring Harb Symp Quant Biol 51:263

    PubMed  CAS  Google Scholar 

  • Nachman MW (2005) The genetic basis of adaptation: lessons from concealing coloration in pocket mice. Genetica 123:125–136

    Article  PubMed  CAS  Google Scholar 

  • Paetkau D (2003) An empirical exploration of data quality in DNA-based population inventories. Mol Ecol 12:1375–1387

    Article  PubMed  CAS  Google Scholar 

  • Pauli JN, Hamilton MB, Crain EB, Buskirk SW (2008) A single-sampling hair trap for mesocarnivores. J Wildl Manage 72:1650–1652

    Google Scholar 

  • Peacock MM (1997) Determining natal dispersal patterns in a population of North American pikas (Ochotona princeps) using direct mark-resight and indirect genetic methods. Behav Ecol 8:340–350

    Article  Google Scholar 

  • Peacock MM, Kirchoff VS, Merideth SJ (2002) Identification and characterization of nine polymorphic microsatellite loci in the North American pika, Ochotona princeps. Mol Ecol Notes 2:360–362

    Article  CAS  Google Scholar 

  • Piggott MP, Taylor AC (2003) Remote collection of animal DNA and its applications in conservation management and understanding the population biology of rare and cryptic species. Wildl Res 30:1–13

    Article  Google Scholar 

  • Piggott MP, Bellemain E, Taberlet P, Taylor AC (2004) A multiplex pre-amplification method that significantly improves microsatellite amplification and error rates for faecal DNA in limiting conditions. Conserv Genet 5:417–420

    Article  CAS  Google Scholar 

  • Regnaut S, Lucas FS, Fumagalli L (2006) DNA degradation in avian faecal samples and feasibility of non-invasive genetic studies of threatened capercaillie populations. Conserv Genet 7:449–453

    Article  CAS  Google Scholar 

  • Roon DA, Waits LP, Kendall KC (2003) A quantitative evaluation of two methods for preserving hair samples. Mol Ecol Notes 3:163–166

    Article  CAS  Google Scholar 

  • Roon DA, Waits LP, Kendall KC (2005) A simulation test of the effectiveness of several methods for error-checking non-invasive genetic data. Anim Conserv 8:203–215

    Article  Google Scholar 

  • Rudnick JA, Katzner TE, Bragin EA, DeWoody JA (2007) Species identification of birds through genetic analysis of naturally shed feathers. Mol Ecol Notes 7:757–762

    Article  CAS  Google Scholar 

  • Russello MA, Amato G (2001) Application of a noninvasive, PCR-Based test for sex identification in an endangered parrot, Amazona guildingii. Zoo Biol 20:41–45

    Article  PubMed  CAS  Google Scholar 

  • Russello MA, Glaberman S, Gibbs JP, Marquez C, Powell JR, Caccone A (2005) A cryptic taxon of Galapagos tortoise in conservation peril. Biol Lett-UK 1:287–290

    Article  Google Scholar 

  • Sastre N, Francino O, Lampreave G, Bologov VV, Lopez-Martin JM, Sanchez A, Ramirez O (2009) Sex identification of wolf (Canis lupus) using non-invasive samples. Conserv Genet 10:555–558

    Article  CAS  Google Scholar 

  • Smith AT, Weston ML (1990) Ochotona princeps. Mamm Species 352:1–8

    Article  Google Scholar 

  • Sunnucks P (2000) Efficient genetic markers for population biology. Trends Ecol Evol 15:199–203

    Article  PubMed  Google Scholar 

  • Taberlet P, Griffin S, Goossens B, Questiau S, Manceau V, Escaravage N, Waits LP, Bouvet J (1996) Reliable genotyping of samples with very low DNA quantities using PCR. Nucleic Acids Res 24:3189–3194

    Article  PubMed  CAS  Google Scholar 

  • Taberlet P, Waits LP, Luikart G (1999) Noninvasive genetic sampling: look before you leap. Trends Ecol Evol 14:323–327

    Article  PubMed  Google Scholar 

  • Toth M (2008) A new noninvasive method for detecting mammals from birds’ nests. J Wildl Manage 72:1237–1240

    Article  Google Scholar 

  • Waits LP, Paetkau D (2005) Noninvasive genetic sampling tools for wildlife biologists: a review of applications and recommendations for accurate data collection. J Wildl Manage 69:1419–1433

    Article  Google Scholar 

  • Willard JM, Lee DA, Holland MM (1998) Recovery of DNA for PCR amplification from blood and forensic samples using chelating resin. In: Lincoln PJ, Thomson J (eds) Forensic DNA profiling protocols. Humana, Totowa, pp 9–18

    Chapter  Google Scholar 

  • Woods JG, Paetkau D, Lewis D, McLellan BN, Proctor M, Strobeck C (1999) Genetic tagging of free-ranging black and brown bears. Wildl Soc B 27:616–627

    Google Scholar 

  • Yu N, Zheng CL, Zhang YP, Li WH (2000) Molecular systematics of pikas (genus Ochotona) inferred from mitochondrial DNA sequences. Mol Phylogenet Evol 16:85–95

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgements

We would like to thank L. Evans, B. Granger, D. Rissling, Z. Sim, A. Goodwin, K. Hayhurst, D. Kuch and S. and A. Henry for assistance in the field. K. Galbreath kindly provided pika liver samples from the Bella Coola valley. Thanks to A. Gonçalves da Silva and K. Larsen for interesting discussions that contributed to the design of this noninvasive genetic sampling method. C. Miño, A. Arnall, A. Gonçalves da Silva, C. Ray, M. Peacock and two anonymous reviewers are thanked for valuable comments on the manuscript. This work was funded by the Natural Sciences and Engineering Research Council of Canada Discovery and UBC Okanagan Individual Research grants to MAR. A Swiss National Science Foundation Doctoral Fellowship PBSKP3_128523 supported PH. This study was undertaken following the animal care protocol from the University of British Columbia (certificate number A07-0126).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Philippe Henry.

Additional information

Communicated by C. Gortázar

Electronic supplementary materials

Below is the link to the electronic supplementary material.

Table S1

Information regarding mitochondrial cytochrome b fragments amplified, including fragment names, primer names and sequences as well as overall length of fragment amplified. (DOC 32 kb)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Henry, P., Russello, M.A. Obtaining high-quality DNA from elusive small mammals using low-tech hair snares. Eur J Wildl Res 57, 429–435 (2011). https://doi.org/10.1007/s10344-010-0449-y

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10344-010-0449-y

Keywords

Navigation