A Noninvasive Hair Sampling Technique to Obtain High Quality DNA from Elusive Small Mammals

1. Hair snare

Prior to setting up a snare, an ideal location has to be determined within the pika habitat or talus slope. This includes hay piles, which are vegetation caches that the animals collect in late summer as well as fresh scats found at latrine sites. Strips of packing tape (10-50cm in length) are rolled up to provide a 360° sticky surface and are arranged in a web-like manner to envelope the entrance to the pika’s hay pile (Fig. 1) or latrine site. Depending on the configuration of the rocks, a piece of fishing line may be used to support the structure of the hair snare, but this is often not necessary when entrances are quite small (<30cm in diameter), a complete description of the use of fishing line can be found in Henry and Russello (2010)³. Hair snares are checked as often as possible, and hair samples deposited on the tape (Fig. 2) are then collected and labeled. Once transported back to the lab, hairs are removed from the sticky tape using sterile forceps and transferred into cryogenic tubes and stored at -20°C until further manipulation. Hair samples clustered together along a hair snare are considered to belong to a single individual, while samples clustered independently are assumed to belong to different individuals. In the latter case, the hair is then placed in different tubes. These assumptions can later be tested by way of DNA fingerprints and calculations of probability of identity based on microsatellite genotypic data.

2. DNA extraction

Since pika hair is very thin and contains a tiny root bulb, we have previously shown that a minimum of 25 hairs are required to obtain sufficient amounts of DNA for good quality downstream PCR amplification³. We used the DNA IQ system (Promega, Madison, WI, USA) and a slightly modified version of the manufacturer’s instructions for DNA isolation from hair samples. Firstly, the hair sample is spun down in a micro-centrifuge in order to avoid loss of hair while opening the tube. Then the incubation solution is prepared by mixing 80 μl of incubation solution with 10μl of DTT (1M) and 10μl of Proteinase K (18ng/ml) to result in a final concentration of 0.1 M DTT and 1.8ng/ml of Proteinase K. Incubation solution (100 μl) is added to the sample and incubated at 56°C for 1 hour. In the meantime, the lysis solution is prepared by adding 1 μl of DTT (1M) for every 100 μl of lysis buffer, resulting in a final DTT concentration of 0.01M. Prepared lysis solution (200 μl) is then added to the sample, along with 7 μl of DNA IQ resin, vortexed for 3 seconds at high speed and incubated at room temperature for 5 minutes. The sample is then vortexed for 2 seconds and inserted in the magnetic stand, where separation of magnetic beads from the solution occurs. The remaining solution is then aspirated and discarded, being careful not to disturb the pellet of magnetic resin. The sample is then treated with 100 μl of the prepared lysis solution, vortexed and returned to the magnetic stand where separation occurs again. The lysis buffer is aspirated and discarded, and this step is repeated three times using a wash buffer (100 μl). The sample is subsequently left to dry in the magnetic stand for 15 minutes. Once dry, 100 μl of elution buffer is added to the sample and incubated at 65 °C for 5 minutes. The sample is vortexed and inserted into the magnetic stand. The solution now containing the eluted DNA is then transferred to a 1.5 ml Eppendorf tube and stored at -20°C until further manipulations. DNA from liver samples was also extracted using the DNA IQ system and used as a positive control for PCR amplifications.

3. PCR amplification

The DNA obtained from our noninvasive hair snare and liver samples were then used to amplify a suite of commonly used molecular markers (microsatellite, AFLP, mitochondrial cytochrome B and ZFX/ZFY sexing marker). PCRs were performed using a Veriti thermal cycler (Applied Biosystems, Foster City, CA, USA) in a 25 μL volume containing: 10 – 20 ng DNA, 0.5 μM of each primer, 10 mM Tris-HCl (pH 8.3), 50 mM KCl, 1.5 mM MgCl₂, 200 μM dNTPs, 10 μ bovine serum albumin (BSA; New England Biolabs, Ipswich, MA, USA) and 0.5 U AmpliTaq Gold DNA polymerase (Applied Biosystems). Cycling parameters for the microsatellite loci were optimised using a touchdown cycling program (10 min at 95°C, 35 cycles at 95°C for 30 s, 30 s annealing, and 45 s at 72°C, followed by a final step at 72°C for 10 min). The annealing temperature decreased by 1°C per cycle from 60 to 55°C until reaching the sixth cycle, at which point the 29 remaining cycles continued at 55°C. Cycling parameters for the mitochondrial fragments were as described above but consisted of 35 cycles with an annealing temperature of 50°C. Amplified Fragment Length Polymorphism was undertaken following the protocol for vertebrate genomes described by Bonin⁴. Lastly, molecular sexing was undertaken using the PCR-RFLP of ZFX/ZFY loci with HinfI restriction enzyme digestion⁵. The PCR products from the microsatellite, AFLPs and cytochrome B sequences were run onto a ABI 3130XL genetic analyser (Applied Biosystems), while digested ZFX/ZFX fragments were run alongside a 100 bp ladder (New England Biolabs) on a 3% agarose gel containing 2.5% SYBR Safe DNA gel stain (Invitrogen, Carlsbad, CA, USA) and visualised using a RED personal gel imaging system (Alpha Innotech, San Leandro, CA, USA). Microsatellite and AFLPs were visualized using Genemapper v3.7 (Applied Biosystems) and the mitochondrial DNA chromatogram was visualized using Sequencher v4.7 (Gene Code Corporation, Ann Harbour, MI, USA).

4. Representative results

The DNA extracted from hair samples obtained using our noninvasive snare were used to PCR amplify various type of molecular markers. As a basis for comparison, DNA extracted using liver samples was amplified alongside our hair samples. Nuclear microsatellite loci were successfully amplified for both hair and liver samples (Fig. 3). Although the intensity of the signal was greater when using the liver samples, this did not have an adverse effect on genotype scoring (Fig. 3). Similar results were achieved when using AFLPs (Fig. 4), mitochondrial DNA sequences (Fig. 5), and the ZFX/ZFY molecular sexing marker (Fig. 6).

Figure 1. An example of a noninvasive hair snare set up at a hay pile. Strips of rolled up clear packing tape are arranged in a web-like fashion to enclose the entrance to the hay pile. A piece of fishing line is used here to provide additional support for the hair snare.

Figure 2. A successful hair snare containing a large number of hair stuck to the packing tape.

Figure 3. A representative nuclear microsatellite chromatogram (Ocp6)⁸ as displayed in Genemapper v3.7 (Applied Biosystems). The top chromatogram was obtained by amplifying DNA from liver tissue, and is heterozygous (354/358) at this locus. The bottom chromatogram represents a different individual exhibiting a heterozygous genotype (358/362) based on DNA extracted from hair. While the signal of chromatogram from the hair sample has a lower intensity than the liver sample, genotype scoring is not adversely affected by this difference in signal.

Figure 4. A representative AFLP chromatogram (E31T32) as displayed in Genemapper v3.7 (Applied Biosystems). The top chromatogram was obtained by amplifying DNA from liver tissue, the bottom chromatogram represents the DNA extracted from hair.

Figure 5. A representative mitochondrial DNA sequence chromatogram (cytochrome B) as displayed in Sequencher v4.7 (Gene Code Corporation). The top chromatogram was obtained by amplifying DNA from liver tissue, the bottom chromatogram represents the DNA extracted from hair.

Figure 6. A representative molecular sexing marker (ZFX/ZFY) amplified for both liver and hair samples. This approach relies on the observation that the Y chromosome possesses a HinfI restriction site in this region that the X chromosome lacks. Thus, females produce two co-migrating fragments of 432 bp while males produce fragments of 432 bp, 261 bp and 171 bp.