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Background <p>Non-invasive genetic monitoring is essential for conserving the endangered Asian elephant (<i>Elephas maximus</i>). However, fecal DNA is highly susceptible to degradation and polymerase chain reaction (PCR) inhibition.</p> Objective <p>Various DNA extraction techniques and optimized downstream PCR parameters were compared to establish a workflow that balances DNA quantity and quality.</p> Methods <p>A modified phenol–chloroform–isoamyl alcohol (PCI) protocol was compared with a commercial extraction kit using 35 unpreserved, degraded fecal specimens to evaluate the trade-offs between DNA yield and purity.</p> Results <p>The PCI method produced significantly higher concentrations (&gt; 500&#xa0;ng/µL in some samples) but poor purity ratios (A<sub>260</sub>/A<sub>280</sub> and A<sub>260</sub>/A<sub>230</sub>), resulting in complete PCR failure. In contrast, the kit yielded lower DNA amounts but superior purity (A<sub>260</sub>/A<sub>230</sub> = 2.0–2.2), enabling a 57.1% (20/35) amplification success rate for the mitochondrial D-loop when combined with high-processivity KOD polymerase and optimized Mg<sup>2</sup>⁺ concentrations. Sanger sequencing confirmed <i>E. maximus</i> mitochondrial DNA in 15 specimens, whereas environmental eDNA was detected in two samples.</p> Conclusion <p>These findings demonstrate that DNA purity, rather than yield, is the critical determinant of PCR success in degraded wildlife samples, underscoring the importance of inhibitor-removal technologies for the reliable and effective management of endangered megafauna.</p>

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DNA purity over yield: optimizing extraction and PCR in degraded Asian elephant (Elephas maximus) fecal samples

  • 期刊论文

  • 发表日期：

    2026年5月19日

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  • Supansa Rerkdee,
  • Worapong Singchat,
  • Thitipong Panthum,
  • Trifan Budi,
  • Warong Suksavate,
  • Aingorn Chaiyes,
  • Wichanon Saenphala,
  • Kyudong Han,
  • Prateep Duengkae,
  • Kornsorn Srikulnath

摘要

Background

Non-invasive genetic monitoring is essential for conserving the endangered Asian elephant (Elephas maximus). However, fecal DNA is highly susceptible to degradation and polymerase chain reaction (PCR) inhibition.

Objective

Various DNA extraction techniques and optimized downstream PCR parameters were compared to establish a workflow that balances DNA quantity and quality.

Methods

A modified phenol–chloroform–isoamyl alcohol (PCI) protocol was compared with a commercial extraction kit using 35 unpreserved, degraded fecal specimens to evaluate the trade-offs between DNA yield and purity.

Results

The PCI method produced significantly higher concentrations (> 500 ng/µL in some samples) but poor purity ratios (A260/A280 and A260/A230), resulting in complete PCR failure. In contrast, the kit yielded lower DNA amounts but superior purity (A260/A230 = 2.0–2.2), enabling a 57.1% (20/35) amplification success rate for the mitochondrial D-loop when combined with high-processivity KOD polymerase and optimized Mg2⁺ concentrations. Sanger sequencing confirmed E. maximus mitochondrial DNA in 15 specimens, whereas environmental eDNA was detected in two samples.

Conclusion

These findings demonstrate that DNA purity, rather than yield, is the critical determinant of PCR success in degraded wildlife samples, underscoring the importance of inhibitor-removal technologies for the reliable and effective management of endangered megafauna.