loading page

Fast-tracking bespoke DNA reference database generation from museum collections for biomonitoring and conservation
  • +4
  • Andrew Dopheide,
  • Talia Brav-Cubitt,
  • Anastasija Podolyan,
  • Rich Leschen,
  • Darren Ward,
  • Thomas Buckley,
  • Manpreet K. Dhami
Andrew Dopheide
Landcare Research New Zealand Auckland

Corresponding Author:dopheidea@landcareresearch.co.nz

Author Profile
Talia Brav-Cubitt
Landcare Research New Zealand Auckland
Author Profile
Anastasija Podolyan
Landcare Research New Zealand
Author Profile
Rich Leschen
Landcare Research New Zealand Auckland
Author Profile
Darren Ward
Landcare Research New Zealand Auckland
Author Profile
Thomas Buckley
Landcare Research New Zealand Auckland
Author Profile
Manpreet K. Dhami
Landcare Research New Zealand
Author Profile

Abstract

Despite recent advances in high-throughput DNA sequencing technologies, a lack of locally relevant DNA reference databases may limit the potential for DNA-based monitoring of biodiversity for conservation and biosecurity applications. Museums and national collections represent a compelling source of authoritatively identified genetic material for DNA database development yet obtaining DNA barcodes from long-stored specimens may be difficult due to sample degradation. We demonstrate a sensitive and efficient laboratory and bioinformatic process for generating DNA barcodes from hundreds of invertebrate specimens simultaneously via the Illumina MiSeq system. Using this process, we recovered full-length (334) or partial (105) COI barcodes from 439 of 450 (98 %) national collection-held invertebrate specimens. This included full-length barcodes from 146 specimens which produced low-yield DNA and no visible PCR bands, and which produced as little as a single sequence per specimen, demonstrating high sensitivity of the process. In many cases, the identity of the most abundant sequences per specimen were not the correct barcodes, necessitating the development of a taxonomy-informed process for identifying correct sequences among the sequencing output. The recovery of only partial barcodes for some taxa indicates a need to refine certain PCR primers. Nonetheless, our approach represents a highly sensitive, accurate, and efficient method for targeted reference database generation, providing a foundation for DNA-based assessments and monitoring of biodiversity.
19 May 2022Submitted to Molecular Ecology Resources
01 Jun 2022Submission Checks Completed
01 Jun 2022Assigned to Editor
07 Jun 2022Reviewer(s) Assigned
02 Aug 2022Review(s) Completed, Editorial Evaluation Pending
03 Aug 2022Editorial Decision: Revise Minor
22 Sep 2022Review(s) Completed, Editorial Evaluation Pending
22 Sep 20221st Revision Received
06 Oct 2022Editorial Decision: Revise Minor
17 Oct 20222nd Revision Received
17 Oct 2022Review(s) Completed, Editorial Evaluation Pending
25 Oct 2022Editorial Decision: Accept
21 Nov 2022Published in Molecular Ecology Resources. 10.1111/1755-0998.13733