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DNA Assay Aids in Identifying and Protecting North American Wolves, Coyotes

Gray Wolf
Gray Wolf. Image: Tracy Brooks, from USFWS digital library.

For Immediate Release

Forensics specialists can use a commercial assay targeting mitochondrial DNA to accurately discriminate between wolf, coyote and dog species, according to a new study from North Carolina State University. The genetic information can be obtained from smaller or more degraded samples, and could aid authorities in prosecuting hunting jurisdiction violations and preserving protected species.

In the U.S., certain wolf subspecies or species are endangered and restricted in terms of hunting status. It is also illegal to deliberately breed wolves or coyotes with domesticated dogs.

“If it’s a case where you have a whole specimen, authorities can typically identify it based on physical characteristics, though similarity between some species makes that method less than ideal,” says Kelly Meiklejohn, assistant professor of forensic science at NC State and corresponding author of the research. “If you’re working with cross-bred animals, or incomplete specimens, you need DNA-based methods to accurately determine what species you have.”

Although some U.S. federal laboratories perform DNA-based identification of wolves and coyotes, their methods and genetic reference databases aren’t publicly available. Meiklejohn partnered with the U.S. Fish and Wildlife Service to see if it was possible to use a commercially available assay designed for dogs as a way to recover the mitochondrial genome from diverse North American canid species.

The mitochondrial genome is one of two genomes inherited from an animal’s parents. Specifically, the mitochondrial genome is inherited from the mother. It is useful for species identification both because its circular shape makes it less prone to degradation, and because there are more copies of this genome per cell, increasing the chance of retrieving useful material from small or damaged samples.

The team used a method, called a ‘hybridization capture,’ in which about 80 base-pair long RNA fragments are used to isolate DNA for sequencing. Samples are incubated with the RNA fragments, and if there’s a match, the fragment will bind with the sample’s DNA. The bound DNA can be isolated and sequenced. In this case, the team used a hybridization capture panel designed for the dog mitochondrial genome.

“The fragments will bind if there is about 80% similarity, which is why we felt the dog kit would be useful for sequencing wolves and coyotes,” Meiklejohn says. “Dogs only diverged from wolves around 20,000 years ago, so the mitochondrial genomes aren’t that different.”

They sequenced 51 samples, and were able to recover full mitochondrial genomes and successfully differentiate between four species of interest: dog, wolf, Mexican wolf, and coyote.

“Essentially, this finding means we can do more with less,” Meiklejohn says. “In forensics we rarely have high quality DNA samples; they’ve usually been exposed to the environment and are degraded. The flexibility of this kit allows us to determine the species we’re looking at, which in turn may aid in prosecuting hunting or breeding violations and protecting endangered canid species.”

The research appears in Forensic Science International: Animals and Environments, and is supported by seed funding from NC State. Dyan Straughan and Mary Burnham-Curtis, from the U.S. Department of the Interior, Fish and Wildlife Service, are coauthors.

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Note to editors: An abstract follows.

“Using hybridization capture to obtain mitochondrial genomes from forensically relevant North American canids: assessing sequence variation for species identification”

DOI: 10.1016/j.fsiae.2021.100018

Authors: Melissa Scheible, Kelly Meiklejohn, North Carolina State University; Dyan Straughan, Mary Burnham-Curtis, U.S. Department of the Interior, Fish and Wildlife Service
Published: June 25, 2021 in Forensic Science International: Animals and Environments

Abstract:
The majority of DNA casework processed by forensic laboratories focuses on human samples, but material from canids (dogs, wolves, coyotes) can also be encountered. Undomesticated canids can be the center of forensic investigations in the U.S. since some species are endangered. As many wolf species are similar morphologically, identification in the field by wildlife officers is not always straight-forward, making molecular based-approaches ideal. While some published methods using mitochondrial DNA targets can discriminate among Canis species, they are either not compatible with highly degraded samples or cannot differentiate closely related sub-species. Although some U.S. laboratories regularly perform veterinary/wildlife casework including canid identifications, their validated methods and reference genetic databases are not publicly available. We aimed to assess the utility of alternative regions in the mitochondrial genome for discriminating among canid species, including the complete genome. To achieve this, we utilized a commercial hybridization capture panel composed of biotinylated RNA “baits” designed for the domestic dog to enrich canid mitochondrial genomes for next-generation sequencing. We used this panel to successfully sequence complete mitochondrial genomes for 51 samples, representing four U.S. forensically relevant canids (coyote, wolf, Mexican wolf, dog). While the complete mitochondrial genome permitted discrimination, we also assessed previously published mitochondrial DNA targets (n, 5) for resolution and identified four alternate ~200 bp fragments from ND1, ND5, COI and CYTB genes that could help resolve canids. The utility of these alternate regions should be assessed in future studies using forensic-type samples representing canids from diverse geographic areas, prior to casework implementation.

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