Abstract

In Western countries dogs and cats are the most popular pets, and people are increasingly opposed to their rearing for the fur industry. In 2007, a Regulation of the European Union (EU) banned the use and trade of dog and cat furs, but an official analytical protocol to identify them as source species was not provided, and violations of law are still frequent in all Member States. In this paper we report on the development and validation of a simple and affordable DNA method for species detection in furs to use as an effective tool to combat illegal trade in fur products. A set of mitochondrial primers was designed for amplification of partial cytochrome b, control region and ND1 gene in highly degraded samples, like furs and pelts. Our amplification workflow involved the use of a non-specific primer pair to perform a first test to identify the species through sequencing, then the application of species-specific primer pairs to use in singleplex end-point PCRs as confirmation tests. The advantage of this two-step procedure is twofold: on the one hand it minimises the possibility of negative test results from degraded samples, since failure of amplification with a first set of primers can be offset by successful amplification of the second, and on the other it adds confidence and reliability to final authentication of species. All designed primers were validated on a reference collection of tissue samples, obtaining solid results in terms of specificity, sensitivity, repeatability and reproducibility. Application of the protocol on real caseworks from seized furs yielded successful results also from old and dyed furs, suggesting that age and chemical staining do not necessarily affect positive amplifications. Major pros of this approach are: (1) sensitive and informative primer sets for detection of species; (2) short PCR amplicons for the analysis of poor quality DNA; (3) binding primers that avoid contamination from human DNA; (4) user-friendly protocol for any laboratory equipped for analysis of low-copy-number DNA. Our molecular procedure proved to be a good starting point for enforcing the EU Regulation against dog and cat fur trade in forensic contexts where source attribution is essential to the assignment of responsibilities.

Highlights

  • About 55 million animals are assumed to die every year for their fur (Kerswell, 2009)

  • DNA testing on reference samples DNA from all specimens of the reference species were tested with primers furND1

  • No amplification occurred in P. lotor, L. europaeus and H. sapiens

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Summary

Introduction

About 55 million animals are assumed to die every year for their fur (Kerswell, 2009). In Western countries, dogs and cats are the most popular and beloved companion pets People find it unacceptable to farm these animals for their furs, nor do they want to inadvertently buy products containing such fur. Dog and cat fur trade is a thriving market in many Asian countries, China in particular, where the rearing of these domestic species for fur-pelt industry is practiced legally, and where laws on animal welfare are lacking. Following the autonomous initiative of some European countries, the EU officially banned the import to or the export from all Member States of dog (Canis lupus familiaris) and cat (both domestic and non-domestic Felis silvestris) furs, and all products containing fur from these animals, with a Regulation (n.1523) dated 2007 (European Parliament, 2007). The Regulation allowed that the rules on type and severity of penalties to infringements of the provisions were laid down under each national law

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