“…Universal primers were defined in conserved regions (exons) and were used to amplify mtDNA regions with conserved microsynteny. Polymorphism in amplified fragment has been revealed with various methods: PCR-RFLP (Boonruangrod et al, 2008;Godbout et al, 2005;San Jose-Maldia et al, 2009;Moriguchi et al, 2009;Naydenov et al, 2007), RFLP-SSR (Burban and Petit, 2003;Godbout et al, 2005;Jaramillo-Correa et al, 2003), mtDNA-SSR (Hosaka and Sanetomo, 2009), the variable number of tandem repeats (VNTR) in minisatelite regions (Bastien et al, 2003;Fievet et al, 2007;Honma et al, 2011;Yoshida et al, 2012), and finally in DNA sequences (Avtzis and Aravanopoulos, 2011;Eckert et al, 2008;Edwards et al, 2005;Goodall-Copestake et al, 2010;Gugger et al, 2011). The choice of the candidate loci was limited and was depending on the taxonomic level addressed by the phylogenetic study.…”