“…The use of molecular sequence techniques is providing a large amount of additional data for phylogenetic analyses, but in spite of this, evolutionary relationships remain to be solved (Hughes and Piontkivska, 2003). Different molecular markers have been used for phylogenetic studies in Leishmania: the internal transcribed spacer (ITS) 1 and 2 of the ribosomal DNA array (Cupolillo et al, 1995;Dávila and Momen, 2000;Berzunza-Cruz et al, 2002;Orlando et al, 2002;Kuhls et al, 2005;Spanakos et al, 2008;Sukmee et al, 2008;Villinski et al, 2008), a repetitive DNA sequence (Piarroux et al, 1995), the gene for DNA polymerase α catalytic subunit (POLA, Croan et al, 1997), the gene encoding the largest subunit of RNA polymerase II (RPOIILS, Croan and Ellis, 1996;Croan et al,1997), the cytochrome oxidase II gene (COII, Ibrahim and Barker, 2001;Cao et al, 2011), the glycoprotein 63 gene (gp63, Mauricio et al, 2007), cysteine protease B genes (cpb, Hide et al, 2007), the mini-exon (Sukmee et al, 2008), 7SL RNA (Zelazny et al, 2005;Guan et al, 2012), the small subunit ribosomal RNA (SSU rRNA, Guan et al, 2012), and the cytochrome B gene (cytB, LuyoAcero et al, 2004;Asato et al, 2009). Recently, Boité et al (2012) evaluated the phylogeny of Leishmania (Viannia) parasites based on multilocus sequence analysis using different housekeeping genes.…”