“…Data pertaining to the ribosomal RNA (rRNA) gene sequences–in particular, the two non-coding, highly variable internal transcribed spacer regions (ITS1 and ITS2) are considered to be acceptable molecular criteria for resolving taxonomic questions and determining the phylogenetic affinities among closely related Leishmania species [17,21-25]. While coding genes are also wildly used for taxonomic studies, such as metabolic enzymes (ICD, ME, MPI, G6PDH, ASAT, GPI, NH1, NH2, PGD and FH) [26,27], heat-shock protein 70 gene (hsp70) [4], cytochrome oxidase II (CO II) [28], the gene encoding the largest subunit of RNA polymerase II (rpoIILS) [6,8], the glycoprotein 63 gene ( gp 63) [29], cysteine protease B genes ( cpb ) [30] and cytochrome b (cyt b ) [31-35]. …”