Hydatid Cysts were obtained from 15 sheep from hepatic, pulmonary, spleen, heart, and peritoneal
cavity, between December 2014 and October 2015. Hydatid cysts (protoscoleces) were used for DNA
extraction by using mechanical grinder. The purification of mt DNA was done by (promega kit, USA).
The mitochondrial NADH dehydrogenase subunit 1 (ND1) genes was applied as aim for amplification by
using polymerase chain reaction (PCR), all of 15 hydatid cysts yielded amplification products.PCR
product for NADH1 800 bp. The PCR products had been purified and fractional sequences were
produced. The sequences obtained were found to align with corresponding region for ND1 gene in the
Gene Bank nucleotide database confirming to genotype of sheep strain (G1) in Iraq, Phylogenetic
dissection of fractional sequence datum from ND1 gene for obtained Phylogenetic tree. G1 genotype was
the majority widespread taxon and the genuine provenance of infection for Iraqi’s sheep. All of 15
specimens were G1 strain (sheep strain) according to the fractional sequences of NADH dehydrogenase 1
(ND1).