Author : A'aiz, N.N.


Genotyping of cystic echinococcosis isolates from clinical samples of human and domestic animals

S.A. Fadhil; N.N. A'aiz

Iraqi Journal of Veterinary Sciences, 2016, Volume 30, Issue 2, Pages 33-39
DOI: 10.33899/ijvs.2016.121381

Cystic hydatid disease is a cosmopolitan important disease in both human and animals. Many strains were investigated in this parasite. The aim of study was to characterize genotype variations of Echinococcus granulosus isolates collected from human and domestic animals in Al-Qadisiyah province/ Iraq based on sequencing of nad1 mitochondrial gene. Eighty hydatid cysts of human (12), sheep (15), cattle (36), and camels (17) were collected from hospital and slaughter house of the province, during October 2014 to June 2015; microscopic examination was made for cysts fluid to determine the fertility. DNAs extraction was done for each sample in addition to purify and concentrate of extracted DNA samples was performed to determine nad1 (400bp) gene used conventional PCR method. Phylogenetic analysis was performed using NCBI-Blast Alignment identification and Unweighted Pair Group Method with Arithmetic Mean. Twenty five (10 from human and 5 from each studied animals) samples were chosen due to their fertility and high DNA purity, in which three strains (genotypes) were investigated including sheep strain (G1) 40%, buffalo strain (G3) 48% and camel strain (G6) 12%, where human samples related to G1(20%) and G3(80%); sheep samples related to G1(80%) and G3(20%); cattle samples related to G1(60%), G3 (20%) and G6 (20%); camels samples related to G1(20%), G3(40%) and G6(40%). The dominant strain is a buffalo strain (G3); both of buffalo strain (G3) and sheep strain (G1) represented the actual source of human infection. There is no host specificity of detected genotypes.

Determination of Toxoplasma gondii lineages of sheep in Wasit, Iraq

N.N. A'aiz

Iraqi Journal of Veterinary Sciences, 2016, Volume 30, Issue 2, Pages 23-26
DOI: 10.33899/ijvs.2016.121379

Toxoplasma gondii is an intracellular parasite that can cause significant morbidity in human beings and animals. Up to our knowledge no data is known of genetic diversity of T. gondii in sheep in Iraq. This study aim to detect the strains (genotypes) of T. gondii isolates from sheep in Wasit province, east of Iraq. A total of 315 samples (blood 300 and placenta's tissue 15) were collected from aborted ewes, which initially had been examined serologically by LAT, then further tested by RT-PCR through B1 gene amplification to confirm the infection with T. gondii. After that, the positive DNA samples were assayed for genetic characterization depending upon nested PCR- RFLP of SAG2 gene. Out of 315 examined samples, 10 were confirmed positive T. gondii DNA. The genotyping assay of them revealed that 60% (6/10), 30% (3/10) and 10% (1/10) of examined isolates represent the genotypes of II, III and I respectively. The type II appeared as dominant in sheep in Wasit province, Iraq.

Phylogenetic study of Theileria lestoquardi based on 18SrRNA gene Isolated from sheep in the middle region of Iraq

M.J.A. Alkhaled; N.N. A'aiz; H.H. Naser

Iraqi Journal of Veterinary Sciences, 2016, Volume 30, Issue 2, Pages 27-32
DOI: 10.33899/ijvs.2016.121380

Theileriosis is parasitic infection causes by obligate intracellular protozoa of the genus Theileria. T. lestoquardi is the most virulent species in sheep and goats which causes a severe disease with a high morbidity and mortality rate. In this study the phylogenetic relationships between two local isolate of T. lestoquardi and nine T. lestoquardi global isolates as well as Babesia ovis out-group isolate were analyzed using the 18S rRNA gene sequence. The multiple sequence alignment analysis and neighbor joining phylogenetic tree analysis were performed by using ClustalW multiple sequence alignment online based analysis of 1098bp 18S rRNA gene was amplified by polymerase chain reaction. Phylogenetic analysis results of these gene sequences revealed that T. lestoquardi local isolates were closely related to T. lestoquardi Iran isolate (JQ917458.1) and two Iraq Kurdistan isolates (KC778786.1 and KC778785.1) more than other countries. This study represents the first report on the use of molecular phylogeny to classify T. lestoquardi obtained in Middle Region of Iraq.