ISSN: 0973-7510

E-ISSN: 2581-690X

Masoomeh Shemshad1, Khadijeh Shemshad2, Mohammad Mehdi Sedaghat3 and Javad Rafinejad3,4
1Department of Agricultural Extension and Education, Science and Research Branch,
Islamic Azad University, Tehran, Iran.
2Department of Entomology, Science and Research Branch, Islamic Azad University, Tehran, Iran.
3Department of Medical Entomology and Vector Control, School of Public Health,
Tehran University of Medical Sciences, Tehran, Iran.
4Evaluation Management and Development Center, Deputy of Research Ministry of Health and Medical Education, Tehran, Iran.
J Pure Appl Microbiol. 2012;6(2):627-632
© The Author(s). 2012
Received: 06/04/2012 | Accepted: 14/05/2012 | Published: 30/06/2012
Abstract

A total of 165 blood samples were collected in k2EDTA-containing tubes and thin and thick smears of domestic ruminants were prepared. Direct sequencing of polymerase chain reaction for detection of Theileria spp. using specific oligonucleotide primers was performed on 18s rRNA gene sequence of the parasite in Qazvin province. Of the 165 field samples obtained from domestic ruminants in the study area tested, 9.69% (16) were positive for the presence of Theileria spp. by PCR and 2.42% by microscopic examination for Theileria spp. in field-collected. Out of 165 positive blood samples, 4.24% were positive for Theileria annulata and 5.45% were positive for Theileria ovis by PCR. The lowest detection limit of the PCR was two parasites per ml of infected blood, which corresponds with a parasitemia of 0.00004%. Results of the molecular study revealed that Theileria ovis is widespread in sheep and its prevalence was higher than Theileria annulata.

Keywords

Theileria annulata, Theileri ovis, domestic ruminants, PCR

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