Molecular Study of Sheep Malignant Theileriosis at Barka Region in the Sultanate of Oman

Background: We used the PCR technique based on the abovementioned primer pair and sequenc­ing to demonstrate the Theileria infection in the sheep samples collected from Sultanate of Oman.Methods: According to the frame work of "integrated control of ticks and tick borne diseases in global­ized world managed by EU-ICTTD-3 project, the samples from blood, liver, spleen, lymph node and lung were sent to the laboratory of Iranian Research Center for Ticks and Tick-borne Diseases (IRCTTD). Sam­ples from blood smear and impression smears from liver, spleen, lymph node, and lung were analyzed by Geimsa staining. The DNA was extracted from the abovemen­tioned samples and analyzed by PCR tech­nique using specific primers derived from the nucleo­tide sequences of 18S rRNA gene of T. lestoquardi, which can amplify the common region in other Theileria and Babesia spp. Subsequently the amplified DNA was sequenced.Results: The analysis of blood smears of the sheep was negative for piroplasmosis performed through the Giemsa staining. The impression smears prepared from liver, spleen, lymph node, and lung showed suspi­cious structures mimicking Theileria schizonts in some cells. The results showed an expected PCR prod­uct of 428 bp in length, which is specific for Theileria spp. The PCR products were subsequently se­quenced. The corresponding nucleotide sequence is registered under accession number JF309152 in Gen­Bank. The sequence alignment in GenBank showed that the PCR products had 99% homology to the known T. lestoquardi registered under accession number AF081135 in the GenBank. Conclusion: Oman sheep are highly susceptible for Theileria infection and the infected sheep mostly die before the microschizonts or erythrocytic form of Theileria appears in the nucleated or ery­trocytic cells respectively

In vitro expression of apocarotenoid genes in Crocus sativus L.

Calli were successfully induced from style explants of Crocus sativus L. on Murashige and Skoog's medium supplemented with -naphthalene acetic acid and 6-benzylaminopurine. Then they were divided into three different types based on developmental stages and pigmentation progress in induced stigma-like structures. RT-PCR method was set up using calli in different developmental stages to detect expression levels of CsLYC, CsBCH1, CsZCD and CsUGT2 genes for apocarotenoids biosynthesis via mevalonic acid pathway in C. sativus. The results obtained from in vitro investigationof CsUGT2 expression levels in all three developmental stages were analyzed and compared with the expression levels of selected genes carried out on intact stigmas in vivo. Apparently, this gene was only expressed in the stage III of the three in vitro different SLSs developmental stages. Furthermore,the expression levels of CsLYC, CsBCH1, CsZCD were detected in stage III with fully developed SLSs and were comparable with those of in red intact stigmas