سال انتشار: ۱۳۸۷
محل انتشار: اولین کنگره بین المللی مدیریت بهداشتی و بیماریهای آبزیان
تعداد صفحات: ۱
A Haghighi Khiabanian asl – Department of Aquatic Diseases, Faculty of Specialized Veterinary Sciences, Islamic Azad University of Iran, Science and Research Branch. Tehran,Iran
M Azizzadeh – General Manager of Aquatic Animal Health Department (IVO)
M Bandehpour – Cellular and Molecular Biology Research Center, Shahid Beheshti University, M.C., Tehran, Iran
Z. Sharifnia – Cellular and Molecular Biology Research Center, Shahid Beheshti University, M.C., Tehran, Iran
Method & Materials: The research samples were selected among Indian carps with the symptoms of SVC (kidney swallowing, exophthalmia, general petechiae, bronchi mottling, mouth inflammation, ascites, spotting bleeding on adipose tissues) under perishing between May 2006 and September 2007. Viral RNA extraction was done by RNX plus buffer as described by manufacturer (CinnaGen, Iran). Briefly, about 1 cubic mm of fish tissue was transferred to 1.5 ml micro tube, then 200 μl RNX plus buffer was added. The mixture was incubated for 5 min at 40C. Initial characterization of svcv cDNA clones was achieved by performing gapped BLASTN and BLASTX searches.
Results & Conclusion: Samples were screened by molecular and sequence analysis assays. In this research we confirmed the positive SVC in 3 Indian carps (Ruho, Merigal, catla catla) and sequencing DNA of genes in positive samples with confirmation in gene bank,and 2 sites in this research were placed in (Ahvaz) Khozestan and (Astaneh Ashrafieh) Gilan Aquaculture farms. University of Shahid Beheshti confirmed Mulecular tests with Nested–PCR and sequencing in gene bank with Blast software programe. It was the first transportation of Indian carp from foreign country to Iran. The results of this study indicate that SVC infection can be found in some Indian carp in Iran. To study the pathogenicity and to obtain isolates of SVC virus the establishment of a laboratory with virus culture equipment is necessary. The respect for on-site hygiene rules, control of disease in fish propagation and breeding centers, isolation and quarantining of infected Indian Carp or fish with abnormal behaviour have a major role for the prevention of disease. Often, one of the most important causes of little incidence of disease is also the weakness of viruscarriers. With Gene Sequencing technique, the virus genome is recognized perfectly.