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Development and Evaluation of Real-Time RT-PCR Test for Quantitative and Qualitative Recognition of Current H۹N۲ Subtype Avian Influenza Viruses in Iran

عنوان مقاله: Development and Evaluation of Real-Time RT-PCR Test for Quantitative and Qualitative Recognition of Current H۹N۲ Subtype Avian Influenza Viruses in Iran
شناسه ملی مقاله: JR_ARCHRAZI-73-3_002
منتشر شده در در سال 1397
مشخصات نویسندگان مقاله:

S. G. Mirzaei - Department of Avian Bacterial Diseases, Research and Diagnosis, Razi Vaccine and Serum Research Institute, Agricultural Research, Education, and Extension Organization, Karaj, Iran
A. Shoushtari - Department of Avian Viral Diseases, Razi Vaccine and Serum Research Institute, Agricultural Research, Education, and Extension Organization, Karaj, Iran
A. Nouri - Department of Avian Bacterial Diseases, Research and Diagnosis, Razi Vaccine and Serum Research Institute, Agricultural Research, Education, and Extension Organization, Karaj, Iran

خلاصه مقاله:
Avian influenza H۹N۲ subtype viruses have had a great impact on Iranian industrial poultry production economy since introduction in the country. To approach Rapid and precise identification of this viruses as control measures in poultry industry, a real time probe base assay was developed to directly detect a specific influenza virus of H۹N۲ subtype -instead of general detection of Influenza A viruses- which has been endemic over two last decades in the country. An Iranian avian influenza virus strain of A/Iran/chicken/۷۷۲/۱۹۹۸ H۹N۲ subtype were selected as reference strain for of primers and probe designing. The high agreement value of ۹۹% indicated that the devolved real time assay for detection of H۹ subtype viruses could easily replace the conventional method of virus isolation particularly in investigation of viruses like national surveillance plan. The limit of detection was almost one EID۵۰ which was the least real infectious unit could be detected. So it can be said that this sensitive assay provided a powerful tool to not to miss any significant viral biological activity neither in the host body nor in the environment. A high level of correlation coefficient (R۲ = ۰.۹۹۸) also indicated a good correlation between Ct values and viral concentrations. , it can be conclude that the real time RT-PCR could be easily replace virus isolation in detection of H۹N۲ influenza viruses especially in large monitoring program. The ability in quantifying of the virus concentration extends usage of test in more accurate studies.

کلمات کلیدی:
Real-Time RT- PCR, Avian Influenza, Comparison, H۹N۲, Culture

صفحه اختصاصی مقاله و دریافت فایل کامل: https://civilica.com/doc/1868678/