Mirzaei S G, Shoushtari A, Nouri A
Department of Avian Bacterial Diseases, Research and Diagnosis, Razi Vaccine and Serum Research Institute, Agricultural Research, Education, and Extension Organization, Karaj, Iran.
Department of Avian Viral Diseases, Razi Vaccine and Serum Research Institute, Agricultural Research, Education, and Extension Organization, Karaj, Iran.
Arch Razi Inst. 2018 Sep;73(3):177-182. doi: 10.22092/ari.2017.106968.1059. Epub 2018 Sep 1.
Avian influenza H9N2 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 H9N2 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/772/1998 H9N2 subtype were selected as reference strain for of primers and probe designing. The high agreement value of 99% indicated that the devolved real time assay for detection of H9 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 EID50 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 (R2 = 0.998) 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 H9N2 influenza viruses especially in large monitoring program. The ability in quantifying of the virus concentration extends usage of test in more accurate studies.
自H9N2亚型禽流感病毒传入伊朗以来,对该国的工业家禽生产经济产生了巨大影响。为了在禽类产业中作为控制措施快速准确地鉴定这种病毒,开发了一种实时探针检测法,以直接检测H9N2亚型的特定流感病毒,而不是检测甲型流感病毒,在过去二十年中,该病毒在该国一直呈地方流行。选择一株伊朗A/Iran/chicken/772/1998 H9N2亚型禽流感病毒株作为引物和探针设计的参考菌株。99%的高一致性值表明,用于检测H9亚型病毒的实时检测法可以轻松取代传统的病毒分离方法,特别是在像国家监测计划这样的病毒调查中。检测限几乎为1个EID50,这是能够检测到的最低实际感染单位。因此,可以说这种灵敏的检测法提供了一个强大的工具,不会错过宿主体内或环境中任何显著的病毒生物学活性。高相关系数(R2 = 0.998)也表明Ct值与病毒浓度之间具有良好的相关性。可以得出结论,在检测H9N2流感病毒时,实时RT-PCR可以轻松取代病毒分离,特别是在大型监测项目中。定量病毒浓度的能力扩大了该检测方法在更精确研究中的应用。