Pathogenicity study of Iranian genotype of avian infectious bronchitis virus (IR-۱)

  • سال انتشار: 1396
  • محل انتشار: گفتمان پژوهش دامپزشکی، دوره: 8، شماره: 1
  • کد COI اختصاصی: JR_VRFAN-8-1_006
  • زبان مقاله: انگلیسی
  • تعداد مشاهده: 69
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نویسندگان

Hamideh Najafi

Department of Microbiology and Immunology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran

Arash Ghalyanchi-langeroudi

Department of Microbiology and immunology, Faculty of Veterinary Medicine, University of Tehran, Tehran

Masoud Hashemzadeh

Department of Research and Production of Poultry Viral Vaccine, Razi Vaccine and Serum Research Institute, Karaj, Iran

Vahid Karimi

Department of Poultry Diseases, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran

Omid Madadgar

Department of Microbiology and Immunology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran

Reza Khaltabadi Farahani

Iranian veterinary Organization, Tehran, Iran

Seyed Ali Ghafouri

Iranian veterinary Organization, Tehran, Iran

Hossein Maghsoudloo

Iranian veterinary Organization, Tehran, Iran

Parvaneh Seifouri

Iranian veterinary Organization, Tehran, Iran

Ali Madhi

Department of Microbiology and Immunology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran

چکیده

Avian infectious bronchitis (IB) is a major cause of economic losses in poultry industry. The IB virus primarily affects respiratory tract, but various strains differ in their tropism for other target organs such as kidney and alimentary tract. The objective of this study was to estimate the pathogenicity of Iranian IBV variant (IR-۱), which is limited exclusively to Iran. Specific pathogen free chicks were inoculated intranasally. Sera, fecal swabs and different tissue samples were collected on different days post infection (DPI). Clinical signs, gross pathology and histological changes were recorded. The viral load was quantified in the RNA extractions from different tissue samples using real-time PCR. Anti-IBV antibodies were detected in serum samples. The IgG antibody were found on ۲۱ and ۲۸ DPI. Severe histological lesions were observed in the trachea and lung while the lesions in kidney were appeared to be milder. Viral RNA was detected in all tested tissues from ۱ DPI to the last day of the experiment. The highest viral load was measured in the trachea and feces on ۱st and ۵th DPI, respectively. It can be concluded the IR-۱ had broad tropism for respiratory tract, digestive system, and renal tissue, reflecting its epitheliotropic nature, but it caused the most severe lesions in the respiratory tract. This was the first pathogenicity study of Iranian IR-۱ IBV. Further knowledge of IBV pathogenesis provides the groundwork to inform more effective prevention practices.

کلیدواژه ها

Avian infectious bronchitis, Biochemical analysis, Histopathology, pathogenesis, Real-time PCR

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