Isolation, molecular detection and BHK-21 adaptation of Newcastle disease virus of field cases in layer farms of Bangladesh
محل انتشار: مجله علمی میکروبیولوژی، دوره: 3، شماره: 6
سال انتشار: 1393
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 580
فایل این مقاله در 8 صفحه با فرمت PDF قابل دریافت می باشد
- صدور گواهی نمایه سازی
- من نویسنده این مقاله هستم
استخراج به نرم افزارهای پژوهشی:
شناسه ملی سند علمی:
JR_SJM-3-6_001
تاریخ نمایه سازی: 9 اسفند 1393
چکیده مقاله:
In this study, field samples (n=45) such as trachea, brain and proventriculus were collected from 12 layer farms of different districts of Bangladesh for the detection and isolation of pathogenic Newcastle disease virus (NDV). Isolation of the virus from the clinical samples and their propagation was primarily carried out in chicken embryo. Among the forty five samples, 9 (20%) were found positive for NDV by hemagglutination (HA) and hemagglutination inhibition (HI) tests. The positive isolates were cultured in chicken embryo, and subsequently confirmed by reverse transcription-polymerase chain reaction (RT-PCR) targeting NDV specific ‘F’ gene that encodes fusion protein. A nested PCR was carried out with the RT-PCR product as the template, which targeted a smaller internal region of ‘F’ gene. The nested PCR also confirmed all the isolates as NDV. For further confirmation, NDV specific ‘F’ gene was also amplified from the cDNA generated from the RNA extracted from the virus inoculated chicken embryo by direct PCR. The isolates were inoculated in BHK-21 cell line and 2/3 blind passage were given without any gross change in the cell. Later, the virus was found adapted into BHK-21 cell line where they produced syncitia, rounding of cell and multinucleated giant cells as the cytopathic effects. Adaptation of the virus in BHK-21 cell line was confirmed by RT-PCR and nested-PCR successfully
کلیدواژه ها:
نویسندگان
M.F.R. Khan
Department of Microbiology and Hygiene, Faculty of Veterinary Science, Bangladesh Agricultural University, Mymensingh- ۲۲۰۲, Bangladesh
S. Ahmed
Department of Microbiology and Hygiene, Faculty of Veterinary Science, Bangladesh Agricultural University, Mymensingh- ۲۲۰۲, Bangladesh
M.L. Hossen
Department of Microbiology and Hygiene, Faculty of Veterinary Science, Bangladesh Agricultural University, Mymensingh- ۲۲۰۲, Bangladesh
M.A. Imran
Department of Microbiology and Hygiene, Faculty of Veterinary Science, Bangladesh Agricultural University, Mymensingh- ۲۲۰۲, Bangladesh