Expression of Immunogenic S1 Gene of Infectious Bronchitis Virus from Field Outbreak in Eukaryotic Cells

2017 ◽  
Vol 7 (1) ◽  
pp. 27
Author(s):  
Sudhir Kumar Jain ◽  
Hemlata Jain ◽  
Megha Kadam Bedekar
1994 ◽  
Vol 34 (3) ◽  
pp. 327-338 ◽  
Author(s):  
Wang Li ◽  
Dave Junker ◽  
Lisa Hock ◽  
Elham Ebiary ◽  
Ellen W. Collisson

2016 ◽  
Vol 60 (3) ◽  
pp. 596-602 ◽  
Author(s):  
Huseyin Yilmaz ◽  
Eda Altan ◽  
Utku Y. Cizmecigil ◽  
Aydin Gurel ◽  
Gulay Yuzbasioglu Ozturk ◽  
...  

Vaccine ◽  
2003 ◽  
Vol 21 (21-22) ◽  
pp. 2730-2736 ◽  
Author(s):  
Michael A. Johnson ◽  
Catherine Pooley ◽  
Jagoda Ignjatovic ◽  
Scott G. Tyack

2013 ◽  
Vol 98 (4) ◽  
pp. 1727-1735 ◽  
Author(s):  
Yan-Quan Wei ◽  
Hui-Chen Guo ◽  
Hu Dong ◽  
Hai-Ming Wang ◽  
Jin Xu ◽  
...  

Virus Genes ◽  
2014 ◽  
Vol 49 (2) ◽  
pp. 292-303 ◽  
Author(s):  
Keyu Feng ◽  
Yu Xue ◽  
Feng Wang ◽  
Feng Chen ◽  
Dingming Shu ◽  
...  

2002 ◽  
Vol 46 (4) ◽  
pp. 831-838 ◽  
Author(s):  
Xiuqing Wang ◽  
William M. Schnitzlein ◽  
Deoki N. Tripathy ◽  
Theodore Girshick ◽  
Mazhar I. Khan

2019 ◽  
Vol 12 (3) ◽  
pp. 424-433 ◽  
Author(s):  
Musaed Abdulaziz Alsultan ◽  
Mohamed Ali Alhammadi ◽  
Maged Gomaa Hemida

Aim: This study aimed to isolate some of the currently circulating infectious bronchitis virus (IBV) strains from some broiler chicken farms in Al-Hasa and to do some molecular characteristics of these strains. Materials and Methods: We collected 300 tissue specimens, including the trachea, bronchi, lungs, and kidneys from some four commercial chicken farms showing respiratory manifestations. We tested these tissue specimens by the real-time polymerase chain reaction (RT-PCR) and gel-based PCR. We selected some PCR positive samples for isolation in the embryonated chicken eggs (ECE). We sequenced some PCR-positive samples and conducted phylogenetic analysis based on the obtained sequences. Results: Our molecular surveillance revealed that 31.6% of the tested specimens were IBV positive by PCR. We selected some positive specimens showing low Ct values by the qRT-PCR for virus isolation by the ECE. The infected eggs showed hemorrhage, dwarfing, and death in some cases after three passages in the ECE. We sequenced some of the positive PCR specimens and used the obtained sequences to draw the phylogenetic tree based on the partial IBV-ORF-1a, N, and S1 gene sequences. The phylogenetic trees based on the IBV-N and S1 gene sequences showed that the circulating IBV strains in Al-Hasa during 2016 was showing a high degree of identity to some strains from Taiwan and Italy. Meanwhile, the grouping of these strains based on the IBV-S1 sequences revealed that the currently circulating IBV strains in Al-Hasa belonged to Gr.I.7 along with strains from Taiwan. Conclusion: Our results confirmed the continuous circulation of the IBV among the chicken population in Al-Hasa despite the intensive application of vaccines against this virus.


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