2017
DOI: 10.1016/j.jviromet.2017.02.018
|View full text |Cite
|
Sign up to set email alerts
|

New real time and conventional RT-PCRs for updated molecular diagnosis of infectious bronchitis virus infection (IBV) in chickens in Egypt associated with frequent co-infections with avian influenza and Newcastle Disease viruses

Abstract: In Egypt, currently two geographically restricted genotypes of the infectious bronchitis coronavirus (IBV) are circulating with detrimental effects for poultry industry. A sensitive real-time RT-PCR assay targeting the IBV nucleocapsid gene (N) was developed to screen clinical samples for presence of IBV. Conventional RT-PCRs amplifying hypervariable regions (HVRs 1-2 and 3) of the IBV S1 gene were developed and amplificates used for nucleotide sequence-based typing of IBV field strains in Egyptian chickens di… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

1
43
0
1

Year Published

2017
2017
2024
2024

Publication Types

Select...
7

Relationship

2
5

Authors

Journals

citations
Cited by 34 publications
(49 citation statements)
references
References 42 publications
1
43
0
1
Order By: Relevance
“…The likelihood of the importance of these scenarios is low, as the cocirculation of both viruses on the same poultry farms at the same time, the coinfection of chickens with both viruses, and the presence of both viruses in the same poultry field samples have been repeatedly reported (27)(28)(29), However, the emergence and perpetuation of the now extinct HPAIV H5N1 2.2.1.1 clade of vaccine escape mutants from 2008 to 2011 were highly restricted to industrial poultry farms. These viruses did not spill over to backyard holdings, where viruses of another clade (2.2.1.2) prevailed (25).…”
Section: Discussionmentioning
confidence: 99%
“…The likelihood of the importance of these scenarios is low, as the cocirculation of both viruses on the same poultry farms at the same time, the coinfection of chickens with both viruses, and the presence of both viruses in the same poultry field samples have been repeatedly reported (27)(28)(29), However, the emergence and perpetuation of the now extinct HPAIV H5N1 2.2.1.1 clade of vaccine escape mutants from 2008 to 2011 were highly restricted to industrial poultry farms. These viruses did not spill over to backyard holdings, where viruses of another clade (2.2.1.2) prevailed (25).…”
Section: Discussionmentioning
confidence: 99%
“…Chicks infected with IBV then super-infected with AIV-3 days later, showed no IBV shedding either in TC or CL, during the experimental period (Figs. [2][3][4][5]. When comparing the kinetics of AIV or IBV virus replication at different time points after chick inoculations, the patterns of TC and CL viral titers were different depending on the virus exposure, as shown for AIV or IBV viral gene copy numbers detected by qRT-PCR ( Figs.…”
Section: Single Infectionsmentioning
confidence: 89%
“…Mixed infection or co-infection with AIV and IBV has been described as a natural infection in different countries in Asia and the Middle-East [2,3]. More, the IBV vaccine is used extensively in chicken farms in many countries worldwide where both IBV and low pathogenic AIV H9N2 are endemic [3,4]. The H120 strain of IBV was one of the earliest live attenuated IBV vaccines to be developed and has continued to be use in most parts of the world.…”
Section: Introductionmentioning
confidence: 99%
“…Viral RNA was extracted using the QIAamp viral RNA mini kit (QIAGEN) in accordance with the manufacturer instructions. One-step RT-PCR was performed for IBV screening as previously described [17]. Genotyping with forward and reverse primers for amplification of HVR1, amplicon purification and sequencing was performed as previously described [17].…”
Section: Ibv and Ecoli Detection And Characterizationmentioning
confidence: 99%
“…One-step RT-PCR was performed for IBV screening as previously described [17]. Genotyping with forward and reverse primers for amplification of HVR1, amplicon purification and sequencing was performed as previously described [17]. Obtained sequences in this study aligned with sequences represent all infectious bronchitis virus genotypes proposed by [18].…”
Section: Ibv and Ecoli Detection And Characterizationmentioning
confidence: 99%