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2016
DOI: 10.1016/j.jviromet.2016.05.007
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Development of RT-qPCR assays for the specific identification of two major genotypes of avian infectious bronchitis virus

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Cited by 10 publications
(8 citation statements)
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“…To rapidly enact appropriate control measures to contain the infection, real time, molecular detection methods are needed to test samples from chickens suspected of being infected in proximity to poultry farms. In resource-rich settings, this task is accomplished with single-step-real-time RT-PCR assays for IB detection, genotyping, and discrimination between vaccine and pathogenic strains ( Fraga et al, 2016 ; Marandino et al, 2016 ; Domanska-Blicharz et al, 2017 ; Stenzel et al, 2017 ; Tucciarone et al, 2018 ).…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…To rapidly enact appropriate control measures to contain the infection, real time, molecular detection methods are needed to test samples from chickens suspected of being infected in proximity to poultry farms. In resource-rich settings, this task is accomplished with single-step-real-time RT-PCR assays for IB detection, genotyping, and discrimination between vaccine and pathogenic strains ( Fraga et al, 2016 ; Marandino et al, 2016 ; Domanska-Blicharz et al, 2017 ; Stenzel et al, 2017 ; Tucciarone et al, 2018 ).…”
Section: Discussionmentioning
confidence: 99%
“…Current field diagnosis of IB relies on clinical signs and post-mortem lesions examination that are not pathognomonic and require confirmatory laboratory testing. Confirmative virus detection is carried out in centralized laboratories by virus isolation (VI), virus neutralization (VN) test, enzyme-linked immunosorbant assay (ELISA), haemagglutination inhibition (HI) ( Cooke et al, 1987 ; Cavanagh, 2007 ; Jackwood and de Wit, 2013 ; Pradhan et al, 2014 ; Ding et al, 2015 ), conventional RT-PCR, and quantitative RT-PCR (RT-qPCR) ( Callison et al, 2006 ; Meir et al, 2010 ; Fraga et al, 2016 ; Marandino et al, 2016 ; Fellahi et al, 2016 ; Laamiri et al, 2018 ; Molenaar et al, 2020 ). However, the aforementioned diagnostic methods pose challenges for implementing rapid, specific and simple detection in rudimentary veterinary diagnostic laboratories, particularly in resource-poor settings.…”
Section: Introductionmentioning
confidence: 99%
“…Certain RT-PCR tests can also distinguish types of viruses, i.e., they are vaccine-related or field-related which helps to match their genetic sequences for better vaccination plans. Avian mycoplasmosis, infectious laryngotracheitis, Newcastle disease and avian influenza have similar clinical signs like infectious bronchitis, so preventive measures should be taken to differentiate appropriately [48][49][50][51][52][53][54]. Now vaccine-related viruses and pathogenic viruses can be screened.…”
Section: Molecular Diagnosticsmentioning
confidence: 99%
“…A multitude of RT-PCR and qRT-PCR-based methods have been validated, either generic and targeting virtually all IBV subtypes, or genotype- or strain-specific [ 64 , 65 , 66 , 67 , 68 ]. The most commonly targeted region is the S1 gene, where the genetic variability featuring IBV variants is concentrated [ 3 ].…”
Section: Approaches To Ibv Diagnosismentioning
confidence: 99%