2020
DOI: 10.1007/s11262-020-01793-x
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Potential reverse spillover of infectious bursal disease virus at the interface of commercial poultry and wild birds

Abstract: Recently, multiple spillover events between domesticated poultry and wild birds have been reported for several avian viruses. This phenomenon highlights the importance of the livestock-wildlife interface in the possible emergence of novel viruses. The aim of the current study was to investigate the potential spillover and epidemiological links of infectious bursal disease virus (IBDV) between wild birds and domestic poultry. To this end, twenty-eight cloacal swabs were collected from four species of free-livin… Show more

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Cited by 4 publications
(12 citation statements)
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“…Indeed, recent studies have shown that when IBDV strains of two genotypes co-infect the same cell, their respective viral replication factories co-accumulate, thereby providing an opportunity for segment reassortment among the different genotypes ( 40 ). Recent studies have shown that wild birds can act as carriers of IBDV to transmit the virus to chickens ( 41 , 42 ), which might increase the risk of chickens infecting multiple genotypes of IBDV.…”
Section: Discussionmentioning
confidence: 99%
“…Indeed, recent studies have shown that when IBDV strains of two genotypes co-infect the same cell, their respective viral replication factories co-accumulate, thereby providing an opportunity for segment reassortment among the different genotypes ( 40 ). Recent studies have shown that wild birds can act as carriers of IBDV to transmit the virus to chickens ( 41 , 42 ), which might increase the risk of chickens infecting multiple genotypes of IBDV.…”
Section: Discussionmentioning
confidence: 99%
“…Naggar et al. (2020) and Jeon et al. (2008) both attempted viral isolation via chorioallantonic membrane (CAM) inoculation of embryonated specific pathogen free (SPF) chicken eggs.…”
Section: Resultsmentioning
confidence: 99%
“…Whereas the CAM harvested material in Naggar et al. (2020) was confirmed of IBDV isolation through a real‐time quantitative RT‐PCR (qRT‐PCR), Jeon et al. (2008) used both RT‐PCR and agar gel immunoprecipitation test (AGP) for confirmation.…”
Section: Resultsmentioning
confidence: 99%
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