Literature DB >> 24689182

Evaluation of infectious bronchitis virus Arkansas-type vaccine failure in commercial broilers.

Ha-Jung Roh, Deborah A Hilt, Susan M Williams, Mark W Jackwooda.   

Abstract

Infectious bronchitis virus (IBV) causes an upper respiratory tract disease in chickens and is highly contagious. Many different types of the virus exist, but only a few types are used as attenuated live vaccines in the commercial poultry industry. Of the vaccine types used, the Arkansas (Ark)-type virus is most frequently reisolated from vaccinated broilers. Previous research has suggested that incomplete clearance of Ark-type vaccine virus plays a role in the inadequate protection observed when vaccinated broilers are challenged with pathogenic Ark virus. In this study, we examine routes of vaccine administration using multiple IBV types including Ark in an effort to understand why Ark vaccines do not provide good protection and persist in commercial broilers. We found that interference between different types of IBV vaccines was not occurring when combined and administered using a commercial hatchery spray cabinet. Also, Ark vaccine virus was not efficacious in 1-day-old broilers when sprayed using a hatchery spray cabinet, but it gave good protection when administrated by eyedrop inoculation. We also found that the amount of Ark vaccine virus was low or undetectable in choanal swabs out to 35 days postvaccination when vaccine was administered by eyedrop or drinking water. Alternatively, a subpopulation of the Ark vaccine isolated from a vaccinated bird, Ark-RI-EP1, showed a peak titer at 7-10 days of age when given by the same routes, suggesting that the Ark-RI-EP1 was more fit with regard to infection, replication in the birds, or both. Moreover, we found that detection of IBV vaccine virus early after administration, regardless of strain or route, correlated with protection against homologous challenge and may thus be a good indicator of vaccine efficacy in the field because humoral antibody titers are typically low or undetectable after vaccination. These experiments provided key findings that can be used to direct efforts for improving the efficacy of IBV Ark-type vaccines given in the hatchery. They also elucidated factors contributing to the persistence of Ark vaccine in the field.

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Year:  2013        PMID: 24689182     DOI: 10.1637/10459-112812-Reg.1

Source DB:  PubMed          Journal:  Avian Dis        ISSN: 0005-2086            Impact factor:   1.577


  12 in total

1.  Transcriptome analysis of primary chicken cells infected with infectious bronchitis virus strain K047-12 isolated in Korea.

Authors:  Rangyeon Lee; Ji Seung Jung; Ji-In Yeo; Hyuk Moo Kwon; Jeongho Park
Journal:  Arch Virol       Date:  2021-06-05       Impact factor: 2.685

2.  Molecular characterization and phylogenetic analyses of virulent infectious bronchitis viruses isolated from chickens in Eastern Saudi Arabia.

Authors:  Maged Gomaa Hemida; Mohammed A Al-Hammadi; Abdul Hafeed S Daleb; Cecilio R Gonsalves
Journal:  Virusdisease       Date:  2017-05-09

3.  Different evolutionary trajectories of vaccine-controlled and non-controlled avian infectious bronchitis viruses in commercial poultry.

Authors:  Mark W Jackwood; Dong-Hun Lee
Journal:  PLoS One       Date:  2017-05-04       Impact factor: 3.240

4.  Effect of Pullet Vaccination on Development and Longevity of Immunity.

Authors:  Emily J Aston; Brian J Jordan; Susan M Williams; Maricarmen García; Mark W Jackwood
Journal:  Viruses       Date:  2019-02-02       Impact factor: 5.048

5.  Insights from molecular structure predictions of the infectious bronchitis virus S1 spike glycoprotein.

Authors:  Christina Lora M Leyson; Brian J Jordan; Mark W Jackwood
Journal:  Infect Genet Evol       Date:  2016-11-09       Impact factor: 3.342

6.  Specific detection of GII-1 lineage of infectious bronchitis virus.

Authors:  K Domanska-Blicharz; A Lisowska; A Pikuła; J Sajewicz-Krukowska
Journal:  Lett Appl Microbiol       Date:  2017-07-03       Impact factor: 2.858

7.  Biological and molecular characterization of ArkGA: A novel Arkansas serotype vaccine that is highly attenuated, efficacious, and protective against homologous challenge.

Authors:  Grace A Albanese; Dong-Hun Lee; I-Hsin N Cheng; Deborah A Hilt; Mark W Jackwood; Brian J Jordan
Journal:  Vaccine       Date:  2018-09-07       Impact factor: 3.641

8.  Polymorphisms in the S1 spike glycoprotein of Arkansas-type infectious bronchitis virus (IBV) show differential binding to host tissues and altered antigenicity.

Authors:  Christina Leyson; Monique França; Mark Jackwood; Brian Jordan
Journal:  Virology       Date:  2016-09-15       Impact factor: 3.616

9.  Validation of specific quantitative real-time RT-PCR assay panel for Infectious Bronchitis using synthetic DNA standards and clinical specimens.

Authors:  Jongseo Mo; Michael Angelichio; Lisa Gow; Valerie Leathers; Mark W Jackwood
Journal:  J Virol Methods       Date:  2019-11-08       Impact factor: 2.014

10.  Molecular survey and interaction of common respiratory pathogens in chicken flocks (field perspective).

Authors:  Adel M Abdelaziz; Mahmoud H A Mohamed; Mahmoud M Fayez; Theeb Al-Marri; Ibrahim Qasim; Abdul Aziz Al-Amer
Journal:  Vet World       Date:  2019-12-16
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