Characterization of Nephropathogenic Infectious Bronchitis Virus DMV/1639/11 Recovered from Delmarva Broiler Chickens in 2011
Authors:
- Jack GelbJGJack Gelb
- Brian S. LadmanBLBrian S. Ladman
- Conrad R. PopeCPConrad R. Pope
- J. Miguel RuanoJRJ. Miguel Ruano
- Erin M. BrannickEBErin M. Brannick
- Daniel A. BautistaDBDaniel A. Bautista
- Colleen M. CoughlinCCColleen M. Coughlin
- Lauren A. PreskenisLPLauren A. Preskenis
- 1 March 2013
- journal article
- Published by American Association of Avian Pathologists (AAAP) in Avian Diseases
- Vol. 57 (1) , 65-70
Abstract
A limited outbreak of nephropathogenic infectious bronchitis (NIB) occurred in three Delmarva (DMV) commercial broiler chicken flocks in 2011. Isolates of NIB virus (NIBV)--DMV/1639/11, DMV/3432/11, and DMV/3902/11--were characterized by sequence analysis of the N-terminal subunit (S1) of the spike (S) gene. Findings indicated that the isolates were identical to each other and to PA/9579A/10, a 2010 isolate from poultry in Pennsylvania. The 2010 and 2011 isolates appear to have originated from a 1997-2000 NIB outbreak in Pennsylvania. DMV/1639/11 and PA/9579A/10 were determined to be nephropathogenic in susceptible chickens, yielding virus reisolations from kidney and inducing characteristic interstitial nephritis microscopic lesions. In a controlled laboratory study, 40% of chickens vaccinated with a combination live vaccine containing infectious bronchitis virus (IBV) strains Massachusetts (Mass) + Connecticut (Conn) were positive on virus isolation attempts after challenge with DMV/1639/11, compared with only 13% of Mass + Arkansas (Ark) vaccinates. Both combination vaccines gave partial protection against the development of DMV/1639/11-induced renal lesions. Although numerically fewer chickens vaccinated with Mass + Conn had interstitial nephritis compared with those vaccinated with Mass + Ark, neither vaccine combination offered greater protection (P < 0.05) than observed in unvaccinated chickens challenged with DMV/1639/11. Mass + Ark vaccinations, applied under commercial conditions in the hatchery (spray) and on-farm (spray), did not protect the trachea or kidney from DMV/1639/11 challenge. Serologic testing of broiler flocks found < 3% (2 of 69) tested to possess specific antibodies to DMV/1639/11, indicating the virus had not become established in the region.Keywords
This publication has 17 references indexed in Scilit:
- Genotyping of Newly Isolated Infectious Bronchitis Virus Isolates from Northeastern GeorgiaAvian Diseases, 2010
- Infectious Bronchitis Virus Field Vaccination Coverage and Persistence of Arkansas-Type Viruses in Commercial BroilersAvian Diseases, 2009
- Pathogenicity and antigenicity of a new variant of Korean nephropathogenic infectious bronchitis virusJournal of Veterinary Science, 2009
- Different genotypes of nephropathogenic infectious bronchitis viruses co-circulating in chicken population in ChinaVirus Genes, 2007
- Development and evaluation of a real-time Taqman RT-PCR assay for the detection of infectious bronchitis virus from infected chickensJournal of Virological Methods, 2006
- S1 gene sequence analysis of a nephropathogenic strain of avian infectious bronchitis virus in EgyptVirology Journal, 2006
- Protection of Chickens After Live and Inactivated Virus Vaccination Against Challenge with Nephropathogenic Infectious Bronchitis Virus PA/Wolgemuth/98Avian Diseases, 2002
- Novel Infectious Bronchitis Virus S1 Genotypes in Mexico 1998-19992001
- A Rapid-Plate Hemagglutination Assay for the Detection of Infectious Bronchitis Virus2000
- Isolation, characterisation and preliminary cross‐protection studies with a new pathogenic avian infectious bronchitis virus (Strain PL‐84084)Avian Pathology, 1986