A practical method for assessing infectious laryngotracheitis vaccine take in broilers following mass administration in water: Spatial and temporal variation in viral genome content of poultry dust after vaccination
| Autor: | Sue M. Sharpe, Trong Van Nguyen, Peter J. Groves, Priscilla F. Gerber, Stephen W. Walkden-Brown, Sarah L. Williamson, Yuanshuo K. Gao, Md. Ahaduzzaman |
|---|---|
| Rok vydání: | 2019 |
| Předmět: |
Veterinary medicine
Genome Viral Biology Infectious laryngotracheitis Real-Time Polymerase Chain Reaction Microbiology Genome Mass Vaccination law.invention 03 medical and health sciences Herpesvirus 1 Gallid law Animals Polymerase chain reaction Poultry Diseases 030304 developmental biology 0303 health sciences Attenuated vaccine General Veterinary 030306 microbiology Outbreak Dust Viral Vaccines General Medicine Herpesviridae Infections Housing Animal Vaccination DNA Viral Mass vaccination Flock New South Wales Chickens |
| Zdroj: | Veterinary microbiology. 241 |
| ISSN: | 1873-2542 |
| Popis: | Infectious laryngotracheitis is an important disease of chickens caused by infectious laryngotracheitis virus (ILTV). Outbreaks commonly occur in meat chicken flocks and mass vaccination with live attenuated vaccines, usually in water, is used to control the disease in these populations. Vaccination with live virus via water and nipple drinkers requires stringent adherence to protocols to ensure success, but vaccine administration monitoring is not currently assessed due to a lack of economically viable methods. Vaccinal ILTV has been shown to be detectable in dust in experimental studies and has potential as a method of assessing vaccination success. However, the pattern of vaccinal ILTV detection in dust following vaccination under commercial conditions has not been defined. We report the longitudinal profile of ILTV genome copies (GC) in poultry house dust collected on settle plates following vaccination of 8 flocks of commercial meat chickens on four farms. ILTV GC was enumerated using quantitative real-time polymerase chain reaction (qPCR). There was considerable variation between flocks in the levels of ILTV GC detected post vaccination and this variation was significantly associated with vaccine take measured in individual birds in a companion study. There was no effect of sampling location on ILTV GC in dust but the amount of dust collected was greater in locations closer to the exhaust fans in artificially ventilated houses. Results indicate that measurement of ILTV GC in single or pooled dust samples at 7-8 days post vaccination enables detection of poor vaccine takes and provides a practical means of monitoring ILT vaccination. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|
Full Text from ScienceDirect