Literature DB >> 31928697

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.

Md Ahaduzzaman1, Peter J Groves2, Sue M Sharpe3, Sarah L Williamson3, Yuanshuo K Gao4, Trong V Nguyen5, Priscilla F Gerber6, Stephen W Walkden-Brown6.   

Abstract

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.
Copyright © 2019 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Dust sampling; ILTV; Shedding profile; Vaccine monitoring; qPCR

Year:  2019        PMID: 31928697     DOI: 10.1016/j.vetmic.2019.108545

Source DB:  PubMed          Journal:  Vet Microbiol        ISSN: 0378-1135            Impact factor:   3.293


  5 in total

1.  Characterization of poultry house dust using chemometrics and scanning electron microscopy imaging.

Authors:  Md Ahaduzzaman; Luke Milan; Christine L Morton; Priscilla F Gerber; Stephen W Walkden-Brown
Journal:  Poult Sci       Date:  2021-04-20       Impact factor: 3.352

2.  Methods to prevent PCR amplification of DNA from non-viable virus were not successful for infectious laryngotracheitis virus.

Authors:  Yugal Raj Bindari; Stephen W Walkden-Brown; Priscilla F Gerber
Journal:  PLoS One       Date:  2020-05-22       Impact factor: 3.240

3.  Indicators and risk factors of infectious laryngotracheitis in layer hen flocks in Algeria.

Authors:  Omar Salhi; Chafik Redha Messaï; Nassim Ouchene; Iman Boussaadi; Hassiba Kentouche; Rachid Kaidi; Djamel Khelef
Journal:  Vet World       Date:  2021-01-22

4.  Transmission of infectious laryngotracheitis virus vaccine and field strains: the role of degree of contact and transmission by whole blood, plasma and poultry dust.

Authors:  Addisu A Yegoraw; Awol M Assen; Priscilla F Gerber; Stephen W Walkden-Brown
Journal:  Vet Res       Date:  2021-06-22       Impact factor: 3.683

5.  Microbial communities of poultry house dust, excreta and litter are partially representative of microbiota of chicken caecum and ileum.

Authors:  Yugal R Bindari; Robert J Moore; Thi Thu Hao Van; Matthew Hilliar; Shu-Biao Wu; Stephen W Walkden-Brown; Priscilla F Gerber
Journal:  PLoS One       Date:  2021-08-05       Impact factor: 3.240

  5 in total

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