Abstract

This study assessed different methods (tracheal and choanal cleft swabs from individual birds, and poultry dust as a population level measure) to evaluate the shedding kinetics of infectious bronchitis virus (IBV) and Newcastle disease virus (NDV) genome in meat chicken flocks after spray vaccination at hatchery. Dust samples and tracheal and choanal cleft swabs were collected from four meat chicken flocks at 10, 14, 21 and 31 days post vaccination (dpv) and tested for IBV and NDV genome copies (GC) by reverse transcriptase (RT)-PCR. IBV and NDV GC were detected in all sample types throughout the study period. Detection rates for choanal cleft and tracheal swabs were comparable, with moderate and fair agreement between sample types for IBV (McNemar’s = 0.27, kappa = 0.44) and NDV (McNemar’s = 0.09; kappa = 0.31) GC respectively. There was no significant association for IBV GC in swabs and dust samples (R2 = 0.15, P = 0.13) but NDV detection rates and viral load in swabs were strongly associated with NDV GC in dust samples (R2 = 0.86 and R2 = 0.90, P<0.001). There was no difference in IBV and NDV GC in dust samples collected from different locations within a poultry house. In conclusion, dust samples collected from any location within poultry house show promise for monitoring IBV and NDV GC in meat chickens at a population level and choanal cleft swabs can be used for detection of IBV and NDV GC instead of tracheal swabs in individual birds.

Highlights

  • Infectious bronchitis (IB) and Newcastle disease (ND) are highly transmissible diseases that cause substantial economic losses in the poultry industry [1, 2]

  • infectious bronchitis virus (IBV) and Newcastle disease virus (NDV) genome copies (GC) detection rates and viral load at different days post vaccination in tracheal and choanal cleft swabs, and dust samples are summarised in Tables 1 and 2

  • Detection rate and load of IBV and NDV genomes following spray vaccination at hatchery in meat chickens grown in tunnel ventilated houses can be determined using tracheal and choanal cleft swabs, and dust samples

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Summary

Introduction

Infectious bronchitis (IB) and Newcastle disease (ND) are highly transmissible diseases that cause substantial economic losses in the poultry industry [1, 2]. Infectious bronchitis is caused by infectious bronchitis virus (IBV), a gammacoronavirus with a single-stranded positive sense RNA genome [3]. Newcastle disease is caused by virulent strains of Newcastle disease. NDV and IBV detection in chicken swabs and poultry dust study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of these authors are articulated in the ‘author contributions’ section

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