Literature DB >> 29077954

Evaluation of 793/B-like and Mass-like vaccine strain kinetics in experimental and field conditions by real-time RT-PCR quantification.

C M Tucciarone1, G Franzo1, G Berto2, M Drigo1, G Ramon3, K C Koutoulis4, E Catelli5, M Cecchinato1.   

Abstract

Infectious bronchitis virus (IBV) is a great economic burden both for productive losses and costs of the control strategies. Many different vaccination protocols are applied in the same region and even in consecutive cycles on the same farm in order to find the perfect balance between costs and benefits. In Northern Italy, the usual second vaccination is more and more often moved up to the chick's first d of life. The second strain administration together with the common Mass priming by spray at the hatchery allows saving money and time and reducing animal stress. The present work compared the different vaccine strains (Mass-like or B48, and 1/96) kinetics both in field conditions and in a 21-day-long experimental trial in broilers, monitoring the viral replication by upper respiratory tract swabbing and vaccine specific real time reverse transcription PCR (RT-PCR) quantification. In both field and experimental conditions, titers for all the vaccines showed an increasing trend in the first 2 wk and then a decrease, though still remaining detectable during the whole monitored period. IBV field strain and avian Metapneumovirus (aMPV) presence also was also investigated by RT-PCR and sequencing, and by multiplex real-time RT-PCR, respectively, revealing a consistency in the pathogen introduction timing at around 30 d, in correspondence with the vaccine titer's main decrease. These findings suggest the need for an accurate knowledge of live vaccine kinetics, whose replication can compete with the other pathogen one, providing additional protection to be added to what is conferred by the adaptive immune response.
© 2017 Poultry Science Association Inc.

Entities:  

Keywords:  infectious bronchitis virus; protectotype; quantification; vaccination

Mesh:

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Year:  2018        PMID: 29077954     DOI: 10.3382/ps/pex292

Source DB:  PubMed          Journal:  Poult Sci        ISSN: 0032-5791            Impact factor:   3.352


  4 in total

1.  A closed-tube, single-step, real time, reverse transcription-loop-mediated isothermal amplification assay for infectious bronchitis virus detection in chickens.

Authors:  Mohamed El-Tholoth; Michael G Mauk; Eman Anis; Haim H Bau
Journal:  J Virol Methods       Date:  2020-07-17       Impact factor: 2.014

2.  Vaccine or field strains: the jigsaw pattern of infectious bronchitis virus molecular epidemiology in Poland.

Authors:  Matteo Legnardi; Giovanni Franzo; Konstantinos C Koutoulis; Marek Wiśniewski; Elena Catelli; Claudia Maria Tucciarone; Mattia Cecchinato
Journal:  Poult Sci       Date:  2019-12-01       Impact factor: 3.352

3.  Metagenomic sequencing determines complete infectious bronchitis virus (avian Gammacoronavirus) vaccine strain genomes and associated viromes in chicken clinical samples.

Authors:  Steven Van Borm; Mieke Steensels; Elisabeth Mathijs; Frank Vandenbussche; Thierry van den Berg; Bénédicte Lambrecht
Journal:  Virus Genes       Date:  2021-10-09       Impact factor: 2.332

4.  Evaluation of UVC Excimer Lamp (222 nm) Efficacy for Coronavirus Inactivation in an Animal Model.

Authors:  Claudia Maria Tucciarone; Mattia Cecchinato; Lucrezia Vianello; Gabriele Simi; Enrico Borsato; Luca Silvestrin; Michele Giorato; Cristiano Salata; Mauro Morandin; Elisa Greggio; Michele Drigo
Journal:  Viruses       Date:  2022-09-14       Impact factor: 5.818

  4 in total

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