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The presence of viral subpopulations in an infectious bronchitis virus vaccine with differing pathogenicity – A preliminary study

There are currently four commercially available vaccines in Australia to protect chickens against infectious bronchitis virus (IBV). Predominantly, IBV causes clinical signs associated with respiratory or kidney disease, which subsequently cause an increase in mortality rate. Three of the current va...

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Autores principales: Hewson, Kylie A., Scott, Peter C., Devlin, Joanne M., Ignjatovic, Jagoda, Noormohammadi, Amir H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7115607/
https://www.ncbi.nlm.nih.gov/pubmed/22542436
http://dx.doi.org/10.1016/j.vaccine.2012.04.054
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author Hewson, Kylie A.
Scott, Peter C.
Devlin, Joanne M.
Ignjatovic, Jagoda
Noormohammadi, Amir H.
author_facet Hewson, Kylie A.
Scott, Peter C.
Devlin, Joanne M.
Ignjatovic, Jagoda
Noormohammadi, Amir H.
author_sort Hewson, Kylie A.
collection PubMed
description There are currently four commercially available vaccines in Australia to protect chickens against infectious bronchitis virus (IBV). Predominantly, IBV causes clinical signs associated with respiratory or kidney disease, which subsequently cause an increase in mortality rate. Three of the current vaccines belong to the same subgroup (subgroup 1), however, the VicS vaccine has been reported to cause an increased vaccinal reaction compared to the other subgroup 1 vaccines. Molecular anomalies detected in VicS suggested the presence of two major subspecies, VicS-v and VicS-del, present in the commercial preparation of VicS. The most notable anomaly is the absence of a 40 bp sequence in the 3′UTR of VicS-del. In this investigation, the two subspecies were isolated and shown to grow independently and to similar titres in embryonated chicken eggs. An in vivo investigation involved 5 groups of 20 chickens each and found that VicS-del grew to a significantly lesser extent in the chicken tissues collected than did VicS-v. The group inoculated with an even ratio of the isolated subspecies scored the most severe clinical signs, with the longest duration. These results indicate the potential for a cooperative, instead of an expected competitive, relationship between VicS-v and VicS-del to infect a host, which is reminiscent of RNA viral quasi-species.
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spelling pubmed-71156072020-04-02 The presence of viral subpopulations in an infectious bronchitis virus vaccine with differing pathogenicity – A preliminary study Hewson, Kylie A. Scott, Peter C. Devlin, Joanne M. Ignjatovic, Jagoda Noormohammadi, Amir H. Vaccine Article There are currently four commercially available vaccines in Australia to protect chickens against infectious bronchitis virus (IBV). Predominantly, IBV causes clinical signs associated with respiratory or kidney disease, which subsequently cause an increase in mortality rate. Three of the current vaccines belong to the same subgroup (subgroup 1), however, the VicS vaccine has been reported to cause an increased vaccinal reaction compared to the other subgroup 1 vaccines. Molecular anomalies detected in VicS suggested the presence of two major subspecies, VicS-v and VicS-del, present in the commercial preparation of VicS. The most notable anomaly is the absence of a 40 bp sequence in the 3′UTR of VicS-del. In this investigation, the two subspecies were isolated and shown to grow independently and to similar titres in embryonated chicken eggs. An in vivo investigation involved 5 groups of 20 chickens each and found that VicS-del grew to a significantly lesser extent in the chicken tissues collected than did VicS-v. The group inoculated with an even ratio of the isolated subspecies scored the most severe clinical signs, with the longest duration. These results indicate the potential for a cooperative, instead of an expected competitive, relationship between VicS-v and VicS-del to infect a host, which is reminiscent of RNA viral quasi-species. Elsevier Ltd. 2012-06-13 2012-04-26 /pmc/articles/PMC7115607/ /pubmed/22542436 http://dx.doi.org/10.1016/j.vaccine.2012.04.054 Text en Copyright © 2012 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Hewson, Kylie A.
Scott, Peter C.
Devlin, Joanne M.
Ignjatovic, Jagoda
Noormohammadi, Amir H.
The presence of viral subpopulations in an infectious bronchitis virus vaccine with differing pathogenicity – A preliminary study
title The presence of viral subpopulations in an infectious bronchitis virus vaccine with differing pathogenicity – A preliminary study
title_full The presence of viral subpopulations in an infectious bronchitis virus vaccine with differing pathogenicity – A preliminary study
title_fullStr The presence of viral subpopulations in an infectious bronchitis virus vaccine with differing pathogenicity – A preliminary study
title_full_unstemmed The presence of viral subpopulations in an infectious bronchitis virus vaccine with differing pathogenicity – A preliminary study
title_short The presence of viral subpopulations in an infectious bronchitis virus vaccine with differing pathogenicity – A preliminary study
title_sort presence of viral subpopulations in an infectious bronchitis virus vaccine with differing pathogenicity – a preliminary study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7115607/
https://www.ncbi.nlm.nih.gov/pubmed/22542436
http://dx.doi.org/10.1016/j.vaccine.2012.04.054
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