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Sequence diversity and evolution of infectious bursal disease virus in Iraq

Background: Infectious Bursal Disease (IBD) is a highly infectious disease which causes huge economic losses to the poultry industry due to the direct impact of the illness and indirect consequences such as decreasing the general immunity of the flock, leaving it naive to other diseases. In Iraq, IB...

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Autores principales: Abbas, Ali Hadi, AL saegh, Haider Abas, ALaraji, Furkan Sabbar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8436185/
https://www.ncbi.nlm.nih.gov/pubmed/34646501
http://dx.doi.org/10.12688/f1000research.28421.2
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author Abbas, Ali Hadi
AL saegh, Haider Abas
ALaraji, Furkan Sabbar
author_facet Abbas, Ali Hadi
AL saegh, Haider Abas
ALaraji, Furkan Sabbar
author_sort Abbas, Ali Hadi
collection PubMed
description Background: Infectious Bursal Disease (IBD) is a highly infectious disease which causes huge economic losses to the poultry industry due to the direct impact of the illness and indirect consequences such as decreasing the general immunity of the flock, leaving it naive to other diseases. In Iraq, IBD is highly prevalent despite vaccination programs, yet studies on sequence diversity of the causative virus are still rare.  Methods: A sample from Bursa of Fabricius from an IBD outbreak in a flock in the city of Najaf in Iraq was smeared on an FTA card. Amplicons of targeted regions in VP1 and VP2 genes were generated and sequenced. Sequences were then compared with other local and global sequences downloaded from GenBank repositories. Sequence alignment and DNA sequence analyses were achieved using MUSCLE, UGENE and MEGAx software. The molecular clock and sequence evolutionary analyses were applied using MEGAx tools.  Results: The strain sequenced in this study belongs to a very virulent Infectious Bursal Disease Virus (vvIBDV) as the DNA and phylogenetic analysis of VP1 and VP2 gene sequences showed a mutual clustering with similar sequences belonging to vvIBDV genogroup 3. Analyses of the hyper variable region of VP2 gene (hvVP2) of IBDV isolates from Iraq indicates a presence of sequence diversity. Interestingly, the two vaccine strains Ventri IBDV Plus and ABIC MB71 that showed the highest sequence similarity to the local isolates in the hvVP2 region are not used in vaccination routine against IBDV in Iraq.  Conclusion: Sequences of vvIBDV in Iraq are diverse. Remarkably, some of the available vaccine strains show high sequence similarity with local strains in Iraq; however, they are not included in the routine vaccination programs. Analysis of more samples involving more geographical regions is needed to draw a detailed map of antigenic diversity of IBDV in Iraq.
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spelling pubmed-84361852021-10-12 Sequence diversity and evolution of infectious bursal disease virus in Iraq Abbas, Ali Hadi AL saegh, Haider Abas ALaraji, Furkan Sabbar F1000Res Research Article Background: Infectious Bursal Disease (IBD) is a highly infectious disease which causes huge economic losses to the poultry industry due to the direct impact of the illness and indirect consequences such as decreasing the general immunity of the flock, leaving it naive to other diseases. In Iraq, IBD is highly prevalent despite vaccination programs, yet studies on sequence diversity of the causative virus are still rare.  Methods: A sample from Bursa of Fabricius from an IBD outbreak in a flock in the city of Najaf in Iraq was smeared on an FTA card. Amplicons of targeted regions in VP1 and VP2 genes were generated and sequenced. Sequences were then compared with other local and global sequences downloaded from GenBank repositories. Sequence alignment and DNA sequence analyses were achieved using MUSCLE, UGENE and MEGAx software. The molecular clock and sequence evolutionary analyses were applied using MEGAx tools.  Results: The strain sequenced in this study belongs to a very virulent Infectious Bursal Disease Virus (vvIBDV) as the DNA and phylogenetic analysis of VP1 and VP2 gene sequences showed a mutual clustering with similar sequences belonging to vvIBDV genogroup 3. Analyses of the hyper variable region of VP2 gene (hvVP2) of IBDV isolates from Iraq indicates a presence of sequence diversity. Interestingly, the two vaccine strains Ventri IBDV Plus and ABIC MB71 that showed the highest sequence similarity to the local isolates in the hvVP2 region are not used in vaccination routine against IBDV in Iraq.  Conclusion: Sequences of vvIBDV in Iraq are diverse. Remarkably, some of the available vaccine strains show high sequence similarity with local strains in Iraq; however, they are not included in the routine vaccination programs. Analysis of more samples involving more geographical regions is needed to draw a detailed map of antigenic diversity of IBDV in Iraq. F1000 Research Limited 2021-09-02 /pmc/articles/PMC8436185/ /pubmed/34646501 http://dx.doi.org/10.12688/f1000research.28421.2 Text en Copyright: © 2021 Abbas AH et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Abbas, Ali Hadi
AL saegh, Haider Abas
ALaraji, Furkan Sabbar
Sequence diversity and evolution of infectious bursal disease virus in Iraq
title Sequence diversity and evolution of infectious bursal disease virus in Iraq
title_full Sequence diversity and evolution of infectious bursal disease virus in Iraq
title_fullStr Sequence diversity and evolution of infectious bursal disease virus in Iraq
title_full_unstemmed Sequence diversity and evolution of infectious bursal disease virus in Iraq
title_short Sequence diversity and evolution of infectious bursal disease virus in Iraq
title_sort sequence diversity and evolution of infectious bursal disease virus in iraq
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8436185/
https://www.ncbi.nlm.nih.gov/pubmed/34646501
http://dx.doi.org/10.12688/f1000research.28421.2
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